Transferrin receptor binding proteins and conjugates

Abstract

Provided herein are proteins comprising one monovalent human TfR binding domain ("human TfR binding proteins"), conjugates comprising such human TfR binding proteins, e.g., human TfR binding proteins-dsRNA conjugates, pharmaceutical compositions comprising human TfR binding proteins or conjugates, and methods of treating CNS diseases (e.g., neurodegenerative disease such as neurodegenerative synucleinopathy or tauopathy) using human TfR binding proteins or conjugates.

Description

TRANSFERRIN RECEPTOR BINDING PROTEINS AND CONJUGATES SEQUENCE LISTING

[0001] The present application is being filed along with a Sequence Listing in ST.26 XML format. The Sequence Listing is provided as a file titled “30822_WO” created 26-August-2024 and is 422 kilobytes in size. The Sequence Listing information in the ST.26 XML format is incorporated herein by reference in its entirety. BACKGROUND

[0002] The blood brain barrier (BBB) is a selective semipermeable border of capillary endothelial cells that prevents solutes, including pathogens, from passing into the central nervous system (CNS). The BBB allows the passage of some small molecules by passive diffusion and the cells of BBB actively transport metabolic products crucial to neural function such as glucose and amino acids across the barrier using specific transport proteins. The BBB has neuroprotective function by tightly controlling access to the brain; but it also impedes access of therapeutic agents to CNS.

[0003] BBB shuttles for improving passage of the therapeutic agents across the blood brain barrier and into the CNS have been described. For example, WO2003 / 009815 describes the use of antibodies directed to transferrin receptor (“TfR”) for modulating blood brain barrier transport and delivering therapeutic agents across BBB. However, attempts at using anti-TfR antibodies to shuttle therapeutic agents across the BBB have proven challenging. To date, there are no approved TfR shuttles or conjugates for the treatment of CNS diseases in the U.S.

[0004] RNA interference (RNAi) is a highly conserved regulatory mechanism in which RNA molecules are involved in sequence-specific suppression of gene expression by double-stranded RNA molecules (dsRNA) (Fire et al., Nature 391:806-811, 1998).

[0005] Therefore, there remains a need for TfR binding proteins and conjugates that can deliver therapeutic agents, e.g., RNAi agent, across the BBB into the CNS for the treatment of various CNS diseases. SUMMARY OF INVENTION

[0006] Provided herein are proteins comprising one monovalent human TfR binding domain (“human TfR binding proteins”), conjugates comprising such human TfR binding proteins, e.g.,human TfR binding proteins-dsRNA conjugates, pharmaceutical compositions comprising human TfR binding proteins or conjugates, and methods of treating CNS diseases (e.g., neurodegenerative disease such as neurodegenerative synucleinopathy or tauopathy) using human TfR binding proteins or conjugates. The conjugates comprising human TfR binding proteins provided herein have improved yield and / or reduced microheterogeneity.

[0007] In one aspect, provided herein are proteins comprising one monovalent human TfR binding domain (“human TfR binding proteins”).

[0008] In some embodiments, the human TfR binding protein is any one of the human TfR binding proteins in Table 1b.

[0009] In some embodiments, provided herein are proteins comprising one monovalent human transferrin receptor (TfR) binding domain, wherein the protein comprises two heavy chains HC1 and HC2 and one light chain LC1, and wherein the HC1, HC2 and LC1 comprise the following sequences: (a) HC1 comprises SEQ ID NO: 11, LC1 comprises SEQ ID NO: 10, HC2 comprises SEQ ID NO: 12, or (b) HC1 comprises SEQ ID NO: 13, LC1 comprises SEQ ID NO: 10, HC2 comprises SEQ ID NO: 14.

[0010] In some embodiments, the human TfR binding protein has a one arm heteromab format. In some embodiments, the human TfR binding protein comprises two heavy chains HC1 and HC2 and one light chain LC1, wherein HC1 comprises SEQ ID NO: 11, LC1 comprises SEQ ID NO: 10, HC2 comprises SEQ ID NO: 12. In some embodiments, provided herein are human TfR binding proteins comprise two heavy chains HC1 and HC2 and one light chain LC1, wherein HC1 comprises SEQ ID NO: 13, LC1 comprises SEQ ID NO: 10, HC2 comprises SEQ ID NO: 14.

[0011] In another aspect, provided herein are conjugates comprising human TfR binding proteins described herein and a therapeutic agent. In some embodiments, the therapeutic agent is selected from a double stranded RNA (e.g., siRNA, saRNA), oligonucleotide (e.g., antisense oligonucleotide), polypeptide, small molecule, nanoparticle, lipid nanoparticle, exosome, antibody or antigen binding fragment thereof, or a combination thereof. In some embodiments, the therapeutic agent is a double stranded RNA (dsRNA). In some embodiments, the dsRNA comprises a sense strand and an antisense stand, wherein the antisense strand is complementaryto a target mRNA selected from SNCA, MAPT, APP, ATXN2, ATXN3, SARM1, APOE, BACE1, FMR1, LRRK2, HTT, SOD1, SCN10A, SCN9A or CACNA1B mRNA.

[0012] In some embodiments, the therapeutic agent is linked to the human TfR binding protein through a linker. In some embodiments, the linker is a Mal-Tet-TCO linker, SMCC linker, or GDM linker (structures of these linkers shown in Table 3).

[0013] In some embodiments, provided herein are conjugates of Formula (I): R-L-P, wherein R is a double stranded RNA (dsRNA) comprising a sense stand and an antisense strand; wherein L is a linker, or optionally absent, wherein P is a protein comprising one monovalent human TfR binding domain, wherein P comprises two heavy chains HC1 and HC2 and one light chain LC1, and wherein the HC1, HC2 and LC1 comprise the following sequences: (a) HC1 comprises SEQ ID NO: 11, LC1 comprises SEQ ID NO: 10, HC2 comprises SEQ ID NO: 12, or (b) HC1 comprises SEQ ID NO: 13, LC1 comprises SEQ ID NO: 10, HC2 comprises SEQ ID NO: 14.

[0014] In some embodiments, the dsRNA comprises an antisense strand complementary to a target mRNA selected from SNCA, MAPT, APP, ATXN2, ATXN3, SARM1, APOE, BACE1, FMR1, LRRK2, HTT, SOD1, SCN10A, SCN9A or CACNA1B mRNA. In some embodiments, the dsRNA comprises an antisense strand complementary to SNCA mRNA. In some embodiments, the dsRNA comprises an antisense strand complementary to MAPT mRNA.

[0015] Exemplary unmodified sense strand and antisense strand sequences of dsRNA targeting human SNCA mRNA are provided in Table 4a. In some embodiments, the sense strand and the antisense strand of the dsRNA comprise a pair of nucleic acid sequences selected from the group consisting of: (a) the sense strand comprises SEQ ID NO: 26, and the antisense strand comprises SEQ ID NO: 27; (b) the sense strand comprises SEQ ID NO: 28, and the antisense strand comprises SEQ ID NO: 29; (c) the sense strand comprises SEQ ID NO: 30, and the antisense strand comprises SEQ ID NO: 31; (d) the sense strand comprises SEQ ID NO: 32, and the antisense strand comprises SEQ ID NO: 33;(e) the sense strand comprises SEQ ID NO: 34, and the antisense strand comprises SEQ ID NO: 35; and (f) the sense strand comprises SEQ ID NO: 36, and the antisense strand comprises SEQ ID NO: 37; (g) the sense strand comprises SEQ ID NO: 38, and the antisense strand comprises SEQ ID NO: 27, wherein optionally one or more nucleotides of the sense strand and the antisense strand are independently modified nucleotides, and wherein optionally one or more internucleotide linkages of the sense strand and the antisense strand are modified internucleotide linkages. In some embodiments, the sense strand comprises SEQ ID NO: 26, and the antisense strand comprises SEQ ID NO: 27.

[0016] Exemplary unmodified sense strand and antisense strand sequences of dsRNA targeting human MAPT mRNA are provided in Table 4b. In some embodiments, the sense strand and the antisense strand of the dsRNA comprise a pair of nucleic acid sequences selected from the group consisting of: (a) the sense strand comprises SEQ ID NO: 39, and the antisense strand comprises SEQ ID NO: 40; (b) the sense strand comprises SEQ ID NO: 41, and the antisense strand comprises SEQ ID NO: 42; and (c) the sense strand comprises SEQ ID NO: 43, and the antisense strand comprises SEQ ID NO: 44, wherein optionally one or more nucleotides of the sense strand and the antisense strand are independently modified nucleotides, and wherein optionally one or more internucleotide linkages of the sense strand and the antisense strand are modified internucleotide linkages.

[0017] The dsRNA can include modifications. The modifications can be made to one or more nucleotides of the sense and / or antisense strand or to the internucleotide linkages. In some embodiments, one or more nucleotides of the sense strand and / or the antisense strand are independently modified nucleotides, which means the sense strand and the antisense strand can have different modified nucleotides. In some embodiments, each nucleotide of the sense strand is a modified nucleotide. In some embodiments, each nucleotide of the antisense strand is a modified nucleotide. In some embodiments, the modified nucleotide is a 2'-fluoro modifiednucleotide, 2'-O-methyl modified nucleotide, or 2'-O-alkyl (e.g., 2’-O-C16alkyl) modified nucleotide. In some embodiments, each nucleotide of the sense strand and the antisense strand is independently a modified nucleotide, e.g., a 2'-fluoro modified nucleotide, 2'-O-methyl modified nucleotide, or 2'-O-alkyl (e.g., 2’-O-C16alkyl) modified nucleotide.

[0018] In some embodiments, the sense strand has four 2'-fluoro modified nucleotides, e.g., at positions 7, 9, 10, 11 from the 5’ end of the sense strand. In some embodiments, the other nucleotides of the sense strand are 2'-O-methyl modified nucleotides. In some embodiments, the antisense strand has four 2'-fluoro modified nucleotides, e.g., at positions 2, 6, 14, 16 from the 5’ end of the antisense strand. In some embodiments, the other nucleotides of the antisense strand are 2'-O-methyl modified nucleotides.

[0019] In some embodiments, the sense strand has three 2'-fluoro modified nucleotides, e.g., at positions 9, 10, 11 from the 5’ end of the sense strand. In some embodiments, the other nucleotides of the sense strand are 2'-O-methyl modified nucleotides. In some embodiments, the antisense strand has five 2'-fluoro modified nucleotides, e.g., at positions 2, 5, 7, 14, 16 from the 5’ end of the antisense strand. In some embodiments, the antisense strand has five 2'-fluoro modified nucleotides, e.g., at positions 2, 5, 8, 14, 16 from the 5’ end of the antisense strand. In some embodiments, the antisense strand has five 2'-fluoro modified nucleotides, e.g., at positions 2, 3, 7, 14, 16 from the 5’ end of the antisense strand. In some embodiments, the other nucleotides of the antisense strand are 2'-O-methyl modified nucleotides.

[0020] In some embodiments, the 5’ end of the antisense strand has a phosphate analog, e.g., 5’-vinylphosphonate (5’-VP).

[0021] In some embodiments, the sense strand or the antisense strand comprises an abasic moiety or inverted abasic moiety.

[0022] In some embodiments, the sense strand and the antisense strand have one or more modified internucleotide linkages. In some embodiments, the modified internucleotide linkage is phosphorothioate linkage. In some embodiments, the sense strand has four or five phosphorothioate linkages. In some embodiments, the antisense strand has four or five phosphorothioate linkages. In some embodiments, the sense strand and the antisense strand each has four or five phosphorothioate linkages. In some embodiments, the sense strand has four phosphorothioate linkages and the antisense strand has five phosphorothioate linkages.

[0023] Exemplary modified sense strand and antisense strand sequences of dsRNA targeting human SNCA mRNA are provided in Table 6a. Exemplary modified sense strand and antisense strand sequences of dsRNA targeting human MAPT mRNA are provided in Table 6b.

[0024] In another aspect, provided herein are methods of treating a CNS disease, e.g., a neurodegenerative disease, in a patient in need thereof, and such the method comprises administering to the patient an effective amount of the human TfR binding protein or conjugate or a pharmaceutical composition described herein.

[0025] In a further aspect, provided herein are methods of treating a neurodegenerative synucleinopathy in a patient in need thereof, and such the method comprises administering to the patient an effective amount of the human TfR binding proteins or conjugate or a pharmaceutical composition described herein (e.g., a TBP-SNCA siRNA conjugate described herein or a pharmaceutical composition comprising such a TBP-SNCA siRNA conjugate). In some embodiments, the neurodegenerative synucleinopathy is selected from Parkinson’s disease, Alzheimer’s disease, multiple system atrophy, or Lewy body dementia. The human TfR binding protein or conjugate or a pharmaceutical composition can be administered to the patient intravenously or subcutaneously.

[0026] In a further aspect, provided herein are methods of treating a tauopathy in a patient in need thereof, and such the method comprises administering to the patient an effective amount of the human TfR binding proteins or conjugate or a pharmaceutical composition described herein (e.g., a TBP-MAPT siRNA conjugate described herein or a pharmaceutical composition comprising such a TBP-MAPT siRNA conjugate). In some embodiments, the tauopathy is selected from Alzheimer’s disease, frontotemporal dementia (FTD), frontotemporal dementia with parkinsonism linked to chromosome 17 (FTDP-17), frontotemporal lobar degeneration (FTLD), behavioral variant frontotemporal dementia (bvFTD), nonfluent variant primary progressive aphasia (nfvPPA), Parkinson’s discase, Pick’s disease (PiD), primary progressive aphasia - semantic (PPA-S), primary progressive aphasia - logopenic (PPA-L), multiple system tauopathy with presenile dementia (MSTD), neurofibrillary tangle (NFT) dementia, FTD with motor neuron disease, progressive supranuclear palsy (PSP), amyotrophic lateral sclerosis / parkinsonism-dementia complex (ALS-PDC), argyrophilic grain dementia (AGD), British type amyloid angiopathy, cerebral amyloid angiopathy, chronic traumatic encephalopathy (CTE), corticobasal degeneration (CBD), Creutzfeldt-Jakob disease (CJD),dementia pugilistica, diffuse neurofibrillary tangles with calcification, Down’s syndrome, epilepsy, Gerstmann-Straussler-Scheinker disease, Hallervorden-Spatz disease, Huntington’s disease, inclusion body myositis, lead encephalopathy, Lytico-Bodig disease, meningioangiomatosis, multiple system atrophy, myotonic dystrophy, Niemann-Pick disease type C (NP-C), non-Guamanian motor neuron disease with neurofibrillary tangles, postencephalitic parkinsonism, prion protein cerebral amyloid angiopathy, progressive subcortical gliosis, tangle only dementia, tangle-predominant dementia, ganglioglioma, gangliocytoma, subacute sclerosingpan encephalitis, tuberous sclerosis, lipofuscinosis, primary age-related tauopathy (PART), or globular glial tauopathies (GGT). The human TfR binding protein or conjugate or a pharmaceutical composition can be administered to the patient intravenously or subcutaneously.

[0027] In another aspect, provided herein are human TfR binding proteins or conjugates described herein or pharmaceutical compositions comprising such human TfR binding proteins or conjugates for use in a therapy. Also provided herein are human TfR binding proteins or conjugates described herein or pharmaceutical compositions comprising such human TfR binding proteins or conjugates (e.g., a TBP-SNCA siRNA conjugate described herein or a pharmaceutical composition comprising such a TBP-SNCA siRNA conjugate) for use in the treatment of a neurodegenerative synucleinopathy, e.g., Parkinson’s disease, Alzheimer’s disease, multiple system atrophy, or Lewy body dementia. Also provided herein are human TfR binding proteins or conjugates described herein or pharmaceutical compositions comprising such human TfR binding proteins or conjugates (e.g., a TBP-MAPT siRNA conjugate described herein or a pharmaceutical composition comprising such a TBP-MAPT siRNA conjugate) for use in the treatment of a tauopathy, e.g., e.g., Alzheimer’s disease, frontotemporal dementia (FTD), frontotemporal dementia with parkinsonism linked to chromosome 17 (FTDP-17), frontotemporal lobar degeneration (FTLD), behavioral variant frontotemporal dementia (bvFTD), nonfluent variant primary progressive aphasia (nfvPPA), Parkinson’s discase, Pick’s disease (PiD), primary progressive aphasia - semantic (PPA-S), primary progressive aphasia - logopenic (PPA-L), multiple system tauopathy with presenile dementia (MSTD), neurofibrillary tangle (NFT) dementia, FTD with motor neuron disease, progressive supranuclear palsy (PSP), amyotrophic lateral sclerosis / parkinsonism-dementia complex (ALS-PDC), argyrophilic grain dementia (AGD), British type amyloid angiopathy, cerebral amyloid angiopathy, chronictraumatic encephalopathy (CTE), corticobasal degeneration (CBD), Creutzfeldt-Jakob disease (CJD), dementia pugilistica, diffuse neurofibrillary tangles with calcification, Down’s syndrome, epilepsy, Gerstmann-Straussler-Scheinker disease, Hallervorden-Spatz disease, Huntington’s disease, inclusion body myositis, lead encephalopathy, Lytico-Bodig disease, meningioangiomatosis, multiple system atrophy, myotonic dystrophy, Niemann-Pick disease type C (NP-C), non-Guamanian motor neuron disease with neurofibrillary tangles, postencephalitic parkinsonism, prion protein cerebral amyloid angiopathy, progressive subcortical gliosis, tangle only dementia, tangle-predominant dementia, ganglioglioma, gangliocytoma, subacute sclerosingpan encephalitis, tuberous sclerosis, lipofuscinosis, primary age-related tauopathy (PART), or globular glial tauopathies (GGT).

[0028] In another aspect, provided herein are uses of human TfR binding proteins or conjugates described herein in the manufacture of a medicament for treating a CNS disease, e.g., a neurodegenerative disease. In some embodiments, the neurodegenerative disease is a neurodegenerative synucleinopathy, e.g., Parkinson’s disease, Alzheimer’s disease, multiple system atrophy, or Lewy body dementia. In some embodiments, the neurodegenerative disease is a tauopathy, e.g., Alzheimer’s disease, frontotemporal dementia (FTD), frontotemporal dementia with parkinsonism linked to chromosome 17 (FTDP-17), frontotemporal lobar degeneration (FTLD), behavioral variant frontotemporal dementia (bvFTD), nonfluent variant primary progressive aphasia (nfvPPA), Parkinson’s discase, Pick’s disease (PiD), primary progressive aphasia - semantic (PPA-S), primary progressive aphasia - logopenic (PPA-L), multiple system tauopathy with presenile dementia (MSTD), neurofibrillary tangle (NFT) dementia, FTD with motor neuron disease, progressive supranuclear palsy (PSP), amyotrophic lateral sclerosis / parkinsonism-dementia complex (ALS-PDC), argyrophilic grain dementia (AGD), British type amyloid angiopathy, cerebral amyloid angiopathy, chronic traumatic encephalopathy (CTE), corticobasal degeneration (CBD), Creutzfeldt-Jakob disease (CJD), dementia pugilistica, diffuse neurofibrillary tangles with calcification, Down’s syndrome, epilepsy, Gerstmann- Straussler-Scheinker disease, Hallervorden-Spatz disease, Huntington’s disease, inclusion body myositis, lead encephalopathy, Lytico-Bodig disease, meningioangiomatosis, multiple system atrophy, myotonic dystrophy, Niemann-Pick disease type C (NP-C), non-Guamanian motor neuron disease with neurofibrillary tangles, postencephalitic parkinsonism, prion protein cerebral amyloid angiopathy, progressive subcortical gliosis, tangle only dementia, tangle-predominantdementia, ganglioglioma, gangliocytoma, subacute sclerosingpan encephalitis, tuberous sclerosis, lipofuscinosis, primary age-related tauopathy (PART), or globular glial tauopathies (GGT). BRIEF DESCRIPTION OF THE DRAWINGS

[0029] Figure 1A shows an exemplary analytical anion exchange (AEX) chromatogram of DAR profile for TBP3-SMCC-dsRNA No. 26 conjugate after purification. Figure 1B shows an exemplary AEX chromatogram of DAR profile for TBP3-SMCC-dsRNA No. 13 conjugate after purification. Figure 1C shows an exemplary AEX chromatogram of DAR profile for TBP2-SMCC-dsRNA No. 26 conjugate after purification. Figure 1D shows an exemplary AEX chromatogram of DAR profile for TBP2-SMCC-dsRNA No.13 conjugate after purification. Figure 1E shows an exemplary AEX chromatogram of DAR profile for mTBP2-SMCC-dsRNA No. 26 conjugate after purification.

[0030] Figure 2A shows MAPT mRNA reduction in Cynomolgus monkey tissues 29 days after a single intravenous (IV) delivery of TBP2-SMCC-dsRNA No.26 conjugate at 20 mg / kg siRNA dose. Figure 2B shows MAPT mRNA reduction in Cynomolgus monkey tissues 29 days after a single IV delivery of TBP3-SMCC-dsRNA No. 26 conjugate at 20 mg / kg siRNA dose. The error bars in Figures 2A and 2B are Standard Error of the Mean and statistical analysis was performed with a one-way ANOVA with Dunnett’s multiple comparison test against PBS control group. Annotations indicate P values >0.0001 to 0.05=*.

[0031] Figure 3 show SNCA mRNA reduction in mouse brain 28 days following a single IV delivery of TBP2-SMCC-dsRNA No. 13 or TBP3-SMCC-dsRNA No. 13 conjugate at 0.1, 0.5 or 5 mg / kg siRNA dose. The error bars in Figure 3 are Standard Deviations and statistical analysis was performed with a one-way ANOVA with Dunnett’s multiple comparison test against PBS control group. Annotations indicate P values >0.0001=****; >0.001=***; >0.01=**; >0.05=*.

[0032] Figure 4 show MAPT mRNA reduction in human tau transgenic mouse brain 28 days following a single IV delivery of mTBP2-SMCC-dsRNA No. 26 conjugate at 1, 10 or 100 mg / kg siRNA dose. The error bars in Figure 4 are Standard Deviations and statistical analysis was performed with a one-way ANOVA with Dunnett’s multiple comparison test against PBS control group. Annotations indicate P values >0.0001=****; >0.001=***; >0.01=**; >0.05=*.DETAILED DESCRIPTION

[0033] Provided herein are proteins comprising one monovalent human TfR binding domain (“human TfR binding proteins”), conjugates comprising such human TfR binding proteins, e.g., human TfR binding proteins-dsRNA conjugates, pharmaceutical compositions comprising human TfR binding proteins or conjugates, and methods of treating CNS diseases (e.g., neurodegenerative disease such as neurodegenerative synucleinopathy or tauopathy) using human TfR binding proteins or conjugates. The conjugates comprising human TfR binding proteins provided herein have improved yield and / or reduced microheterogeneity. Human TfR binding proteins

[0034] In one aspect, provided herein are proteins comprising one monovalent human TfR binding domain (“human TfR binding proteins”). In some embodiments, the monovalent human TfR binding domain comprises a heavy chain variable region (VH) and a light chain variable region (VL), and the VH comprises heavy chain complementarity determining regions HCDR1, HCDR2, and HCDR3, and the VL comprises light chain complementarity determining regions LCDR1, LCDR2, and LCDR3. In some embodiments, the monovalent human TfR binding domain comprises a VH comprising HCDR1, HCDR2, and HCDR3 selected from Table 1a. In some embodiments, the monovalent human TfR binding domain comprises a VL comprising LCDR1, LCDR2, and LCDR3 selected from Table 1a. In some embodiments, the monovalent human TfR binding domain comprises a VH comprising HCDR1, HCDR2, and HCDR3 selected from Table 1a, and / or a VL comprising LCDR1, LCDR2, and LCDR3 selected from Table 1a. In some embodiments, the monovalent human TfR binding domain comprises a VH and / or a VL selected from Table 1a. In some embodiments, the human TfR binding proteins described herein also bind cynomolgus monkey TfR. Table 1a. Sequences of human TfR binding domains and proteins Region Sequence SEQ ID NOLCDR1 RASQGISHYLV 4 (KABAT) LCDR2 AASSLQS 5OAH2 HC1 EVQLVESGGGLVKPGGSLRLSCVASGFTFSSYSMNW 13 (IgG4PAA) VRQAPGKGLEWVSSISSSSSYIYYADSVKGRFTISRD NAKNSLYLQMNSLRAEDTAVYYCARRHGYSNSDAFTable 1b. Sequences of human TfR binding proteins Human TfR binding HC1 LC1 HC2 protein (TBP)

[0035] In some embodiments, the monovalent human TfR binding domain comprises a heavy chain variable region (VH) and a light chain variable region (VL), and the VH comprises heavy chain complementarity determining regions HCDR1, HCDR2, and HCDR3, and the VL comprises light chain complementarity determining regions LCDR1, LCDR2, and LCDR3. In some embodiments, HCDR1 comprises SEQ ID NO: 1, HCDR2 comprises SEQ ID NO: 2, HCDR3 comprises SEQ ID NO: 3, LCDR1 comprises SEQ ID NO: 4, LCDR2 comprises SEQ ID NO: 5, and LCDR3 comprises SEQ ID NO: 6. In some embodiments, VH comprises SEQ ID NO: 7, and VL comprises SEQ ID NO: 8. In some embodiments, VH comprises a sequencehaving at least 95% sequence identity to SEQ ID NO: 7, and VL comprises a sequence having at least 95% sequence identity to SEQ ID NO: 8.

[0036] In some embodiments, the monovalent human TfR binding domain is an antibody fragment, e.g., Fab, scFv, Fv, or scFab (single chain Fab). In some embodiments, the monovalent human TfR binding domain is Fab. In some embodiments, the human TfR binding domain further comprises a heavy chain constant region and / or a light chain constant region.

[0037] In some embodiments, the human TfR binding protein further comprises a half- life extender, e.g., an immunoglobulin Fc region or a VHH that binds human serum albumin (HSA).

[0038] In some embodiments, the human TfR binding protein further comprises an immunoglobulin Fc region, e.g., a modified human IgG4 Fc region, or a modified human IgG1 Fc region. In some embodiments, the human TfR binding protein further comprises a modified human IgG4 Fc region comprising proline at residue 228, and alanine at residues 234 and 235 (all residues are numbered according to the EU Index numbering, also called hIgG4PAA Fc region). In some embodiments, the human TfR binding protein further comprises a modified human IgG1 Fc region comprising alanine at residues 234, 235, and 329, serine at position 265, aspartic acid at position 436 (all residues are numbered according to the EU Index numbering, also called hIgG1 effector null or hIgG1EN Fc region).

[0039] In some embodiments, the human TfR binding protein comprises heterodimeric mutations. In some embodiments, the human TfR binding protein comprises a modified Fc region comprising a first Fc CH3 domain comprising serine at residue 349, methionine at residue 366, tyrosine at residue 370, and valine at residue 409, and a second Fc CH3 domain comprising glycine at residue 356, aspartic acid at residue 357, glutamine at residue 364 and alanine at residue 407 (all residues are numbered according to the EU Index numbering). In some embodiments, the human TfR binding protein comprises a modified Fc region comprising a first Fc CH3 domain comprising leucine at residue 405, and a second Fc CH3 domain comprising arginine at residue 409 (all residues are numbered according to the EU Index numbering).

[0040] In some embodiments, the human TfR binding protein comprises one or more native cysteine residues, which can be used for conjugation. For example, in some embodiments, the human TfR binding protein comprises a native cysteine at position 220 of the light chainand / or a native cysteine at position 226 of the heavy chain, which can be used for conjugation (all residues according to the EU Index numbering).

[0041] In some embodiments, the human TfR binding protein comprises engineered cysteine residues for conjugation. The approach of including engineered cysteines as a means for conjugation has been described in WO 2018 / 232088. In some embodiments, the human TfR binding protein comprises a heavy chain comprising one or more cysteines at the following residues: 124, 157, 162, 262, 373, 375, 378, 397, 415 (all residues according to the EU Index numbering). In some embodiments, the human TfR binding protein comprises a light chain (e.g., a kappa light chain) comprising one or more cysteines at the following residues: 156, 171, 191, 193, 202, 208 (all residues according to the EU Index numbering). In some embodiments, the human TfR binding protein comprises a heavy chain constant region comprising cysteine at residue 124 (according to the EU Index numbering). In some embodiments, the human TfR binding protein comprises a light chain constant region comprising cysteine at residue 156 (according to the EU Index numbering). In some embodiments, the human TfR binding protein comprises an immunoglobulin Fc region comprising cysteine at residue 378 (according to the EU Index numbering).

[0042] In some embodiments, the human TfR binding protein is any one of the human TfR binding proteins in Table 1b.

[0043] In some embodiments, provided herein are proteins comprising one monovalent human transferrin receptor (TfR) binding domain, wherein the protein comprises two heavy chains HC1 and HC2 and one light chain LC1, and wherein the HC1, HC2 and LC1 comprise the following sequences: (c) HC1 comprises SEQ ID NO: 11, LC1 comprises SEQ ID NO: 10, HC2 comprises SEQ ID NO: 12, or (d) HC1 comprises SEQ ID NO: 13, LC1 comprises SEQ ID NO: 10, HC2 comprises SEQ ID NO: 14.

[0044] In some embodiments, the human TfR binding protein has a one arm heteromab format. In some embodiments, the human TfR binding protein comprises two heavy chains HC1 and HC2 and one light chain LC1, wherein HC1 comprises SEQ ID NO: 11, LC1 comprises SEQ ID NO: 10, HC2 comprises SEQ ID NO: 12. In some embodiments, provided herein are human TfR binding proteins comprise two heavy chains HC1 and HC2 and one light chain LC1,wherein HC1 comprises SEQ ID NO: 13, LC1 comprises SEQ ID NO: 10, HC2 comprises SEQ ID NO: 14.

[0045] The human TfR binding proteins described herein can be recombinantly produced in a host cell, for example, using an expression vector. For example, an expression vector may include a sequence that encodes one or more signal peptides that facilitate secretion of the polypeptide(s) from a host cell. Expression vectors containing a polynucleotide of interest (e.g., a polynucleotide encoding a heavy chain or light chain of the TfR binding proteins) may be transferred into a host cell by well-known methods. Additionally, expression vectors may contain one or more selection markers, e.g., tetracycline, neomycin, and dihydrofolate reductase, to aide in detection of host cells transformed with the desired polynucleotide sequences.

[0046] A host cell includes cells stably or transiently transfected, transformed, transduced or infected with one or more expression vectors expressing all or a portion of the TfR binding proteins described herein. According to some embodiments, a host cell may be stably or transiently transfected, transformed, transduced or infected with an expression vector expressing HC polypeptides and an expression vector expressing LC polypeptides of the TfR binding proteins described herein. In some embodiments, a host cell may be stably or transiently transfected, transformed, transduced or infected with an expression vector expressing HC and LC polypeptides of the TfR binding proteins described herein. The TfR binding proteins may be produced in mammalian cells such as CHO, NS0, HEK293 or COS cells according to techniques well known in the art.

[0047] Medium, into which the TfR binding proteins has been secreted, may be purified by conventional techniques, such as mixed-mode methods of ion-exchange and hydrophobic interaction chromatography. For example, the medium may be applied to and eluted from a Protein A or G column using conventional methods; mixed-mode methods of ion-exchange and hydrophobic interaction chromatography may also be used. Soluble aggregate and multimers may be effectively removed by common techniques, including size exclusion, hydrophobic interaction, ion exchange, or hydroxyapatite chromatography. Various methods of protein purification may be employed, and such methods are known in the art and described, for example, in Deutscher, Methods in Enzymology 182: 83-89 (1990) and Scopes, Protein Purification: Principles and Practice, 3rd Edition, Springer, NY (1994). Mouse TfR binding proteins

[0048] Some conjugates used in the Examples below comprise a protein comprising one monovalent mouse TfR binding domain (“mouse TfR binding proteins” or mTBP). Exemplary sequences of mouse TfR binding proteins are provided in Tables 2A and 2B. Such conjugates comprising a mouse TfR binding protein can serve as surrogate molecules in mouse models. Table 2A. Exemplary sequences of mouse TfR binding proteins Region Sequence SEQ ID NO HCDR1 GSYWIC 15HC2 ESKYGPPCPPCPAPEAAGGPSVFLFPPKPKDTLM 25 ISRTPEVTCVVVDVSQEDPEVQFNWYVDGVEV HNAKTKPREEQFNSTYRVVSVLTVLHQDWLNGTable 2B. Exemplary sequences of mouse TfR binding proteins Mouse TfR binding HC1 LC1 HC2 protein (mTBP)Conjugates comprising human TfR binding protein

[0049] In another aspect, provided herein are conjugates comprising human TfR binding proteins or antibodies described herein and a therapeutic agent. In some embodiments, the therapeutic agent is selected from a double stranded RNA (e.g., siRNA, saRNA), oligonucleotide (e.g., antisense oligonucleotide), polypeptide, small molecule, nanoparticle, lipid nanoparticle, exosome, antibody or antigen binding fragment thereof, or a combination thereof. In some embodiments, the therapeutic agent is a double stranded RNA (dsRNA). In some embodiments, the dsRNA comprises a sense strand and an antisense stand, wherein the antisense strand is complementary to a target mRNA selected from SNCA, MAPT, APP, ATXN2, ATXN3, SARM1, APOE, BACE1, FMR1, LRRK2, HTT, SOD1, SCN10A, SCN9A or CACNA1BmRNA. In some embodiments, the dsRNA comprises a sense strand and an antisense stand, wherein the antisense strand is complementary to SNCA mRNA. In some embodiments, the dsRNA comprises a sense strand and an antisense stand, wherein the antisense strand is complementary to MAPT mRNA.

[0050] In some embodiments, the human TfR binding proteins described herein comprise one or more native cysteine residues, which can be used for conjugation. For example, in some embodiments, the human TfR binding protein described herein comprises a native cysteine at position 220 of the light chain and / or a native cysteine at position 226 of the heavy chain, which can be used for conjugation (all residues according to the EU Index numbering).

[0051] In some embodiments, the human TfR binding proteins described herein comprise one or more engineered cysteine residues for conjugation. The approach of including engineered cysteines as a means for conjugation has been described in WO 2018 / 232088. In some embodiments, the human TfR binding proteins described herein comprise a heavy chain comprising one or more cysteines at the following residues: 124, 157, 162, 262, 373, 375, 378, 397, 415 (all residues according to the EU Index numbering). In some embodiments, the human TfR binding proteins described herein comprise a light chain (e.g., a kappa light chain) comprising one or more cysteines at the following residues: 156, 171, 191, 193, 202, 208 (all residues according to the EU Index numbering). In some embodiments, the human TfR binding proteins described herein comprise a heavy chain constant region comprising cysteine at residue 124 (according to the EU Index numbering). In some embodiments, the human TfR binding proteins described herein comprise a light chain constant region comprising cysteine at residue 156 (according to the EU Index numbering). In some embodiments, the human TfR binding proteins described herein comprise an immunoglobulin Fc region comprising cysteine at residue 378 (according to the EU Index numbering).

[0052] In some embodiments, the therapeutic agent is linked to the human TfR binding protein through a linker. In some embodiments, the linker is a Mal-Tet-TCO linker, SMCC linker, or GDM linker (structures of these linkers shown in Table 3).Table 3. Exemplary linker structures Linker Structure10Hydrolyzed ring open form of SMCC linker 2

[0053] In some embodiments, provided herein are conjugates of Formula (I): R-L-P, wherein R is a double stranded RNA (dsRNA) comprising a sense stand and an antisense strand; wherein L is a linker, or optionally absent, wherein P is a protein comprising one monovalent human TfR binding domain, wherein P comprises two heavy chains HC1 and HC2 and one light chain LC1, and wherein the HC1, HC2 and LC1 comprise the following sequences: (a) HC1 comprises SEQ ID NO: 11, LC1 comprises SEQ ID NO: 10, HC2 comprises SEQ ID NO: 12, or (b) HC1 comprises SEQ ID NO: 13, LC1 comprises SEQ ID NO: 10, HC2 comprises SEQ ID NO: 14.

[0054] In some embodiments, P comprises two heavy chains HC1 and HC2 and one light chain LC1, wherein HC1 comprises SEQ ID NO: 11, LC1 comprises SEQ ID NO: 10, HC2 comprises SEQ ID NO: 12.

[0055] In some embodiments, P comprises two heavy chains HC1 and HC2 and one light chain LC1, wherein HC1 comprises SEQ ID NO: 13, LC1 comprises SEQ ID NO: 10, HC2 comprises SEQ ID NO: 14.

[0056] In some embodiments, L is present and selected from: a Mal-Tet-TCO linker, SMCC linker, or GDM linker (see Table 3). In some embodiments, L is a SMCC linker. In some embodiments, L is absent.

[0057] In some embodiments, P is linked to the 3’ end of the sense strand of the dsRNA. In some embodiments, P is linked to the 5’ end of the sense strand of the dsRNA. In some embodiments, P is linked to an internal position of the sense strand of the dsRNA. In some embodiments, P is linked to the 3’ end of the antisense strand of the dsRNA. In some embodiments, P is linked to an internal position of the antisense strand of the dsRNA.

[0058] The conjugates described herein can be made by a variety of procedures known to one of ordinary skill in the art, some of which are illustrated in the preparations and examplesbelow, e.g., in Example 3. One of ordinary skill in the art recognizes that the specific synthetic steps for each of the routes described may be combined in different ways, or in conjunction with steps from different schemes, to prepare conjugates. The product of each step can be recovered by conventional methods well known in the art, including extraction, evaporation, precipitation, chromatography, filtration, trituration, and crystallization. The reagents and starting materials are readily available to one of ordinary skill in the art.

[0059] In some embodiments, the TfR binding proteins with native or engineered cysteines described herein can be first treated with a reducing agent, e.g., DTT, and then re- oxidized with an oxidizing agent, e.g., DHAA. The resulting oxidized TfR binding proteins are then incubated with a linker functionalized therapeutic agent, e.g., linker-dsRNA, to produce the conjugates.

[0060] In some embodiments, the dsRNA comprises an antisense strand complementary to a target mRNA selected from SNCA, MAPT, APP, ATXN2, ATXN3, SARM1, APOE, BACE1, FMR1, LRRK2, HTT, SOD1, SCN10A, SCN9A or CACNA1B mRNA. In some embodiments, the dsRNA comprises an antisense strand complementary to SNCA mRNA. In some embodiments, the dsRNA comprises an antisense strand complementary to MAPT mRNA.

[0061] In some embodiments, the sense strand and the antisense strand of the dsRNA are each 15-30 nucleotides in length, e.g., 20-25 nucleotides in length. In some embodiments, the dsRNA has a sense strand of 21 nucleotides and an antisense strand of 23 nucleotides. In some embodiments, the sense strand and antisense strand of the dsRNA may have overhangs at either the 5’ end or the 3’ end (i.e., 5’ overhang or 3’ overhang). For example, the sense strand and the antisense strand may have 5’ or 3’ overhangs of 1 to 5 nucleotides or 1 to 3 nucleotides. In some embodiments, the antisense strand comprises a 3’ overhang of two nucleotides.

[0062] Exemplary unmodified sense strand and antisense strand sequences of dsRNA targeting human SNCA mRNA are provided in Table 4a. Exemplary unmodified sense strand and antisense strand sequences of dsRNA targeting human MAPT mRNA are provided in Table 4b.Table 4a. Unmodified Nucleic Acid Sequences of dsRNA targeting human SNCA mRNA (SNCA siRNA) dsRNA Sense Strand (5' to 3') SEQ Antisense Strand (5' to 3') SEQ Start No. ID ID position NO NO of target n pt 03Table 4b. Unmodified Nucleic Acid Sequences of dsRNA targeting human MAPT mRNA (MAPT siRNA) dsRNA Sense Strand (5' to 3') SEQ Antisense Strand (5' to 3') SEQ Start No. ID ID position t n pt 11

[0063] In some embodiments, the dsRNA targets SNCA mRNA. In some embodiments, the sense strand and the antisense strand of the dsRNA comprise a pair of nucleic acid sequences selected from the group consisting of: (a) the sense strand comprises a first nucleic acid sequence having at least 90% sequence identity to SEQ ID NO: 26, and the antisense strand comprises a second nucleic acid sequence having at least 90% sequence identity to SEQ ID NO: 27;(b) the sense strand comprises a first nucleic acid sequence having at least 90% sequence identity to SEQ ID NO: 28, and the antisense strand comprises a second nucleic acid sequence having at least 90% sequence identity to SEQ ID NO: 29; (c) the sense strand comprises a first nucleic acid sequence having at least 90% sequence identity to SEQ ID NO: 30, and the antisense strand comprises a second nucleic acid sequence having at least 90% sequence identity to SEQ ID NO: 31; (d) the sense strand comprises a first nucleic acid sequence having at least 90% sequence identity to SEQ ID NO: 32, and the antisense strand comprises a second nucleic acid sequence having at least 90% sequence identity to SEQ ID NO: 33; (e) the sense strand comprises a first nucleic acid sequence having at least 90% sequence identity to SEQ ID NO: 34, and the antisense strand comprises a second nucleic acid sequence having at least 90% sequence identity to SEQ ID NO: 35; (f) the sense strand comprises a first nucleic acid sequence having at least 90% sequence identity to SEQ ID NO: 36, and the antisense strand comprises a second nucleic acid sequence having at least 90% sequence identity to SEQ ID NO: 37; and (g) the sense strand comprises a first nucleic acid sequence having at least 90% sequence identity to SEQ ID NO: 38, and the antisense strand comprises a second nucleic acid sequence having at least 90% sequence identity to SEQ ID NO: 27, wherein optionally one or more nucleotides of the sense strand and the antisense strand are independently modified nucleotides, and wherein optionally one or more internucleotide linkages of the sense strand and the antisense strand are modified internucleotide linkages.

[0064] In some embodiments, the sense strand and the antisense strand of the dsRNA comprise a pair of nucleic acid sequences selected from the group consisting of: (a) the sense strand comprises a first nucleic acid sequence having at least 95% sequence identity to SEQ ID NO: 26, and the antisense strand comprises a second nucleic acid sequence having at least 95% sequence identity to SEQ ID NO: 27; (b) the sense strand comprises a first nucleic acid sequence having at least 95% sequence identity to SEQ ID NO: 28, and the antisense strand comprises a second nucleic acid sequence having at least 95% sequence identity to SEQ ID NO: 29;(c) the sense strand comprises a first nucleic acid sequence having at least 95% sequence identity to SEQ ID NO: 30, and the antisense strand comprises a second nucleic acid sequence having at least 95% sequence identity to SEQ ID NO: 31; (d) the sense strand comprises a first nucleic acid sequence having at least 95% sequence identity to SEQ ID NO: 32, and the antisense strand comprises a second nucleic acid sequence having at least 95% sequence identity to SEQ ID NO: 33; (e) the sense strand comprises a first nucleic acid sequence having at least 95% sequence identity to SEQ ID NO: 34, and the antisense strand comprises a second nucleic acid sequence having at least 95% sequence identity to SEQ ID NO: 35; (f) the sense strand comprises a first nucleic acid sequence having at least 95% sequence identity to SEQ ID NO: 36, and the antisense strand comprises a second nucleic acid sequence having at least 95% sequence identity to SEQ ID NO: 37; and (g) the sense strand comprises a first nucleic acid sequence having at least 95% sequence identity to SEQ ID NO: 38, and the antisense strand comprises a second nucleic acid sequence having at least 95% sequence identity to SEQ ID NO: 27, wherein optionally one or more nucleotides of the sense strand and the antisense strand are independently modified nucleotides, and wherein optionally one or more internucleotide linkages of the sense strand and the antisense strand are modified internucleotide linkages.

[0065] In some embodiments, the sense strand and the antisense strand of the dsRNA comprise a pair of nucleic acid sequences selected from the group consisting of: (a) the sense strand comprises SEQ ID NO: 26, and the antisense strand comprises SEQ ID NO: 27; (b) the sense strand comprises SEQ ID NO: 28, and the antisense strand comprises SEQ ID NO: 29; (c) the sense strand comprises SEQ ID NO: 30, and the antisense strand comprises SEQ ID NO: 31; (d) the sense strand comprises SEQ ID NO: 32, and the antisense strand comprises SEQ ID NO: 33; (e) the sense strand comprises SEQ ID NO: 34, and the antisense strand comprises SEQ ID NO: 35;(f) the sense strand comprises SEQ ID NO: 36, and the antisense strand comprises SEQ ID NO: 37; and (g) the sense strand comprises SEQ ID NO: 38, and the antisense strand comprises SEQ ID NO: 27, wherein optionally one or more nucleotides of the sense strand and the antisense strand are independently modified nucleotides, and wherein optionally one or more internucleotide linkages of the sense strand and the antisense strand are modified internucleotide linkages.

[0066] In some embodiments, the dsRNA targets MAPT mRNA. In some embodiments, the sense strand and the antisense strand of the dsRNA comprise a pair of nucleic acid sequences selected from the group consisting of: (a) the sense strand comprises a first nucleic acid sequence having at least 90% sequence identity to SEQ ID NO: 39, and the antisense strand comprises a second nucleic acid sequence having at least 90% sequence identity to SEQ ID NO: 40; (b) the sense strand comprises a first nucleic acid sequence having at least 90% sequence identity to SEQ ID NO: 41, and the antisense strand comprises a second nucleic acid sequence having at least 90% sequence identity to SEQ ID NO: 42; and (c) the sense strand comprises a first nucleic acid sequence having at least 90% sequence identity to SEQ ID NO: 43, and the antisense strand comprises a second nucleic acid sequence having at least 90% sequence identity to SEQ ID NO: 44, wherein optionally one or more nucleotides of the sense strand and the antisense strand are independently modified nucleotides, and wherein optionally one or more internucleotide linkages of the sense strand and the antisense strand are modified internucleotide linkages.

[0067] In some embodiments, the sense strand and the antisense strand of the dsRNA comprise a pair of nucleic acid sequences selected from the group consisting of: (a) the sense strand comprises a first nucleic acid sequence having at least 95% sequence identity to SEQ ID NO: 39, and the antisense strand comprises a second nucleic acid sequence having at least 95% sequence identity to SEQ ID NO: 40; (b) the sense strand comprises a first nucleic acid sequence having at least 95% sequence identity to SEQ ID NO: 41, and the antisense strand comprises a second nucleic acid sequence having at least 95% sequence identity to SEQ ID NO: 42; and(c) the sense strand comprises a first nucleic acid sequence having at least 95% sequence identity to SEQ ID NO: 43, and the antisense strand comprises a second nucleic acid sequence having at least 95% sequence identity to SEQ ID NO: 44, wherein optionally one or more nucleotides of the sense strand and the antisense strand are independently modified nucleotides, and wherein optionally one or more internucleotide linkages of the sense strand and the antisense strand are modified internucleotide linkages.

[0068] In some embodiments, the sense strand and the antisense strand of the dsRNA comprise a pair of nucleic acid sequences selected from the group consisting of: (a) the sense strand comprises SEQ ID NO: 39, and the antisense strand comprises SEQ ID NO: 40; (b) the sense strand comprises SEQ ID NO: 41, and the antisense strand comprises SEQ ID NO: 42; and (c) the sense strand comprises SEQ ID NO: 43, and the antisense strand comprises SEQ ID NO: 44, wherein optionally one or more nucleotides of the sense strand and the antisense strand are independently modified nucleotides, and wherein optionally one or more internucleotide linkages of the sense strand and the antisense strand are modified internucleotide linkages.

[0069] The dsRNA can include modifications. The modifications can be made to one or more nucleotides of the sense and / or antisense strand or to the internucleotide linkages, which are the bonds between two nucleotides in the sense or antisense strand. For example, some 2’- modifications of ribose or deoxyribose can increase RNA or DNA stability and half-life. Such 2’-modifications can be 2’-fluoro, 2’-O-methyl (i.e., 2’-methoxy), or 2'-O-alkyl (e.g., 2’-O-C16 alkyl).

[0070] In some embodiments, one or more nucleotides of the sense strand and / or the antisense strand are independently modified nucleotides, which means the sense strand and the antisense strand can have different modified nucleotides. In some embodiments, each nucleotide of the sense strand is a modified nucleotide. In some embodiments, each nucleotide of the antisense strand is a modified nucleotide. In some embodiments, the modified nucleotide is a 2'- fluoro modified nucleotide, 2'-O-methyl modified nucleotide, or 2'-O-alkyl (e.g., 2’-O-C16 alkyl) modified nucleotide. In some embodiments, each nucleotide of the sense strand and the antisensestrand is independently a modified nucleotide, e.g., a 2'-fluoro modified nucleotide, 2'-O-methyl modified nucleotide, or 2'-O-alkyl (e.g., 2’-O-C16 alkyl) modified nucleotide.

[0071] In some embodiments, the sense strand has four 2'-fluoro modified nucleotides, e.g., at positions 7, 9, 10, 11 from the 5’ end of the sense strand. In some embodiments, the other nucleotides of the sense strand are 2'-O-methyl modified nucleotides. In some embodiments, the antisense strand has four 2'-fluoro modified nucleotides, e.g., at positions 2, 6, 14, 16 from the 5’ end of the antisense strand. In some embodiments, the other nucleotides of the antisense strand are 2'-O-methyl modified nucleotides.

[0072] In some embodiments, the sense strand has three 2'-fluoro modified nucleotides, e.g., at positions 9, 10, 11 from the 5’ end of the sense strand. In some embodiments, the other nucleotides of the sense strand are 2'-O-methyl modified nucleotides. In some embodiments, the antisense strand has five 2'-fluoro modified nucleotides, e.g., at positions 2, 5, 7, 14, 16 from the 5’ end of the antisense strand. In some embodiments, the antisense strand has five 2'-fluoro modified nucleotides, e.g., at positions 2, 5, 8, 14, 16 from the 5’ end of the antisense strand. In some embodiments, the antisense strand has five 2'-fluoro modified nucleotides, e.g., at positions 2, 3, 7, 14, 16 from the 5’ end of the antisense strand. In some embodiments, the other nucleotides of the antisense strand are 2'-O-methyl modified nucleotides.

[0073] In some embodiments, the 5’ end of the antisense strand has a phosphate analog, e.g., 5’-vinylphosphonate (5’-VP).

[0074] In some embodiments, the sense strand or the antisense strand comprises an abasic moiety or inverted abasic moiety, e.g., a moiety shown in Table 5.Table 5. Abasic or inverted abasic (iAb) moieties Structure ion of the sequences.

[0075] In some embodiments, the sense strand and the antisense strand have one or more modified internucleotide linkages. In some embodiments, the modified internucleotide linkage is phosphorothioate linkage. In some embodiments, the sense strand has four or five phosphorothioate linkages. In some embodiments, the antisense strand has four or five phosphorothioate linkages. In some embodiments, the sense strand and the antisense strand each has four or five phosphorothioate linkages. In some embodiments, the sense strand has four phosphorothioate linkages and the antisense strand has five phosphorothioate linkages.

[0076] Exemplary modified sense strand and antisense strand sequences of dsRNA targeting human SNCA mRNA are provided in Table 6a. Exemplary modified sense strand and antisense strand sequences of dsRNA targeting human MAPT mRNA are provided in Table 6b.

[0077] In some embodiments, the dsRNA comprises a sense strand that comprises a sequence that has 1, 2, or 3 differences from a sense stand sequence in Table 4a or 6a. In some embodiments, the dsRNA comprises an antisense strand that comprises a sequence that has 1, 2, or 3 differences from an antisense stand sequence in Table 4a or 6a.

[0078] In some embodiments, the dsRNA comprises a sense strand that comprises a sequence that has 1, 2, or 3 differences from a sense stand sequence in Table 4b or 6b. In some embodiments, the dsRNA comprises an antisense strand that comprises a sequence that has 1, 2, or 3 differences from an antisense stand sequence in Table 4b or 6b.Table 6a: Modified Nucleic Acid Sequences of dsRNA targeting human SNCA mRNA (SNCA siRNA) dsRNA SEQ ID Strand Oligo Sequence 5' to 3' No. NO 45 46 47 48 47 49 47 50 51 46 52 53 54 55 56 5758 59 60 59mC*mU*mGmUmAmCmAmAfGnfGmCmUmCmAmGmUmUmC*mC*mA, wherein n is the 61 S 21 abasic moiety in Table 10. 9 2 9“iAb” indicates inverted abasic moiety in Table 10; “S” means the sense strand; “AS” means the antisense strand. Table 6b: Modified Nucleic Acid Sequences of dsRNA targeting human MAPT mRNA (MAPT siRNA) dsRNA SEQ ID Strand Oligo Sequence 5' to 3' No. NO 3 4 5 6 7 8 9 0 1 2 3 4Note – The 5’ end of the AS may be substituted with 5’-vinylphosphonate. Abbreviations – “m” indicates 2’-OMe; “f” indicated 2’-fluoro; “*” indicates phosphorothioate linkage; “iAb” indicates inverted abasic moiety in Table 10; “S” means the sense strand; “AS” means the antisense strand.

[0079] In some embodiments, the dsRNA targets SNCA mRNA. In some embodiments, the sense strand and the antisense strand of the dsRNA comprise a pair of nucleic acid sequences selected from the group consisting of: (a) the sense strand comprises SEQ ID NO: 45, and the antisense strand comprises SEQ ID NO: 46; (b) the sense strand comprises SEQ ID NO: 47, and the antisense strand comprises SEQ ID NO: 48; (c) the sense strand comprises SEQ ID NO: 47, and the antisense strand comprises SEQ ID NO: 49; (d) the sense strand comprises SEQ ID NO: 47, and the antisense strand comprises SEQ ID NO: 50; (e) the sense strand comprises SEQ ID NO: 51, and the antisense strand comprises SEQ ID NO: 46; (f) the sense strand comprises SEQ ID NO: 52, and the antisense strand comprises SEQ ID NO: 53; (g) the sense strand comprises SEQ ID NO: 54, and the antisense strand comprises SEQ ID NO: 55; (h) the sense strand comprises SEQ ID NO: 56, and the antisense strand comprises SEQ ID NO: 57; (i) the sense strand comprises SEQ ID NO: 58, and the antisense strand comprises SEQ ID NO: 59; (j) the sense strand comprises SEQ ID NO: 60, and the antisense strand comprises SEQ ID NO: 59; (k) the sense strand comprises SEQ ID NO: 61, and the antisense strand comprises SEQ ID NO: 49; and (l) the sense strand comprises SEQ ID NO: 62, and the antisense strand comprises SEQ ID NO: 49.

[0080] In some embodiments, the sense strand and the antisense strand of the dsRNA have a pair of nucleic acid sequences selected from the group consisting of: (a) the sense strand consists of SEQ ID NO: 45, and the antisense strand consists of SEQ ID NO: 46; (b) the sense strand consists of SEQ ID NO: 47, and the antisense strand consists of SEQ ID NO: 48; (c) the sense strand consists of SEQ ID NO: 47, and the antisense strand consists of SEQ ID NO: 49; (d) the sense strand consists of SEQ ID NO: 47, and the antisense strand consists of SEQ ID NO: 50; (e) the sense strand consists of SEQ ID NO: 51, and the antisense strand consists of SEQ ID NO: 46; (f) the sense strand consists of SEQ ID NO: 52, and the antisense strand consists of SEQ ID NO: 53; (g) the sense strand consists of SEQ ID NO: 54, and the antisense strand consists of SEQ ID NO: 55; (h) the sense strand consists of SEQ ID NO: 56, and the antisense strand consists of SEQ ID NO: 57; (i) the sense strand consists of SEQ ID NO: 58, and the antisense strand consists of SEQ ID NO: 59; (j) the sense strand consists of SEQ ID NO: 60, and the antisense strand consists of SEQ ID NO: 59; (k) the sense strand consists of SEQ ID NO: 61, and the antisense strand consists of SEQ ID NO: 49; and (l) the sense strand consists of SEQ ID NO: 62, and the antisense strand consists of SEQ ID NO: 49.

[0081] In some embodiments, the dsRNA targets MAPT mRNA. In some embodiments, the sense strand and the antisense strand of the dsRNA comprise a pair of nucleic acid sequences selected from the group consisting of: (a) the sense strand comprises SEQ ID NO: 63, and the antisense strand comprises SEQ ID NO: 64;(b) the sense strand comprises SEQ ID NO: 65, and the antisense strand comprises SEQ ID NO: 66; (c) the sense strand comprises SEQ ID NO: 67, and the antisense strand comprises SEQ ID NO: 68; (d) the sense strand comprises SEQ ID NO: 69, and the antisense strand comprises SEQ ID NO: 70; (e) the sense strand comprises SEQ ID NO: 71, and the antisense strand comprises SEQ ID NO: 72; and (f) the sense strand comprises SEQ ID NO: 73, and the antisense strand comprises SEQ ID NO: 74.

[0082] In some embodiments, the sense strand and the antisense strand of the dsRNA have a pair of nucleic acid sequences selected from the group consisting of: (a) the sense strand consists of SEQ ID NO: 63, and the antisense strand consists of SEQ ID NO: 64; (b) the sense strand consists of SEQ ID NO: 65, and the antisense strand consists of SEQ ID NO: 66; (c) the sense strand consists of SEQ ID NO: 67, and the antisense strand consists of SEQ ID NO: 68; (d) the sense strand consists of SEQ ID NO: 69, and the antisense strand consists of SEQ ID NO: 70; (e) the sense strand consists of SEQ ID NO: 71, and the antisense strand consists of SEQ ID NO: 72; and (f) the sense strand consists of SEQ ID NO: 73, and the antisense strand consists of SEQ ID NO: 74.

[0083] The sense strand and antisense strand of dsRNA can be synthesized using any nucleic acid polymerization methods known in the art, for example, solid-phase synthesis by employing phosphoramidite chemistry methodology (e.g., Current Protocols in Nucleic Acid Chemistry, Beaucage, S.L. et al. (Edrs.), John Wiley & Sons, Inc., New York, NY, USA), H- phosphonate, phosphortriester chemistry, or enzymatic synthesis. Automated commercial synthesizers can be used, for example, MerMade™ 12 from LGC Biosearch Technologies, or other synthesizers from BioAutomation or Applied Biosystems. Phosphorothioate linkages canbe introduced using a sulfurizing reagent such as phenylacetyl disulfide or DDTT (((dimethylaminomethylidene) amino)-3H-l,2,4-dithiazaoline-3-thione). It is well known to use similar techniques and commercially available modified amidites and controlled-pore glass (CPG) products to synthesize modified oligonucleotides or conjugated oligonucleotides.

[0084] Purification methods can be used to exclude the unwanted impurities from the final oligonucleotide product. Commonly used purification techniques for single stranded oligonucleotides include reverse-phase ion pair high performance liquid chromatography (RP-IP- HPLC), capillary gel electrophoresis (CGE), anion exchange HPLC (AX-HPLC), and size exclusion chromatography (SEC). After purification, oligonucleotides can be analyzed by mass spectrometry and quantified by spectrophotometry at a wavelength of 260 nm. The sense strand and antisense strand can then be annealed to form a dsRNA. Pharmaceutical Composition

[0085] In another aspect, provided herein are pharmaceutical compositions comprising any of the human TfR binding proteins or conjugates described herein and a pharmaceutically acceptable carrier. Such pharmaceutical compositions can also comprise one or more pharmaceutically acceptable excipient, diluent, or carrier. Pharmaceutical compositions can be prepared by methods well known in the art (e.g., Remington: The Science and Practice of Pharmacy, 23rd edition (2020), A. Loyd et al., Academic Press). Method of Treatment and Therapeutic Use

[0086] In another aspect, provided herein are methods of treating a CNS disease, e.g., a neurodegenerative disease, in a patient in need thereof, and such the method comprises administering to the patient an effective amount of the human TfR binding protein or conjugate or a pharmaceutical composition described herein.

[0087] In a further aspect, provided herein are methods of treating a neurodegenerative synucleinopathy in a patient in need thereof, and such the method comprises administering to the patient an effective amount of the human TfR binding proteins or conjugate or a pharmaceutical composition described herein, e.g., a TBP-SNCA siRNA conjugate described herein or a pharmaceutical composition comprising such a TBP-SNCA siRNA conjugate. Exemplary neurodegenerative synucleinopathy includes, but are not limited to, Parkinson’s disease; multiplesystem atrophy; Lewy body dementia or dementia with Lewy bodies; pure autonomic failure; Alzheimer’s disease; Lewy body dysphagia; and incidental Lewy body disease. In some embodiments, the neurodegenerative synucleinopathy is selected from Parkinson’s disease, Alzheimer’s disease, multiple system atrophy, or Lewy body dementia. The human TfR binding protein or conjugate or a pharmaceutical composition can be administered to the patient intravenously or subcutaneously.

[0088] In a further aspect, provided herein are methods of treating a tauopathy in a patient in need thereof, and such the method comprises administering to the patient an effective amount of the human TfR binding proteins or conjugate or a pharmaceutical composition described herein, e.g., a TBP-MAPT siRNA conjugate described herein or a pharmaceutical composition comprising such a TBP-MAPT siRNA conjugate. Exemplary tauopathy includes, but are not limited to, Alzheimer’s disease, frontotemporal dementia (FTD), frontotemporal dementia with parkinsonism linked to chromosome 17 (FTDP-17), frontotemporal lobar degeneration (FTLD), behavioral variant frontotemporal dementia (bvFTD), nonfluent variant primary progressive aphasia (nfvPPA), Parkinson’s discase, Pick’s disease (PiD), primary progressive aphasia - semantic (PPA-S), primary progressive aphasia - logopenic (PPA-L), multiple system tauopathy with presenile dementia (MSTD), neurofibrillary tangle (NFT) dementia, FTD with motor neuron disease, progressive supranuclear palsy (PSP), amyotrophic lateral sclerosis / parkinsonism-dementia complex (ALS-PDC), argyrophilic grain dementia (AGD), British type amyloid angiopathy, cerebral amyloid angiopathy, chronic traumatic encephalopathy (CTE), corticobasal degeneration (CBD), Creutzfeldt-Jakob disease (CJD), dementia pugilistica, diffuse neurofibrillary tangles with calcification, Down’s syndrome, epilepsy, Gerstmann-Straussler-Scheinker disease, Hallervorden-Spatz disease, Huntington’s disease, inclusion body myositis, lead encephalopathy, Lytico-Bodig disease, meningioangiomatosis, multiple system atrophy, myotonic dystrophy, Niemann-Pick disease type C (NP-C), non-Guamanian motor neuron disease with neurofibrillary tangles, postencephalitic parkinsonism, prion protein cerebral amyloid angiopathy, progressive subcortical gliosis, tangle only dementia, tangle-predominant dementia, ganglioglioma, gangliocytoma, subacute sclerosingpan encephalitis, tuberous sclerosis, lipofuscinosis, primary age-related tauopathy (PART), or globular glial tauopathies (GGT). The human TfR bindingprotein or conjugate or a pharmaceutical composition can be administered to the patient intravenously or subcutaneously.

[0089] Human TfR binding protein or conjugate dosage regimens may be adjusted to provide the optimum desired response (e.g., a therapeutic response). For example, a single bolus may be administered, several divided doses may be administered over time, or the dose may be proportionally reduced or increased as indicated by the exigencies of the therapeutic situation.

[0090] Dosage values may vary with the type and severity of the condition to be alleviated. It is further understood that for any particular subject, specific dosage regimens should be adjusted over time according to the individual need and the professional judgment of the person administering or supervising the administration of the compositions.

[0091] In another aspect, provided herein are human TfR binding proteins or conjugates described herein or pharmaceutical compositions comprising such human TfR binding proteins or conjugates for use in a therapy. Also provided herein are human TfR binding proteins or conjugates described herein or pharmaceutical compositions comprising such human TfR binding proteins or conjugates (e.g., a TBP-SNCA siRNA conjugate described herein or a pharmaceutical composition comprising such a TBP-SNCA siRNA conjugate) for use in the treatment of a neurodegenerative synucleinopathy, e.g., Parkinson’s disease, Alzheimer’s disease, multiple system atrophy, or Lewy body dementia.

[0092] Also provided herein are human TfR binding proteins or conjugates described herein or pharmaceutical compositions comprising such human TfR binding proteins or conjugates (e.g., a TBP-MAPT siRNA conjugate described herein or a pharmaceutical composition comprising such a TBP-MAPT siRNA conjugate) for use in the treatment of a tauopathy, e.g., Alzheimer’s disease, frontotemporal dementia (FTD), frontotemporal dementia with parkinsonism linked to chromosome 17 (FTDP-17), frontotemporal lobar degeneration (FTLD), behavioral variant frontotemporal dementia (bvFTD), nonfluent variant primary progressive aphasia (nfvPPA), Parkinson’s discase, Pick’s disease (PiD), primary progressive aphasia - semantic (PPA-S), primary progressive aphasia - logopenic (PPA-L), multiple system tauopathy with presenile dementia (MSTD), neurofibrillary tangle (NFT) dementia, FTD with motor neuron disease, progressive supranuclear palsy (PSP), amyotrophic lateral sclerosis / parkinsonism-dementia complex (ALS-PDC), argyrophilic grain dementia (AGD), British type amyloid angiopathy, cerebral amyloid angiopathy, chronic traumatic encephalopathy(CTE), corticobasal degeneration (CBD), Creutzfeldt-Jakob disease (CJD), dementia pugilistica, diffuse neurofibrillary tangles with calcification, Down’s syndrome, epilepsy, Gerstmann- Straussler-Scheinker disease, Hallervorden-Spatz disease, Huntington’s disease, inclusion body myositis, lead encephalopathy, Lytico-Bodig disease, meningioangiomatosis, multiple system atrophy, myotonic dystrophy, Niemann-Pick disease type C (NP-C), non-Guamanian motor neuron disease with neurofibrillary tangles, postencephalitic parkinsonism, prion protein cerebral amyloid angiopathy, progressive subcortical gliosis, tangle only dementia, tangle-predominant dementia, ganglioglioma, gangliocytoma, subacute sclerosingpan encephalitis, tuberous sclerosis, lipofuscinosis, primary age-related tauopathy (PART), or globular glial tauopathies (GGT).

[0093] In another aspect, provided herein are uses of human TfR binding proteins or conjugates described herein in the manufacture of a medicament for treating a CNS disease, e.g., a neurodegenerative disease. In some embodiments, the neurodegenerative disease is a neurodegenerative synucleinopathy, e.g., Parkinson’s disease, Alzheimer’s disease, multiple system atrophy, or Lewy body dementia. In some embodiments, the neurodegenerative disease is a tauopathy, e.g., Alzheimer’s disease, frontotemporal dementia (FTD), frontotemporal dementia with parkinsonism linked to chromosome 17 (FTDP-17), frontotemporal lobar degeneration (FTLD), behavioral variant frontotemporal dementia (bvFTD), nonfluent variant primary progressive aphasia (nfvPPA), Parkinson’s discase, Pick’s disease (PiD), primary progressive aphasia - semantic (PPA-S), primary progressive aphasia - logopenic (PPA-L), multiple system tauopathy with presenile dementia (MSTD), neurofibrillary tangle (NFT) dementia, FTD with motor neuron disease, progressive supranuclear palsy (PSP), amyotrophic lateral sclerosis / parkinsonism-dementia complex (ALS-PDC), argyrophilic grain dementia (AGD), British type amyloid angiopathy, cerebral amyloid angiopathy, chronic traumatic encephalopathy (CTE), corticobasal degeneration (CBD), Creutzfeldt-Jakob disease (CJD), dementia pugilistica, diffuse neurofibrillary tangles with calcification, Down’s syndrome, epilepsy, Gerstmann- Straussler-Scheinker disease, Hallervorden-Spatz disease, Huntington’s disease, inclusion body myositis, lead encephalopathy, Lytico-Bodig disease, meningioangiomatosis, multiple system atrophy, myotonic dystrophy, Niemann-Pick disease type C (NP-C), non-Guamanian motor neuron disease with neurofibrillary tangles, postencephalitic parkinsonism, prion protein cerebral amyloid angiopathy, progressive subcortical gliosis, tangle only dementia, tangle-predominantdementia, ganglioglioma, gangliocytoma, subacute sclerosingpan encephalitis, tuberous sclerosis, lipofuscinosis, primary age-related tauopathy (PART), or globular glial tauopathies (GGT). Definitions

[0094] As used herein, the terms “a,” “an,” “the,” and similar terms used in the context of the present disclosure (especially in the context of the claims) are to be construed to cover both the singular and plural unless otherwise indicated herein or clearly contradicted by the context.

[0095] As used herein, the term “alkyl” means saturated linear or branched-chain monovalent hydrocarbon radical, containing the indicated number of carbon atoms. For example, “C1-C20alkyl” means a radical having 1-20 carbon atoms in a linear or branched arrangement.

[0096] The term “antibody,” as used herein, refers to a molecule that binds an antigen. Embodiments of an antibody include a monoclonal antibody, polyclonal antibody, human antibody, humanized antibody, chimeric antibody, heterodimeric antibody, bispecific or multispecific antibody, or conjugated antibody . The antibodies can be of any class (e.g., IgG, IgE, IgM, IgD, IgA), and any subclass (e.g., IgG1, IgG2, IgG3, IgG4).

[0097] An immunoglobulin G (IgG) type antibody comprised of four polypeptide chains: two heavy chains (HC) and two light chains (LC) that are cross-linked via inter-chain disulfide bonds. The amino-terminal portion of each of the four polypeptide chains includes a variable region of about 100-125 or more amino acids primarily responsible for antigen recognition. The carboxyl-terminal portion of each of the four polypeptide chains contains a constant region primarily responsible for effector function. Each heavy chain is comprised of a heavy chain variable region (VH) and a heavy chain constant region. Each light chain is comprised of a light chain variable region (VL) and a light chain constant region. The IgG isotype may be further divided into subclasses (e.g., IgG1, IgG2, IgG3, and IgG4).

[0098] The VH and VL regions can be further subdivided into regions of hyper- variability, termed complementarity determining regions (CDRs), interspersed with regions that are more conserved, termed framework regions (FR). The CDRs are exposed on the surface of the protein and are important regions of the antibody for antigen binding specificity. Each VH and VL is composed of three CDRs and four FRs, arranged from amino-terminus to carboxyl- terminus in the following order: FR1, CDR1, FR2, CDR2, FR3, CDR3, FR4. Herein, the threeCDRs of the heavy chain are referred to as “HCDR1, HCDR2, and HCDR3” and the three CDRs of the light chain are referred to as “LCDR1, LCDR2 and LCDR3”. The CDRs contain most of the residues that form specific interactions with the antigen. Assignment of amino acid residues to the CDRs may be done according to the well-known schemes, including those described in Kabat (Kabat et al., “Sequences of Proteins of Immunological Interest,” National Institutes of Health, Bethesda, Md. (1991)), Chothia (Chothia et al., “Canonical structures for the hypervariable regions of immunoglobulins”, Journal of Molecular Biology, 196, 901-917 (1987); Al-Lazikani et al., “Standard conformations for the canonical structures of immunoglobulins”, Journal of Molecular Biology, 273, 927-948 (1997)), North (North et al., “A New Clustering of Antibody CDR Loop Conformations”, Journal of Molecular Biology, 406, 228-256 (2011)), or IMGT (the international ImMunoGeneTics database available on at www.imgt.org; see Lefranc et al., Nucleic Acids Res. 1999; 27:209-212).

[0099] Embodiments of the present disclosure also include antibody fragments or antigen-binding fragments that, as used herein, comprise at least a portion of an antibody retaining the ability to specifically interact with an antigen or an epitope of the antigen, such as Fab, Fab’, F(ab’)2, Fv fragments, scFv antibody fragments, scFab, disulfide-linked Fvs (sdFv), a Fd fragment. [000100] The term “antigen binding domain”, as used herein, refers to a portion of an antibody or antibody fragment that binds an antigen or an epitope of the antigen. For example, “TfR binding domain” refers to a portion of an antibody or antibody fragment that binds TfR or an epitope of TfR. [000101] The term “heterodimeric antibody”, as used herein, refers to an antibody that comprises two distinct antigen-binding domains. [000102] As used herein, “antisense strand” means a single-stranded oligonucleotide that is complementary to a region of a target sequence. Likewise, and as used herein, “sense strand” means a single-stranded oligonucleotide that is complementary to a region of an antisense strand. [000103] The terms “bind” and “binds” as used herein are intended to mean, unless indicated otherwise, the ability of a protein or molecule to form a chemical bond or attractive interaction with another protein or molecule, which results in proximity of the two proteins or molecules as determined by common methods known in the art.[000104] As used herein, “complementary” means a structural relationship between two nucleotides (e.g., on two opposing nucleic acids or on opposing regions of a single nucleic acid strand, e.g., a hairpin) that permits the two nucleotides to form base pairs with one another. For example, a purine nucleotide of one nucleic acid that is complementary to a pyrimidine nucleotide of an opposing nucleic acid may base pair together by forming hydrogen bonds with one another. Complementary nucleotides can base pair in the Watson-Crick manner or in any other manner that allows for the formation of stable duplexes. Likewise, two nucleic acids may have regions of multiple nucleotides that are complementary with each other to form regions of complementarity, as described herein. [000105] As used herein, “duplex,” in reference to nucleic acids or oligonucleotides, means a structure formed through complementary base pairing of two antiparallel sequences of nucleotides (i.e., in opposite directions), whether formed by two separate nucleic acid strands or by a single, folded strand (e.g., via a hairpin). [000106] An “effective amount” refers to an amount necessary (for periods of time and for the means of administration) to achieve the desired therapeutic result. An effective amount of a protein or conjugate may vary according to factors such as the disease state, age, sex, and weight of the individual, and the ability of the protein or conjugate to elicit a desired response in the individual. An effective amount is also one in which any toxic or detrimental effects of the protein or conjugate are outweighed by the therapeutically beneficial effects. [000107] As referred to herein, the term “epitope” refers to the amino acid residues, of an antigen, that are bound by an antibody. An epitope can be a linear epitope, a conformational epitope, or a hybrid epitope. The term “epitope” may be used in reference to a structural epitope. A structural epitope, according to some embodiments, may be used to describe the region of an antigen which is covered by an antibody or antigen binding protein. In some embodiments, a structural epitope may describe the amino acid residues of the antigen that are within a specified proximity (e.g., within a specified number of Angstroms) of an amino acid residue of the antibody or antigen binding protein. The term “epitope” may also be used in reference to a functional epitope. A functional epitope, according to some embodiments, may be used to describe amino acid residues of the antigen that interact with amino acid residues of the antibody or antigen binding protein in a manner contributing to the binding energy between the antigen and the antibody or antigen binding protein.[000108] An epitope can be determined according to different experimental techniques, also called “epitope mapping techniques.” It is understood that the determination of an epitope may vary based on the different epitope mapping techniques used and may also vary with the different experimental conditions used, e.g., due to the conformational changes or cleavages of the antigen induced by specific experimental conditions. Epitope mapping techniques are known in the art (e.g., Rockberg and Nilvebrant, Epitope Mapping Protocols: Methods in Molecular Biology, Humana Press, 3rded. 2018), including but not limited to, X-ray crystallography, nuclear magnetic resonance (NMR) spectroscopy, site-directed mutagenesis, species swap mutagenesis, alanine-scanning mutagenesis, hydrogen-deuterium exchange (HDX) and cross- blocking assays. [000109] The term “Fc region” as used herein refers to a polypeptide comprising the CH2 and CH3 domains of a constant region of an immunoglobulin, e.g., IgG1, IgG2, IgG3, or IgG4. Optionally, the Fc region may include a portion of the hinge region or the entire hinge region of an immunoglobulin, e.g., IgG1, IgG2, IgG3, or IgG4. In some embodiments, the Fc region is a human IgG Fc region, e.g., a human IgG1 Fc region, human IgG2 Fc region, human IgG3 Fc region or human IgG4 Fc region. In some embodiments, the Fc region is a modified IgG Fc region with reduced or eliminated effector functions compared to the corresponding wild type IgG Fc region. The numbering of the residues in the Fc region is based on the EU index as described in Kabat (Kabat et al, Sequences of Proteins of Immunological Interest, 5th edition, Bethesda, MD: U.S. Dept. of Health and Human Services, Public Health Service, National Institutes of Health, 1991). The boundaries of the Fc region of an immunoglobulin heavy chain might vary, and the human IgG heavy chain Fc region is usually defined as the stretch from the N-terminus of the CH2 domain (e.g., the amino acid residue at position 231 according to the EU index numbering) to the C-terminus of the CH3 domain (or the C-terminus of the immunoglobulin). [000110] The term “knockdown” or “expression knockdown” refers to reduced mRNA or protein expression of a gene after treatment of a reagent. [000111] As used herein, “modified internucleotide linkage” means an internucleotide linkage having one or more chemical modifications when compared with a reference internucleotide linkage having a phosphodiester bond. A modified internucleotide linkage can bea non-naturally occurring linkage. In some embodiments, the modified internucleotide linkage is phosphorothioate linkage. [000112] As used herein, “modified nucleotide” refers to a nucleotide having one or more chemical modifications when compared with a corresponding reference nucleotide selected from: adenine ribonucleotide, guanine ribonucleotide, cytosine ribonucleotide, uracil ribonucleotide, adenine deoxyribonucleotide, guanine deoxyribonucleotide, cytosine deoxyribonucleotide, and thymidine deoxyribonucleotide. A modified nucleotide can have, for example, one or more chemical modification in its sugar, nucleobase, and / or phosphate group. Additionally, or alternatively, a modified nucleotide can have one or more chemical moieties conjugated to a corresponding reference nucleotide. In some embodiments, the modified nucleotide is a 2'-fluoro modified nucleotide, 2'-O-methyl modified nucleotide, or 2'-O-alkyl (e.g., 2’-O-C16alkyl) modified nucleotide. In some embodiments, the modified nucleotide has a phosphate analog, e.g., 5’-vinylphosphonate. In some embodiments, the modified nucleotide has an abasic moiety or inverted abasic moiety, e.g., a moiety shown in Table 10. [000113] As used herein, the term “neurodegenerative synucleinopathy” refers to a neurodegenerative disorder characterized by fibrillary aggregates of alpha-synuclein protein in the cytoplasm of selective populations of neurons and glia in the central and / or peripheral nervous systems. [000114] As used herein, “nucleotide” means an organic compound having a nucleoside (a nucleobase, e.g., adenine, cytosine, guanine, thymine, or uracil, and a pentose sugar, e.g., ribose or 2'-deoxyribose) linked to a phosphate group. A “nucleotide” can serve as a monomeric unit of nucleic acid polymers such as deoxyribonucleic acid (DNA) and ribonucleic acid (RNA). [000115] As used herein, a “null arm” means an antibody arm that does not bind any known human target. [000116] As used herein, “oligonucleotide” means a polymer of linked nucleotides, each of which can be modified or unmodified. An oligonucleotide is typically less than about 100 nucleotides in length. [000117] As used herein, “overhang” means the unpaired nucleotide or nucleotides that protrude from the duplex structure of a double stranded oligonucleotide. An overhang may include one or more unpaired nucleotides extending from a duplex region at the 5’ terminus or 3’terminus of a double stranded oligonucleotide. The overhang can be a 3’ or 5’ overhang on the antisense strand or sense strand of a double stranded oligonucleotide. [000118] The term “patient”, as used herein, refers to a human patient. [000119] As used herein, “phosphate analog” means a chemical moiety that mimics the electrostatic and / or steric properties of a phosphate group. In some embodiments, a phosphate analog is positioned at the 5’ terminal nucleotide of an oligonucleotide in place of a 5’- phosphate, which is often susceptible to enzymatic removal. A 5’ phosphate analog can include a phosphatase-resistant linkage. Examples of phosphate analogs include 5’ methylene phosphonate (5’-MP) and 5’-(E)-vinylphosphonate (5’-VP). In some embodiments, the phosphate analog is 5’-VP. [000120] The term “% sequence identity” or “percentage sequence identity” with respect to a reference nucleic acid sequence is defined as the percentage of nucleotides, nucleosides, or nucleobases in a candidate sequence that are identical with the nucleotides, nucleosides, or nucleobases in the reference nucleic acid sequence, after optimally aligning the sequences and introducing gaps or overhangs, if necessary, to achieve the maximum percent sequence identity. Alignment for purposes of determining percent nucleic acid sequence identity can be achieved in various ways that are within the skill in the art, for instance, using publicly available computer software programs, for example, those described in Current Protocols in Molecular Biology (Ausubel et al., eds., 1987, Supp. 30, section 7.7.18, Table 7.7.1), and including BLAST, BLAST-2, ALIGN, Megalign (DNASTAR), Clustal W2.0 or Clustal X2.0 software. Those skilled in the art can determine appropriate parameters for measuring alignment, including any algorithms needed to achieve maximal alignment over the full length of the sequences being compared. Percentage of “sequence identity” can be determined by comparing two optimally aligned sequences over a comparison window, where the fragment of the nucleic acid sequence in the comparison window may comprise additions or deletions (e.g., gaps or overhangs) as compared to the reference sequence (which does not comprise additions or deletions) for optimal alignment of the two sequences. The percentage can be calculated by determining the number of positions at which the identical nucleotide, nucleoside, or nucleobase occurs in both sequences to yield the number of matched positions, dividing the number of matched positions by the total number of positions in the window of comparison, and multiplying the result by 100 to yield thepercentage of sequence identity. The output is the percent identity of the subject sequence with respect to the query sequence. [000121] The term “polypeptide” or “protein”, as used herein, refers to a polymer of amino acid residues. The term applies to polymers comprising naturally occurring amino acids and polymers comprising one or more non-naturally occurring amino acids. [000122] As used herein, “strand” refers to a single, contiguous sequence of nucleotides linked together through internucleotide linkages (e.g., phosphodiester linkages or phosphorothioate linkages). A strand can have two free ends (e.g., a 5’ end and a 3’ end). [000123] As used herein, “SNCA” refers to an alpha-synuclein (SNCA) mRNA, protein, or polypeptide. The nucleic acid sequence of a human SNCA mRNA transcript can be found at NM_000345.4: 1 GGCGACGACC AGAAGGGGCC CAAGAGAGGG GGCGAGCGAC CGAGCGCCGC GACGCGGAAG 61 TGAGGTGCGT GCGGGCTGCA GCGCAGACCC CGGCCCGGCC CCTCCGAGAG CGTCCTGGGC 121 GCTCCCTCAC GCCTTGCCTT CAAGCCTTCT GCCTTTCCAC CCTCGTGAGC GGAGAACTGG 181 GAGTGGCCAT TCGACGACAG TGTGGTGTAA AGGAATTCAT TAGCCATGGA TGTATTCATG 241 AAAGGACTTT CAAAGGCCAA GGAGGGAGTT GTGGCTGCTG CTGAGAAAAC CAAACAGGGT 301 GTGGCAGAAG CAGCAGGAAA GACAAAAGAG GGTGTTCTCT ATGTAGGCTC CAAAACCAAG 361 GAGGGAGTGG TGCATGGTGT GGCAACAGTG GCTGAGAAGA CCAAAGAGCA AGTGACAAAT 421 GTTGGAGGAG CAGTGGTGAC GGGTGTGACA GCAGTAGCCC AGAAGACAGT GGAGGGAGCA 481 GGGAGCATTG CAGCAGCCAC TGGCTTTGTC AAAAAGGACC AGTTGGGCAA GAATGAAGAA 541 GGAGCCCCAC AGGAAGGAAT TCTGGAAGAT ATGCCTGTGG ATCCTGACAA TGAGGCTTAT 601 GAAATGCCTT CTGAGGAAGG GTATCAAGAC TACGAACCTG AAGCCTAAGA AATATCTTTG 661 CTCCCAGTTT CTTGAGATCT GCTGACAGAT GTTCCATCCT GTACAAGTGC TCAGTTCCAA 721 TGTGCCCAGT CATGACATTT CTCAAAGTTT TTACAGTGTA TCTCGAAGTC TTCCATCAGC 781 AGTGATTGAA GTATCTGTAC CTGCCCCCAC TCAGCATTTC GGTGCTTCCC TTTCACTGAA 841 GTGAATACAT GGTAGCAGGG TCTTTGTGTG CTGTGGATTT TGTGGCTTCA ATCTACGATG 901 TTAAAACAAA TTAAAAACAC CTAAGTGACT ACCACTTATT TCTAAATCCT CACTATTTTT 961 TTGTTGCTGT TGTTCAGAAG TTGTTAGTGA TTTGCTATCA TATATTATAA GATTTTTAGG 1021 TGTCTTTTAA TGATACTGTC TAAGAATAAT GACGTATTGT GAAATTTGTT AATATATATA 1081 ATACTTAAAA ATATGTGAGC ATGAAACTAT GCACCTATAA ATACTAAATA TGAAATTTTA 1141 CCATTTTGCG ATGTGTTTTA TTCACTTGTG TTTGTATATA AATGGTGAGA ATTAAAATAA 1201 AACGTTATCT CATTGCAAAA ATATTTTATT TTTATCCCAT CTCACTTTAA TAATAAAAAT 1261 CATGCTTATA AGCAACATGA ATTAAGAACT GACACAAAGG ACAAAAATAT AAAGTTATTA 1321 ATAGCCATTT GAAGAAGGAG GAATTTTAGA AGAGGTAGAG AAAATGGAAC ATTAACCCTA 1381 CACTCGGAAT TCCCTGAAGC AACACTGCCA GAAGTGTGTT TTGGTATGCA CTGGTTCCTT 1441 AAGTGGCTGT GATTAATTAT TGAAAGTGGG GTGTTGAAGA CCCCAACTAC TATTGTAGAG 1501 TGGTCTATTT CTCCCTTCAA TCCTGTCAAT GTTTGCTTTA CGTATTTTGG GGAACTGTTG 1561 TTTGATGTGT ATGTGTTTAT AATTGTTATA CATTTTTAAT TGAGCCTTTT ATTAACATAT 1621 ATTGTTATTT TTGTCTCGAA ATAATTTTTT AGTTAAAATC TATTTTGTCT GATATTGGTG 1681 TGAATGCTGT ACCTTTCTGA CAATAAATAA TATTCGACCA TGAATAAAAA AAAAAAAAAA 1741 GTGGGTTCCC GGGAACTAAG CAGTGTAGAA GATGATTTTG ACTACACCCT CCTTAGAGAG 1801 CCATAAGACA CATTAGCACA TATTAGCACA TTCAAGGCTC TGAGAGAATG TGGTTAACTT 1861 TGTTTAACTC AGCATTCCTC ACTTTTTTTT TTTAATCATC AGAAATTCTC TCTCTCTCTC 1921 TCTCTTTTTC TCTCGCTCTC TTTTTTTTTT TTTTTTTACA GGAAATGCCT TTAAACATCG 1981 TTGGAACTAC CAGAGTCACC TTAAAGGAGA TCAATTCTCT AGACTGATAA AAATTTCATG 2041 GCCTCCTTTA AATGTTGCCA AATATATGAA TTCTAGGATT TTTCCTTAGG AAAGGTTTTT 2101 CTCTTTCAGG GAAGATCTAT TAACTCCCCA TGGGTGCTGA AAATAAACTT GATGGTGAAA2161 AACTCTGTAT AAATTAATTT AAAAATTATT TGGTTTCTCT TTTTAATTAT TCTGGGGCAT 2221 AGTCATTTCT AAAAGTCACT AGTAGAAAGT ATAATTTCAA GACAGAATAT TCTAGACATG 2281 CTAGCAGTTT ATATGTATTC ATGAGTAATG TGATATATAT TGGGCGCTGG TGAGGAAGGA 2341 AGGAGGAATG AGTGACTATA AGGATGGTTA CCATAGAAAC TTCCTTTTTT ACCTAATTGA 2401 AGAGAGACTA CTACAGAGTG CTAAGCTGCA TGTGTCATCT TACACTAGAG AGAAATGGTA 2461 AGTTTCTTGT TTTATTTAAG TTATGTTTAA GCAAGGAAAG GATTTGTTAT TGAACAGTAT 2521 ATTTCAGGAA GGTTAGAAAG TGGCGGTTAG GATATATTTT AAATCTACCT AAAGCAGCAT 2581 ATTTTAAAAA TTTAAAAGTA TTGGTATTAA ATTAAGAAAT AGAGGACAGA ACTAGACTGA 2641 TAGCAGTGAC CTAGAACAAT TTGAGATTAG GAAAGTTGTG ACCATGAATT TAAGGATTTA 2701 TGTGGATACA AATTCTCCTT TAAAGTGTTT CTTCCCTTAA TATTTATCTG ACGGTAATTT 2761 TTGAGCAGTG AATTACTTTA TATATCTTAA TAGTTTATTT GGGACCAAAC ACTTAAACAA 2821 AAAGTTCTTT AAGTCATATA AGCCTTTTCA GGAAGCTTGT CTCATATTCA CTCCCGAGAC 2881 ATTCACCTGC CAAGTGGCCT GAGGATCAAT CCAGTCCTAG GTTTATTTTG CAGACTTACA 2941 TTCTCCCAAG TTATTCAGCC TCATATGACT CCACGGTCGG CTTTACCAAA ACAGTTCAGA 3001 GTGCACTTTG GCACACAATT GGGAACAGAA CAATCTAATG TGTGGTTTGG TATTCCAAGT 3061 GGGGTCTTTT TCAGAATCTC TGCACTAGTG TGAGATGCAA ACATGTTTCC TCATCTTTCT 3121 GGCTTATCCA GTATGTAGCT ATTTGTGACA TAATAAATAT ATACATATAT GAAAATA (SEQ ID NO: 75). The amino acid sequence of a human SNCA protein can be found at NP_000336.1: 1 MDVFMKGLSK AKEGVVAAAE KTKQGVAEAA GKTKEGVLYV GSKTKEGVVH GVATVAEKTK 61 EQVTNVGGAV VTGVTAVAQK TVEGAGSIAA ATGFVKKDQL GKNEEGAPQE GILEDMPVDP 121 DNEAYEMPSE EGYQDYEPEA (SEQ ID NO: 76). [000124] The nucleic acid sequence of a mouse SNCA mRNA transcript can be found at NM_001042451.2; and the amino acid sequence of a mouse SNCA protein can be found at NP_001035916.1. The nucleic acid sequence of a rat SNCA mRNA transcript can be found at NM_019169.3; and the amino acid sequence of a rat SNCA protein can be found at NP_062042.1. The nucleic acid sequence of a monkey SNCA mRNA transcript can be found at XM_005555422.2; and the amino acid sequence of a monkey SNCA protein can be found at XP_005555479.1. [000125] As used herein, “MAPT” refers to a human MAPT mRNA transcript, encoding a microtubule associated protein Tau. The nucleotide sequences of human MAPT transcript variants and amino acid sequences of human Tau protein isoforms can be found at: i. MAPT transcript variant 1 → Tau protein isoform 1: NM_016835.5 (nucleotide sequence) → NP_058519.3 (amino acid sequence); ii. MAPT transcript variant 2 → Tau protein isoform 2: NM_005910.6 (nucleotide sequence) → NP_005901.2 (amino acid sequence); iii. MAPT transcript variant 3 → Tau protein isoform 3: NM_016834.5 (nucleotide sequence) → NP_058518.1 (amino acid sequence);iv. MAPT transcript variant 4 → Tau protein isoform 4: NM_016841.5 (nucleotide sequence) → NP_058525.1 (amino acid sequence); v. MAPT transcript variant 5 → Tau protein isoform 5: NM_001123067.4 (nucleotide sequence) → NP_001116539.1 (amino acid sequence); vi. MAPT transcript variant 6 → Tau protein isoform 6: NM_001123066.4 (nucleotide sequence) → NP_001116538.2 (amino acid sequence); vii. MAPT transcript variant 7 → Tau protein isoform 7: NM_001203251.2 (nucleotide sequence) → NP_001190180.1 (amino acid sequence); viii. MAPT transcript variant 8 → Tau protein isoform 8: NM_001203252.2 (nucleotide sequence) → NP_001190181.1 (amino acid sequence); ix. MAPT transcript variant 9 → Tau protein isoform 9: NM_001377265.1 (nucleotide sequence) → NP_001364194.1 (amino acid sequence); x. MAPT transcript variant 10 → Tau protein isoform 10: NM_001377266.1 (nucleotide sequence) → NP_001364195.1 (amino acid sequence); xi. MAPT transcript variant 11 → Tau protein isoform 11: NM_001377267.1 (nucleotide sequence) → NP_001364196.1 (amino acid sequence); xii. MAPT transcript variant 12 → Tau protein isoform 4: NM_001377268.1 (nucleotide sequence) → NP_001364197.1 (amino acid sequence). [000126] The nucleotide sequence of the human MAPT transcript variant 6 (encoding 2N4R Tau) can be found at NM_001123066.4: 1 GCAGTCACCG CCACCCACCA GCTCCGGCAC CAACAGCAGC GCCGCTGCCA CCGCCCACCT 61 TCTGCCGCCG CCACCACAGC CACCTTCTCC TCCTCCGCTG TCCTCTCCCG TCCTCGCCTC 121 TGTCGACTAT CAGGTGAACT TTGAACCAGG ATGGCTGAGC CCCGCCAGGA GTTCGAAGTG 181 ATGGAAGATC ACGCTGGGAC GTACGGGTTG GGGGACAGGA AAGATCAGGG GGGCTACACC 241 ATGCACCAAG ACCAAGAGGG TGACACGGAC GCTGGCCTGA AAGAATCTCC CCTGCAGACC 301 CCCACTGAGG ACGGATCTGA GGAACCGGGC TCTGAAACCT CTGATGCTAA GAGCACTCCA 361 ACAGCGGAAG ATGTGACAGC ACCCTTAGTG GATGAGGGAG CTCCCGGCAA GCAGGCTGCC 421 GCGCAGCCCC ACACGGAGAT CCCAGAAGGA ACCACAGCTG AAGAAGCAGG CATTGGAGAC 481 ACCCCCAGCC TGGAAGACGA AGCTGCTGGT CACGTGACCC AAGAGCCTGA AAGTGGTAAG 541 GTGGTCCAGG AAGGCTTCCT CCGAGAGCCA GGCCCCCCAG GTCTGAGCCA CCAGCTCATG 601 TCCGGCATGC CTGGGGCTCC CCTCCTGCCT GAGGGCCCCA GAGAGGCCAC ACGCCAACCT 661 TCGGGGACAG GACCTGAGGA CACAGAGGGC GGCCGCCACG CCCCTGAGCT GCTCAAGCAC 721 CAGCTTCTAG GAGACCTGCA CCAGGAGGGG CCGCCGCTGA AGGGGGCAGG GGGCAAAGAG 781 AGGCCGGGGA GCAAGGAGGA GGTGGATGAA GACCGCGACG TCGATGAGTC CTCCCCCCAA 841 GACTCCCCTC CCTCCAAGGC CTCCCCAGCC CAAGATGGGC GGCCTCCCCA GACAGCCGCC 901 AGAGAAGCCA CCAGCATCCC AGGCTTCCCA GCGGAGGGTG CCATCCCCCT CCCTGTGGAT 961 TTCCTCTCCA AAGTTTCCAC AGAGATCCCA GCCTCAGAGC CCGACGGGCC CAGTGTAGGG 1021 CGGGCCAAAG GGCAGGATGC CCCCCTGGAG TTCACGTTTC ACGTGGAAAT CACACCCAAC 1081 GTGCAGAAGG AGCAGGCGCA CTCGGAGGAG CATTTGGGAA GGGCTGCATT TCCAGGGGCC 1141 CCTGGAGAGG GGCCAGAGGC CCGGGGCCCC TCTTTGGGAG AGGACACAAA AGAGGCTGAC1201 CTTCCAGAGC CCTCTGAAAA GCAGCCTGCT GCTGCTCCGC GGGGGAAGCC CGTCAGCCGG 1261 GTCCCTCAAC TCAAAGCTCG CATGGTCAGT AAAAGCAAAG ACGGGACTGG AAGCGATGAC 1321 AAAAAAGCCA AGACATCCAC ACGTTCCTCT GCTAAAACCT TGAAAAATAG GCCTTGCCTT 1381 AGCCCCAAAC ACCCCACTCC TGGTAGCTCA GACCCTCTGA TCCAACCCTC CAGCCCTGCT 1441 GTGTGCCCAG AGCCACCTTC CTCTCCTAAA TACGTCTCTT CTGTCACTTC CCGAACTGGC 1501 AGTTCTGGAG CAAAGGAGAT GAAACTCAAG GGGGCTGATG GTAAAACGAA GATCGCCACA 1561 CCGCGGGGAG CAGCCCCTCC AGGCCAGAAG GGCCAGGCCA ACGCCACCAG GATTCCAGCA 1621 AAAACCCCGC CCGCTCCAAA GACACCACCC AGCTCTGCGA CTAAGCAAGT CCAGAGAAGA 1681 CCACCCCCTG CAGGGCCCAG ATCTGAGAGA GGTGAACCTC CAAAATCAGG GGATCGCAGC 1741 GGCTACAGCA GCCCCGGCTC CCCAGGCACT CCCGGCAGCC GCTCCCGCAC CCCGTCCCTT 1801 CCAACCCCAC CCACCCGGGA GCCCAAGAAG GTGGCAGTGG TCCGTACTCC ACCCAAGTCG 1861 CCGTCTTCCG CCAAGAGCCG CCTGCAGACA GCCCCCGTGC CCATGCCAGA CCTGAAGAAT 1921 GTCAAGTCCA AGATCGGCTC CACTGAGAAC CTGAAGCACC AGCCGGGAGG CGGGAAGGTG 1981 CAGATAATTA ATAAGAAGCT GGATCTTAGC AACGTCCAGT CCAAGTGTGG CTCAAAGGAT 2041 AATATCAAAC ACGTCCCGGG AGGCGGCAGT GTGCAAATAG TCTACAAACC AGTTGACCTG 2101 AGCAAGGTGA CCTCCAAGTG TGGCTCATTA GGCAACATCC ATCATAAACC AGGAGGTGGC 2161 CAGGTGGAAG TAAAATCTGA GAAGCTTGAC TTCAAGGACA GAGTCCAGTC GAAGATTGGG 2221 TCCCTGGACA ATATCACCCA CGTCCCTGGC GGAGGAAATA AAAAGATTGA AACCCACAAG 2281 CTGACCTTCC GCGAGAACGC CAAAGCCAAG ACAGACCACG GGGCGGAGAT CGTGTACAAG 2341 TCGCCAGTGG TGTCTGGGGA CACGTCTCCA CGGCATCTCA GCAATGTCTC CTCCACCGGC 2401 AGCATCGACA TGGTAGACTC GCCCCAGCTC GCCACGCTAG CTGACGAGGT GTCTGCCTCC 2461 CTGGCCAAGC AGGGTTTGTG ATCAGGCCCC TGGGGCGGTC AATAATTGTG GAGAGGAGAG 2521 AATGAGAGAG TGTGGAAAAA AAAAGAATAA TGACCCGGCC CCCGCCCTCT GCCCCCAGCT 2581 GCTCCTCGCA GTTCGGTTAA TTGGTTAATC ACTTAACCTG CTTTTGTCAC TCGGCTTTGG 2641 CTCGGGACTT CAAAATCAGT GATGGGAGTA AGAGCAAATT TCATCTTTCC AAATTGATGG 2701 GTGGGCTAGT AATAAAATAT TTAAAAAAAA ACATTCAAAA ACATGGCCAC ATCCAACATT 2761 TCCTCAGGCA ATTCCTTTTG ATTCTTTTTT CTTCCCCCTC CATGTAGAAG AGGGAGAAGG 2821 AGAGGCTCTG AAAGCTGCTT CTGGGGGATT TCAAGGGACT GGGGGTGCCA ACCACCTCTG 2881 GCCCTGTTGT GGGGGTGTCA CAGAGGCAGT GGCAGCAACA AAGGATTTGA AACTTGGTGT 2941 GTTCGTGGAG CCACAGGCAG ACGATGTCAA CCTTGTGTGA GTGTGACGGG GGTTGGGGTG 3001 GGGCGGGAGG CCACGGGGGA GGCCGAGGCA GGGGCTGGGC AGAGGGGAGA GGAAGCACAA 3061 GAAGTGGGAG TGGGAGAGGA AGCCACGTGC TGGAGAGTAG ACATCCCCCT CCTTGCCGCT 3121 GGGAGAGCCA AGGCCTATGC CACCTGCAGC GTCTGAGCGG CCGCCTGTCC TTGGTGGCCG 3181 GGGGTGGGGG CCTGCTGTGG GTCAGTGTGC CACCCTCTGC AGGGCAGCCT GTGGGAGAAG 3241 GGACAGCGGG TAAAAAGAGA AGGCAAGCTG GCAGGAGGGT GGCACTTCGT GGATGACCTC 3301 CTTAGAAAAG ACTGACCTTG ATGTCTTGAG AGCGCTGGCC TCTTCCTCCC TCCCTGCAGG 3361 GTAGGGGGCC TGAGTTGAGG GGCTTCCCTC TGCTCCACAG AAACCCTGTT TTATTGAGTT 3421 CTGAAGGTTG GAACTGCTGC CATGATTTTG GCCACTTTGC AGACCTGGGA CTTTAGGGCT 3481 AACCAGTTCT CTTTGTAAGG ACTTGTGCCT CTTGGGAGAC GTCCACCCGT TTCCAAGCCT 3541 GGGCCACTGG CATCTCTGGA GTGTGTGGGG GTCTGGGAGG CAGGTCCCGA GCCCCCTGTC 3601 CTTCCCACGG CCACTGCAGT CACCCCGTCT GCGCCGCTGT GCTGTTGTCT GCCGTGAGAG 3661 CCCAATCACT GCCTATACCC CTCATCACAC GTCACAATGT CCCGAATTCC CAGCCTCACC 3721 ACCCCTTCTC AGTAATGACC CTGGTTGGTT GCAGGAGGTA CCTACTCCAT ACTGAGGGTG 3781 AAATTAAGGG AAGGCAAAGT CCAGGCACAA GAGTGGGACC CCAGCCTCTC ACTCTCAGTT 3841 CCACTCATCC AACTGGGACC CTCACCACGA ATCTCATGAT CTGATTCGGT TCCCTGTCTC 3901 CTCCTCCCGT CACAGATGTG AGCCAGGGCA CTGCTCAGCT GTGACCCTAG GTGTTTCTGC 3961 CTTGTTGACA TGGAGAGAGC CCTTTCCCCT GAGAAGGCCT GGCCCCTTCC TGTGCTGAGC 4021 CCACAGCAGC AGGCTGGGTG TCTTGGTTGT CAGTGGTGGC ACCAGGATGG AAGGGCAAGG 4081 CACCCAGGGC AGGCCCACAG TCCCGCTGTC CCCCACTTGC ACCCTAGCTT GTAGCTGCCA 4141 ACCTCCCAGA CAGCCCAGCC CGCTGCTCAG CTCCACATGC ATAGTATCAG CCCTCCACAC 4201 CCGACAAAGG GGAACACACC CCCTTGGAAA TGGTTCTTTT CCCCCAGTCC CAGCTGGAAG 4261 CCATGCTGTC TGTTCTGCTG GAGCAGCTGA ACATATACAT AGATGTTGCC CTGCCCTCCC 4321 CATCTGCACC CTGTTGAGTT GTAGTTGGAT TTGTCTGTTT ATGCTTGGAT TCACCAGAGT 4381 GACTATGATA GTGAAAAGAA AAAAAAAAAA AAAAAAGGAC GCATGTATCT TGAAATGCTT 4441 GTAAAGAGGT TTCTAACCCA CCCTCACGAG GTGTCTCTCA CCCCCACACT GGGACTCGTG4501 TGGCCTGTGT GGTGCCACCC TGCTGGGGCC TCCCAAGTTT TGAAAGGCTT TCCTCAGCAC 4561 CTGGGACCCA ACAGAGACCA GCTTCTAGCA GCTAAGGAGG CCGTTCAGCT GTGACGAAGG 4621 CCTGAAGCAC AGGATTAGGA CTGAAGCGAT GATGTCCCCT TCCCTACTTC CCCTTGGGGC 4681 TCCCTGTGTC AGGGCACAGA CTAGGTCTTG TGGCTGGTCT GGCTTGCGGC GCGAGGATGG 4741 TTCTCTCTGG TCATAGCCCG AAGTCTCATG GCAGTCCCAA AGGAGGCTTA CAACTCCTGC 4801 ATCACAAGAA AAAGGAAGCC ACTGCCAGCT GGGGGGATCT GCAGCTCCCA GAAGCTCCGT 4861 GAGCCTCAGC CACCCCTCAG ACTGGGTTCC TCTCCAAGCT CGCCCTCTGG AGGGGCAGCG 4921 CAGCCTCCCA CCAAGGGCCC TGCGACCACA GCAGGGATTG GGATGAATTG CCTGTCCTGG 4981 ATCTGCTCTA GAGGCCCAAG CTGCCTGCCT GAGGAAGGAT GACTTGACAA GTCAGGAGAC 5041 ACTGTTCCCA AAGCCTTGAC CAGAGCACCT CAGCCCGCTG ACCTTGCACA AACTCCATCT 5101 GCTGCCATGA GAAAAGGGAA GCCGCCTTTG CAAAACATTG CTGCCTAAAG AAACTCAGCA 5161 GCCTCAGGCC CAATTCTGCC ACTTCTGGTT TGGGTACAGT TAAAGGCAAC CCTGAGGGAC 5221 TTGGCAGTAG AAATCCAGGG CCTCCCCTGG GGCTGGCAGC TTCGTGTGCA GCTAGAGCTT 5281 TACCTGAAAG GAAGTCTCTG GGCCCAGAAC TCTCCACCAA GAGCCTCCCT GCCGTTCGCT 5341 GAGTCCCAGC AATTCTCCTA AGTTGAAGGG ATCTGAGAAG GAGAAGGAAA TGTGGGGTAG 5401 ATTTGGTGGT GGTTAGAGAT ATGCCCCCCT CATTACTGCC AACAGTTTCG GCTGCATTTC 5461 TTCACGCACC TCGGTTCCTC TTCCTGAAGT TCTTGTGCCC TGCTCTTCAG CACCATGGGC 5521 CTTCTTATAC GGAAGGCTCT GGGATCTCCC CCTTGTGGGG CAGGCTCTTG GGGCCAGCCT 5581 AAGATCATGG TTTAGGGTGA TCAGTGCTGG CAGATAAATT GAAAAGGCAC GCTGGCTTGT 5641 GATCTTAAAT GAGGACAATC CCCCCAGGGC TGGGCACTCC TCCCCTCCCC TCACTTCTCC 5701 CACCTGCAGA GCCAGTGTCC TTGGGTGGGC TAGATAGGAT ATACTGTATG CCGGCTCCTT 5761 CAAGCTGCTG ACTCACTTTA TCAATAGTTC CATTTAAATT GACTTCAGTG GTGAGACTGT 5821 ATCCTGTTTG CTATTGCTTG TTGTGCTATG GGGGGAGGGG GGAGGAATGT GTAAGATAGT 5881 TAACATGGGC AAAGGGAGAT CTTGGGGTGC AGCACTTAAA CTGCCTCGTA ACCCTTTTCA 5941 TGATTTCAAC CACATTTGCT AGAGGGAGGG AGCAGCCACG GAGTTAGAGG CCCTTGGGGT 6001 TTCTCTTTTC CACTGACAGG CTTTCCCAGG CAGCTGGCTA GTTCATTCCC TCCCCAGCCA 6061 GGTGCAGGCG TAGGAATATG GACATCTGGT TGCTTTGGCC TGCTGCCCTC TTTCAGGGGT 6121 CCTAAGCCCA CAATCATGCC TCCCTAAGAC CTTGGCATCC TTCCCTCTAA GCCGTTGGCA 6181 CCTCTGTGCC ACCTCTCACA CTGGCTCCAG ACACACAGCC TGTGCTTTTG GAGCTGAGAT 6241 CACTCGCTTC ACCCTCCTCA TCTTTGTTCT CCAAGTAAAG CCACGAGGTC GGGGCGAGGG 6301 CAGAGGTGAT CACCTGCGTG TCCCATCTAC AGACCTGCAG CTTCATAAAA CTTCTGATTT 6361 CTCTTCAGCT TTGAAAAGGG TTACCCTGGG CACTGGCCTA GAGCCTCACC TCCTAATAGA 6421 CTTAGCCCCA TGAGTTTGCC ATGTTGAGCA GGACTATTTC TGGCACTTGC AAGTCCCATG 6481 ATTTCTTCGG TAATTCTGAG GGTGGGGGGA GGGACATGAA ATCATCTTAG CTTAGCTTTC 6541 TGTCTGTGAA TGTCTATATA GTGTATTGTG TGTTTTAACA AATGATTTAC ACTGACTGTT 6601 GCTGTAAAAG TGAATTTGGA AATAAAGTTA TTACTCTGAT TAAA (SEQ ID NO: 77). The corresponding amino acid sequence of human Tau protein isoform 6 can be found at NP_001116538.2: 1 MAEPRQEFEV MEDHAGTYGL GDRKDQGGYT MHQDQEGDTD AGLKESPLQT PTEDGSEEPG 61 SETSDAKSTP TAEDVTAPLV DEGAPGKQAA AQPHTEIPEG TTAEEAGIGD TPSLEDEAAG 121 HVTQEPESGK VVQEGFLREP GPPGLSHQLM SGMPGAPLLP EGPREATRQP SGTGPEDTEG 181 GRHAPELLKH QLLGDLHQEG PPLKGAGGKE RPGSKEEVDE DRDVDESSPQ DSPPSKASPA 241 QDGRPPQTAA REATSIPGFP AEGAIPLPVD FLSKVSTEIP ASEPDGPSVG RAKGQDAPLE 301 FTFHVEITPN VQKEQAHSEE HLGRAAFPGA PGEGPEARGP SLGEDTKEAD LPEPSEKQPA 361 AAPRGKPVSR VPQLKARMVS KSKDGTGSDD KKAKTSTRSS AKTLKNRPCL SPKHPTPGSS 421 DPLIQPSSPA VCPEPPSSPK YVSSVTSRTG SSGAKEMKLK GADGKTKIAT PRGAAPPGQK 481 GQANATRIPA KTPPAPKTPP SSATKQVQRR PPPAGPRSER GEPPKSGDRS GYSSPGSPGT 541 PGSRSRTPSL PTPPTREPKK VAVVRTPPKS PSSAKSRLQT APVPMPDLKN VKSKIGSTEN 601 LKHQPGGGKV QIINKKLDLS NVQSKCGSKD NIKHVPGGGS VQIVYKPVDL SKVTSKCGSL 661 GNIHHKPGGG QVEVKSEKLD FKDRVQSKIG SLDNITHVPG GGNKKIETHK LTFRENAKAK 721 TDHGAEIVYK SPVVSGDTSP RHLSNVSSTG SIDMVDSPQL ATLADEVSAS LAKQGL (SEQ ID NO: 78).The nucleotide sequence of a human MAPT transcript variant 5 (encoding 1N4R Tau) can be found at NM_001123067.4: 1 GCAGTCACCG CCACCCACCA GCTCCGGCAC CAACAGCAGC GCCGCTGCCA CCGCCCACCT 61 TCTGCCGCCG CCACCACAGC CACCTTCTCC TCCTCCGCTG TCCTCTCCCG TCCTCGCCTC 121 TGTCGACTAT CAGGTGAACT TTGAACCAGG ATGGCTGAGC CCCGCCAGGA GTTCGAAGTG 181 ATGGAAGATC ACGCTGGGAC GTACGGGTTG GGGGACAGGA AAGATCAGGG GGGCTACACC 241 ATGCACCAAG ACCAAGAGGG TGACACGGAC GCTGGCCTGA AAGAATCTCC CCTGCAGACC 301 CCCACTGAGG ACGGATCTGA GGAACCGGGC TCTGAAACCT CTGATGCTAA GAGCACTCCA 361 ACAGCGGAAG CTGAAGAAGC AGGCATTGGA GACACCCCCA GCCTGGAAGA CGAAGCTGCT 421 GGTCACGTGA CCCAAGCTCG CATGGTCAGT AAAAGCAAAG ACGGGACTGG AAGCGATGAC 481 AAAAAAGCCA AGGGGGCTGA TGGTAAAACG AAGATCGCCA CACCGCGGGG AGCAGCCCCT 541 CCAGGCCAGA AGGGCCAGGC CAACGCCACC AGGATTCCAG CAAAAACCCC GCCCGCTCCA 601 AAGACACCAC CCAGCTCTGG TGAACCTCCA AAATCAGGGG ATCGCAGCGG CTACAGCAGC 661 CCCGGCTCCC CAGGCACTCC CGGCAGCCGC TCCCGCACCC CGTCCCTTCC AACCCCACCC 721 ACCCGGGAGC CCAAGAAGGT GGCAGTGGTC CGTACTCCAC CCAAGTCGCC GTCTTCCGCC 781 AAGAGCCGCC TGCAGACAGC CCCCGTGCCC ATGCCAGACC TGAAGAATGT CAAGTCCAAG 841 ATCGGCTCCA CTGAGAACCT GAAGCACCAG CCGGGAGGCG GGAAGGTGCA GATAATTAAT 901 AAGAAGCTGG ATCTTAGCAA CGTCCAGTCC AAGTGTGGCT CAAAGGATAA TATCAAACAC 961 GTCCCGGGAG GCGGCAGTGT GCAAATAGTC TACAAACCAG TTGACCTGAG CAAGGTGACC 1021 TCCAAGTGTG GCTCATTAGG CAACATCCAT CATAAACCAG GAGGTGGCCA GGTGGAAGTA 1081 AAATCTGAGA AGCTTGACTT CAAGGACAGA GTCCAGTCGA AGATTGGGTC CCTGGACAAT 1141 ATCACCCACG TCCCTGGCGG AGGAAATAAA AAGATTGAAA CCCACAAGCT GACCTTCCGC 1201 GAGAACGCCA AAGCCAAGAC AGACCACGGG GCGGAGATCG TGTACAAGTC GCCAGTGGTG 1261 TCTGGGGACA CGTCTCCACG GCATCTCAGC AATGTCTCCT CCACCGGCAG CATCGACATG 1321 GTAGACTCGC CCCAGCTCGC CACGCTAGCT GACGAGGTGT CTGCCTCCCT GGCCAAGCAG 1381 GGTTTGTGAT CAGGCCCCTG GGGCGGTCAA TAATTGTGGA GAGGAGAGAA TGAGAGAGTG 1441 TGGAAAAAAA AAGAATAATG ACCCGGCCCC CGCCCTCTGC CCCCAGCTGC TCCTCGCAGT 1501 TCGGTTAATT GGTTAATCAC TTAACCTGCT TTTGTCACTC GGCTTTGGCT CGGGACTTCA 1561 AAATCAGTGA TGGGAGTAAG AGCAAATTTC ATCTTTCCAA ATTGATGGGT GGGCTAGTAA 1621 TAAAATATTT AAAAAAAAAC ATTCAAAAAC ATGGCCACAT CCAACATTTC CTCAGGCAAT 1681 TCCTTTTGAT TCTTTTTTCT TCCCCCTCCA TGTAGAAGAG GGAGAAGGAG AGGCTCTGAA 1741 AGCTGCTTCT GGGGGATTTC AAGGGACTGG GGGTGCCAAC CACCTCTGGC CCTGTTGTGG 1801 GGGTGTCACA GAGGCAGTGG CAGCAACAAA GGATTTGAAA CTTGGTGTGT TCGTGGAGCC 1861 ACAGGCAGAC GATGTCAACC TTGTGTGAGT GTGACGGGGG TTGGGGTGGG GCGGGAGGCC 1921 ACGGGGGAGG CCGAGGCAGG GGCTGGGCAG AGGGGAGAGG AAGCACAAGA AGTGGGAGTG 1981 GGAGAGGAAG CCACGTGCTG GAGAGTAGAC ATCCCCCTCC TTGCCGCTGG GAGAGCCAAG 2041 GCCTATGCCA CCTGCAGCGT CTGAGCGGCC GCCTGTCCTT GGTGGCCGGG GGTGGGGGCC 2101 TGCTGTGGGT CAGTGTGCCA CCCTCTGCAG GGCAGCCTGT GGGAGAAGGG ACAGCGGGTA 2161 AAAAGAGAAG GCAAGCTGGC AGGAGGGTGG CACTTCGTGG ATGACCTCCT TAGAAAAGAC 2221 TGACCTTGAT GTCTTGAGAG CGCTGGCCTC TTCCTCCCTC CCTGCAGGGT AGGGGGCCTG 2281 AGTTGAGGGG CTTCCCTCTG CTCCACAGAA ACCCTGTTTT ATTGAGTTCT GAAGGTTGGA 2341 ACTGCTGCCA TGATTTTGGC CACTTTGCAG ACCTGGGACT TTAGGGCTAA CCAGTTCTCT 2401 TTGTAAGGAC TTGTGCCTCT TGGGAGACGT CCACCCGTTT CCAAGCCTGG GCCACTGGCA 2461 TCTCTGGAGT GTGTGGGGGT CTGGGAGGCA GGTCCCGAGC CCCCTGTCCT TCCCACGGCC 2521 ACTGCAGTCA CCCCGTCTGC GCCGCTGTGC TGTTGTCTGC CGTGAGAGCC CAATCACTGC 2581 CTATACCCCT CATCACACGT CACAATGTCC CGAATTCCCA GCCTCACCAC CCCTTCTCAG 2641 TAATGACCCT GGTTGGTTGC AGGAGGTACC TACTCCATAC TGAGGGTGAA ATTAAGGGAA 2701 GGCAAAGTCC AGGCACAAGA GTGGGACCCC AGCCTCTCAC TCTCAGTTCC ACTCATCCAA 2761 CTGGGACCCT CACCACGAAT CTCATGATCT GATTCGGTTC CCTGTCTCCT CCTCCCGTCA 2821 CAGATGTGAG CCAGGGCACT GCTCAGCTGT GACCCTAGGT GTTTCTGCCT TGTTGACATG2881 GAGAGAGCCC TTTCCCCTGA GAAGGCCTGG CCCCTTCCTG TGCTGAGCCC ACAGCAGCAG 2941 GCTGGGTGTC TTGGTTGTCA GTGGTGGCAC CAGGATGGAA GGGCAAGGCA CCCAGGGCAG 3001 GCCCACAGTC CCGCTGTCCC CCACTTGCAC CCTAGCTTGT AGCTGCCAAC CTCCCAGACA 3061 GCCCAGCCCG CTGCTCAGCT CCACATGCAT AGTATCAGCC CTCCACACCC GACAAAGGGG 3121 AACACACCCC CTTGGAAATG GTTCTTTTCC CCCAGTCCCA GCTGGAAGCC ATGCTGTCTG 3181 TTCTGCTGGA GCAGCTGAAC ATATACATAG ATGTTGCCCT GCCCTCCCCA TCTGCACCCT 3241 GTTGAGTTGT AGTTGGATTT GTCTGTTTAT GCTTGGATTC ACCAGAGTGA CTATGATAGT 3301 GAAAAGAAAA AAAAAAAAAA AAAAGGACGC ATGTATCTTG AAATGCTTGT AAAGAGGTTT 3361 CTAACCCACC CTCACGAGGT GTCTCTCACC CCCACACTGG GACTCGTGTG GCCTGTGTGG 3421 TGCCACCCTG CTGGGGCCTC CCAAGTTTTG AAAGGCTTTC CTCAGCACCT GGGACCCAAC 3481 AGAGACCAGC TTCTAGCAGC TAAGGAGGCC GTTCAGCTGT GACGAAGGCC TGAAGCACAG 3541 GATTAGGACT GAAGCGATGA TGTCCCCTTC CCTACTTCCC CTTGGGGCTC CCTGTGTCAG 3601 GGCACAGACT AGGTCTTGTG GCTGGTCTGG CTTGCGGCGC GAGGATGGTT CTCTCTGGTC 3661 ATAGCCCGAA GTCTCATGGC AGTCCCAAAG GAGGCTTACA ACTCCTGCAT CACAAGAAAA 3721 AGGAAGCCAC TGCCAGCTGG GGGGATCTGC AGCTCCCAGA AGCTCCGTGA GCCTCAGCCA 3781 CCCCTCAGAC TGGGTTCCTC TCCAAGCTCG CCCTCTGGAG GGGCAGCGCA GCCTCCCACC 3841 AAGGGCCCTG CGACCACAGC AGGGATTGGG ATGAATTGCC TGTCCTGGAT CTGCTCTAGA 3901 GGCCCAAGCT GCCTGCCTGA GGAAGGATGA CTTGACAAGT CAGGAGACAC TGTTCCCAAA 3961 GCCTTGACCA GAGCACCTCA GCCCGCTGAC CTTGCACAAA CTCCATCTGC TGCCATGAGA 4021 AAAGGGAAGC CGCCTTTGCA AAACATTGCT GCCTAAAGAA ACTCAGCAGC CTCAGGCCCA 4081 ATTCTGCCAC TTCTGGTTTG GGTACAGTTA AAGGCAACCC TGAGGGACTT GGCAGTAGAA 4141 ATCCAGGGCC TCCCCTGGGG CTGGCAGCTT CGTGTGCAGC TAGAGCTTTA CCTGAAAGGA 4201 AGTCTCTGGG CCCAGAACTC TCCACCAAGA GCCTCCCTGC CGTTCGCTGA GTCCCAGCAA 4261 TTCTCCTAAG TTGAAGGGAT CTGAGAAGGA GAAGGAAATG TGGGGTAGAT TTGGTGGTGG 4321 TTAGAGATAT GCCCCCCTCA TTACTGCCAA CAGTTTCGGC TGCATTTCTT CACGCACCTC 4381 GGTTCCTCTT CCTGAAGTTC TTGTGCCCTG CTCTTCAGCA CCATGGGCCT TCTTATACGG 4441 AAGGCTCTGG GATCTCCCCC TTGTGGGGCA GGCTCTTGGG GCCAGCCTAA GATCATGGTT 4501 TAGGGTGATC AGTGCTGGCA GATAAATTGA AAAGGCACGC TGGCTTGTGA TCTTAAATGA 4561 GGACAATCCC CCCAGGGCTG GGCACTCCTC CCCTCCCCTC ACTTCTCCCA CCTGCAGAGC 4621 CAGTGTCCTT GGGTGGGCTA GATAGGATAT ACTGTATGCC GGCTCCTTCA AGCTGCTGAC 4681 TCACTTTATC AATAGTTCCA TTTAAATTGA CTTCAGTGGT GAGACTGTAT CCTGTTTGCT 4741 ATTGCTTGTT GTGCTATGGG GGGAGGGGGG AGGAATGTGT AAGATAGTTA ACATGGGCAA 4801 AGGGAGATCT TGGGGTGCAG CACTTAAACT GCCTCGTAAC CCTTTTCATG ATTTCAACCA 4861 CATTTGCTAG AGGGAGGGAG CAGCCACGGA GTTAGAGGCC CTTGGGGTTT CTCTTTTCCA 4921 CTGACAGGCT TTCCCAGGCA GCTGGCTAGT TCATTCCCTC CCCAGCCAGG TGCAGGCGTA 4981 GGAATATGGA CATCTGGTTG CTTTGGCCTG CTGCCCTCTT TCAGGGGTCC TAAGCCCACA 5041 ATCATGCCTC CCTAAGACCT TGGCATCCTT CCCTCTAAGC CGTTGGCACC TCTGTGCCAC 5101 CTCTCACACT GGCTCCAGAC ACACAGCCTG TGCTTTTGGA GCTGAGATCA CTCGCTTCAC 5161 CCTCCTCATC TTTGTTCTCC AAGTAAAGCC ACGAGGTCGG GGCGAGGGCA GAGGTGATCA 5221 CCTGCGTGTC CCATCTACAG ACCTGCAGCT TCATAAAACT TCTGATTTCT CTTCAGCTTT 5281 GAAAAGGGTT ACCCTGGGCA CTGGCCTAGA GCCTCACCTC CTAATAGACT TAGCCCCATG 5341 AGTTTGCCAT GTTGAGCAGG ACTATTTCTG GCACTTGCAA GTCCCATGAT TTCTTCGGTA 5401 ATTCTGAGGG TGGGGGGAGG GACATGAAAT CATCTTAGCT TAGCTTTCTG TCTGTGAATG 5461 TCTATATAGT GTATTGTGTG TTTTAACAAA TGATTTACAC TGACTGTTGC TGTAAAAGTG 5521 AATTTGGAAA TAAAGTTATT ACTCTGATTA AA (SEQ ID NO: 79). The corresponding amino acid sequence of human Tau protein isoform 5 can be found at NP_001116539.1: 1 MAEPRQEFEV MEDHAGTYGL GDRKDQGGYT MHQDQEGDTD AGLKESPLQT PTEDGSEEPG 61 SETSDAKSTP TAEAEEAGIG DTPSLEDEAA GHVTQARMVS KSKDGTGSDD KKAKGADGKT 121 KIATPRGAAP PGQKGQANAT RIPAKTPPAP KTPPSSGEPP KSGDRSGYSS PGSPGTPGSR 181 SRTPSLPTPP TREPKKVAVV RTPPKSPSSA KSRLQTAPVP MPDLKNVKSK IGSTENLKHQ 241 PGGGKVQIIN KKLDLSNVQS KCGSKDNIKH VPGGGSVQIV YKPVDLSKVT SKCGSLGNIH301 HKPGGGQVEV KSEKLDFKDR VQSKIGSLDN ITHVPGGGNK KIETHKLTFR ENAKAKTDHG 361 AEIVYKSPVV SGDTSPRHLS NVSSTGSIDM VDSPQLATLA DEVSASLAKQ GL (SEQ ID NO: 80). The nucleotide sequence of the human MAPT transcript variant 4 (encoding 0N3R Tau) can be found at NM_016841.5: 1 GCAGTCACCG CCACCCACCA GCTCCGGCAC CAACAGCAGC GCCGCTGCCA CCGCCCACCT 61 TCTGCCGCCG CCACCACAGC CACCTTCTCC TCCTCCGCTG TCCTCTCCCG TCCTCGCCTC 121 TGTCGACTAT CAGGTGAACT TTGAACCAGG ATGGCTGAGC CCCGCCAGGA GTTCGAAGTG 181 ATGGAAGATC ACGCTGGGAC GTACGGGTTG GGGGACAGGA AAGATCAGGG GGGCTACACC 241 ATGCACCAAG ACCAAGAGGG TGACACGGAC GCTGGCCTGA AAGCTGAAGA AGCAGGCATT 301 GGAGACACCC CCAGCCTGGA AGACGAAGCT GCTGGTCACG TGACCCAAGC TCGCATGGTC 361 AGTAAAAGCA AAGACGGGAC TGGAAGCGAT GACAAAAAAG CCAAGGGGGC TGATGGTAAA 421 ACGAAGATCG CCACACCGCG GGGAGCAGCC CCTCCAGGCC AGAAGGGCCA GGCCAACGCC 481 ACCAGGATTC CAGCAAAAAC CCCGCCCGCT CCAAAGACAC CACCCAGCTC TGGTGAACCT 541 CCAAAATCAG GGGATCGCAG CGGCTACAGC AGCCCCGGCT CCCCAGGCAC TCCCGGCAGC 601 CGCTCCCGCA CCCCGTCCCT TCCAACCCCA CCCACCCGGG AGCCCAAGAA GGTGGCAGTG 661 GTCCGTACTC CACCCAAGTC GCCGTCTTCC GCCAAGAGCC GCCTGCAGAC AGCCCCCGTG 721 CCCATGCCAG ACCTGAAGAA TGTCAAGTCC AAGATCGGCT CCACTGAGAA CCTGAAGCAC 781 CAGCCGGGAG GCGGGAAGGT GCAAATAGTC TACAAACCAG TTGACCTGAG CAAGGTGACC 841 TCCAAGTGTG GCTCATTAGG CAACATCCAT CATAAACCAG GAGGTGGCCA GGTGGAAGTA 901 AAATCTGAGA AGCTTGACTT CAAGGACAGA GTCCAGTCGA AGATTGGGTC CCTGGACAAT 961 ATCACCCACG TCCCTGGCGG AGGAAATAAA AAGATTGAAA CCCACAAGCT GACCTTCCGC 1021 GAGAACGCCA AAGCCAAGAC AGACCACGGG GCGGAGATCG TGTACAAGTC GCCAGTGGTG 1081 TCTGGGGACA CGTCTCCACG GCATCTCAGC AATGTCTCCT CCACCGGCAG CATCGACATG 1141 GTAGACTCGC CCCAGCTCGC CACGCTAGCT GACGAGGTGT CTGCCTCCCT GGCCAAGCAG 1201 GGTTTGTGAT CAGGCCCCTG GGGCGGTCAA TAATTGTGGA GAGGAGAGAA TGAGAGAGTG 1261 TGGAAAAAAA AAGAATAATG ACCCGGCCCC CGCCCTCTGC CCCCAGCTGC TCCTCGCAGT 1321 TCGGTTAATT GGTTAATCAC TTAACCTGCT TTTGTCACTC GGCTTTGGCT CGGGACTTCA 1381 AAATCAGTGA TGGGAGTAAG AGCAAATTTC ATCTTTCCAA ATTGATGGGT GGGCTAGTAA 1441 TAAAATATTT AAAAAAAAAC ATTCAAAAAC ATGGCCACAT CCAACATTTC CTCAGGCAAT 1501 TCCTTTTGAT TCTTTTTTCT TCCCCCTCCA TGTAGAAGAG GGAGAAGGAG AGGCTCTGAA 1561 AGCTGCTTCT GGGGGATTTC AAGGGACTGG GGGTGCCAAC CACCTCTGGC CCTGTTGTGG 1621 GGGTGTCACA GAGGCAGTGG CAGCAACAAA GGATTTGAAA CTTGGTGTGT TCGTGGAGCC 1681 ACAGGCAGAC GATGTCAACC TTGTGTGAGT GTGACGGGGG TTGGGGTGGG GCGGGAGGCC 1741 ACGGGGGAGG CCGAGGCAGG GGCTGGGCAG AGGGGAGAGG AAGCACAAGA AGTGGGAGTG 1801 GGAGAGGAAG CCACGTGCTG GAGAGTAGAC ATCCCCCTCC TTGCCGCTGG GAGAGCCAAG 1861 GCCTATGCCA CCTGCAGCGT CTGAGCGGCC GCCTGTCCTT GGTGGCCGGG GGTGGGGGCC 1921 TGCTGTGGGT CAGTGTGCCA CCCTCTGCAG GGCAGCCTGT GGGAGAAGGG ACAGCGGGTA 1981 AAAAGAGAAG GCAAGCTGGC AGGAGGGTGG CACTTCGTGG ATGACCTCCT TAGAAAAGAC 2041 TGACCTTGAT GTCTTGAGAG CGCTGGCCTC TTCCTCCCTC CCTGCAGGGT AGGGGGCCTG 2101 AGTTGAGGGG CTTCCCTCTG CTCCACAGAA ACCCTGTTTT ATTGAGTTCT GAAGGTTGGA 2161 ACTGCTGCCA TGATTTTGGC CACTTTGCAG ACCTGGGACT TTAGGGCTAA CCAGTTCTCT 2221 TTGTAAGGAC TTGTGCCTCT TGGGAGACGT CCACCCGTTT CCAAGCCTGG GCCACTGGCA 2281 TCTCTGGAGT GTGTGGGGGT CTGGGAGGCA GGTCCCGAGC CCCCTGTCCT TCCCACGGCC 2341 ACTGCAGTCA CCCCGTCTGC GCCGCTGTGC TGTTGTCTGC CGTGAGAGCC CAATCACTGC 2401 CTATACCCCT CATCACACGT CACAATGTCC CGAATTCCCA GCCTCACCAC CCCTTCTCAG 2461 TAATGACCCT GGTTGGTTGC AGGAGGTACC TACTCCATAC TGAGGGTGAA ATTAAGGGAA 2521 GGCAAAGTCC AGGCACAAGA GTGGGACCCC AGCCTCTCAC TCTCAGTTCC ACTCATCCAA 2581 CTGGGACCCT CACCACGAAT CTCATGATCT GATTCGGTTC CCTGTCTCCT CCTCCCGTCA 2641 CAGATGTGAG CCAGGGCACT GCTCAGCTGT GACCCTAGGT GTTTCTGCCT TGTTGACATG 2701 GAGAGAGCCC TTTCCCCTGA GAAGGCCTGG CCCCTTCCTG TGCTGAGCCC ACAGCAGCAG 2761 GCTGGGTGTC TTGGTTGTCA GTGGTGGCAC CAGGATGGAA GGGCAAGGCA CCCAGGGCAG2821 GCCCACAGTC CCGCTGTCCC CCACTTGCAC CCTAGCTTGT AGCTGCCAAC CTCCCAGACA 2881 GCCCAGCCCG CTGCTCAGCT CCACATGCAT AGTATCAGCC CTCCACACCC GACAAAGGGG 2941 AACACACCCC CTTGGAAATG GTTCTTTTCC CCCAGTCCCA GCTGGAAGCC ATGCTGTCTG 3001 TTCTGCTGGA GCAGCTGAAC ATATACATAG ATGTTGCCCT GCCCTCCCCA TCTGCACCCT 3061 GTTGAGTTGT AGTTGGATTT GTCTGTTTAT GCTTGGATTC ACCAGAGTGA CTATGATAGT 3121 GAAAAGAAAA AAAAAAAAAA AAAAGGACGC ATGTATCTTG AAATGCTTGT AAAGAGGTTT 3181 CTAACCCACC CTCACGAGGT GTCTCTCACC CCCACACTGG GACTCGTGTG GCCTGTGTGG 3241 TGCCACCCTG CTGGGGCCTC CCAAGTTTTG AAAGGCTTTC CTCAGCACCT GGGACCCAAC 3301 AGAGACCAGC TTCTAGCAGC TAAGGAGGCC GTTCAGCTGT GACGAAGGCC TGAAGCACAG 3361 GATTAGGACT GAAGCGATGA TGTCCCCTTC CCTACTTCCC CTTGGGGCTC CCTGTGTCAG 3421 GGCACAGACT AGGTCTTGTG GCTGGTCTGG CTTGCGGCGC GAGGATGGTT CTCTCTGGTC 3481 ATAGCCCGAA GTCTCATGGC AGTCCCAAAG GAGGCTTACA ACTCCTGCAT CACAAGAAAA 3541 AGGAAGCCAC TGCCAGCTGG GGGGATCTGC AGCTCCCAGA AGCTCCGTGA GCCTCAGCCA 3601 CCCCTCAGAC TGGGTTCCTC TCCAAGCTCG CCCTCTGGAG GGGCAGCGCA GCCTCCCACC 3661 AAGGGCCCTG CGACCACAGC AGGGATTGGG ATGAATTGCC TGTCCTGGAT CTGCTCTAGA 3721 GGCCCAAGCT GCCTGCCTGA GGAAGGATGA CTTGACAAGT CAGGAGACAC TGTTCCCAAA 3781 GCCTTGACCA GAGCACCTCA GCCCGCTGAC CTTGCACAAA CTCCATCTGC TGCCATGAGA 3841 AAAGGGAAGC CGCCTTTGCA AAACATTGCT GCCTAAAGAA ACTCAGCAGC CTCAGGCCCA 3901 ATTCTGCCAC TTCTGGTTTG GGTACAGTTA AAGGCAACCC TGAGGGACTT GGCAGTAGAA 3961 ATCCAGGGCC TCCCCTGGGG CTGGCAGCTT CGTGTGCAGC TAGAGCTTTA CCTGAAAGGA 4021 AGTCTCTGGG CCCAGAACTC TCCACCAAGA GCCTCCCTGC CGTTCGCTGA GTCCCAGCAA 4081 TTCTCCTAAG TTGAAGGGAT CTGAGAAGGA GAAGGAAATG TGGGGTAGAT TTGGTGGTGG 4141 TTAGAGATAT GCCCCCCTCA TTACTGCCAA CAGTTTCGGC TGCATTTCTT CACGCACCTC 4201 GGTTCCTCTT CCTGAAGTTC TTGTGCCCTG CTCTTCAGCA CCATGGGCCT TCTTATACGG 4261 AAGGCTCTGG GATCTCCCCC TTGTGGGGCA GGCTCTTGGG GCCAGCCTAA GATCATGGTT 4321 TAGGGTGATC AGTGCTGGCA GATAAATTGA AAAGGCACGC TGGCTTGTGA TCTTAAATGA 4381 GGACAATCCC CCCAGGGCTG GGCACTCCTC CCCTCCCCTC ACTTCTCCCA CCTGCAGAGC 4441 CAGTGTCCTT GGGTGGGCTA GATAGGATAT ACTGTATGCC GGCTCCTTCA AGCTGCTGAC 4501 TCACTTTATC AATAGTTCCA TTTAAATTGA CTTCAGTGGT GAGACTGTAT CCTGTTTGCT 4561 ATTGCTTGTT GTGCTATGGG GGGAGGGGGG AGGAATGTGT AAGATAGTTA ACATGGGCAA 4621 AGGGAGATCT TGGGGTGCAG CACTTAAACT GCCTCGTAAC CCTTTTCATG ATTTCAACCA 4681 CATTTGCTAG AGGGAGGGAG CAGCCACGGA GTTAGAGGCC CTTGGGGTTT CTCTTTTCCA 4741 CTGACAGGCT TTCCCAGGCA GCTGGCTAGT TCATTCCCTC CCCAGCCAGG TGCAGGCGTA 4801 GGAATATGGA CATCTGGTTG CTTTGGCCTG CTGCCCTCTT TCAGGGGTCC TAAGCCCACA 4861 ATCATGCCTC CCTAAGACCT TGGCATCCTT CCCTCTAAGC CGTTGGCACC TCTGTGCCAC 4921 CTCTCACACT GGCTCCAGAC ACACAGCCTG TGCTTTTGGA GCTGAGATCA CTCGCTTCAC 4981 CCTCCTCATC TTTGTTCTCC AAGTAAAGCC ACGAGGTCGG GGCGAGGGCA GAGGTGATCA 5041 CCTGCGTGTC CCATCTACAG ACCTGCAGCT TCATAAAACT TCTGATTTCT CTTCAGCTTT 5101 GAAAAGGGTT ACCCTGGGCA CTGGCCTAGA GCCTCACCTC CTAATAGACT TAGCCCCATG 5161 AGTTTGCCAT GTTGAGCAGG ACTATTTCTG GCACTTGCAA GTCCCATGAT TTCTTCGGTA 5221 ATTCTGAGGG TGGGGGGAGG GACATGAAAT CATCTTAGCT TAGCTTTCTG TCTGTGAATG 5281 TCTATATAGT GTATTGTGTG TTTTAACAAA TGATTTACAC TGACTGTTGC TGTAAAAGTG 5341 AATTTGGAAA TAAAGTTATT ACTCTGATTA AA (SEQ ID NO: 81). The corresponding amino acid sequence of human Tau protein isoform 4 can be found at NP_058525.1: 1 MAEPRQEFEV MEDHAGTYGL GDRKDQGGYT MHQDQEGDTD AGLKAEEAGI GDTPSLEDEA 61 AGHVTQARMV SKSKDGTGSD DKKAKGADGK TKIATPRGAA PPGQKGQANA TRIPAKTPPA 121 PKTPPSSGEP PKSGDRSGYS SPGSPGTPGS RSRTPSLPTP PTREPKKVAV VRTPPKSPSS 181 AKSRLQTAPV PMPDLKNVKS KIGSTENLKH QPGGGKVQIV YKPVDLSKVT SKCGSLGNIH 241 HKPGGGQVEV KSEKLDFKDR VQSKIGSLDN ITHVPGGGNK KIETHKLTFR ENAKAKTDHG 301 AEIVYKSPVV SGDTSPRHLS NVSSTGSIDM VDSPQLATLA DEVSASLAKQ GL (SEQ ID NO: 82).[000127] As used herein, the term “tauopathy” refers to a disease associated with abnormal tau protein expression, secretion, phosphorylation, cleavage, and / or aggregation. [000128] As used herein, “TfR” refers to a transferrin receptor protein or polypeptide, e.g., a human transferrin receptor protein or polypeptide. The amino acid sequence of the human transferrin receptor protein (hTFR) can be found at NP_001121620.1: 1 MMDQARSAFS NLFGGEPLSY TRFSLARQVD GDNSHVEMKL AVDEEENADN NTKANVTKPK 61 RCSGSICYGT IAVIVFFLIG FMIGYLGYCK GVEPKTECER LAGTESPVRE EPGEDFPAAR 121 RLYWDDLKRK LSEKLDSTDF TGTIKLLNEN SYVPREAGSQ KDENLALYVE NQFREFKLSK 181 VWRDQHFVKI QVKDSAQNSV IIVDKNGRLV YLVENPGGYV AYSKAATVTG KLVHANFGTK 241 KDFEDLYTPV NGSIVIVRAG KITFAEKVAN AESLNAIGVL IYMDQTKFPI VNAELSFFGH 301 AHLGTGDPYT PGFPSFNHTQ FPPSRSSGLP NIPVQTISRA AAEKLFGNME GDCPSDWKTD 361 STCRMVTSES KNVKLTVSNV LKEIKILNIF GVIKGFVEPD HYVVVGAQRD AWGPGAAKSG 421 VGTALLLKLA QMFSDMVLKD GFQPSRSIIF ASWSAGDFGS VGATEWLEGY LSSLHLKAFT 481 YINLDKAVLG TSNFKVSASP LLYTLIEKTM QNVKHPVTGQ FLYQDSNWAS KVEKLTLDNA 541 AFPFLAYSGI PAVSFCFCED TDYPYLGTTM DTYKELIERI PELNKVARAA AEVAGQFVIK 601 LTHDVELNLD YERYNSQLLS FVRDLNQYRA DIKEMGLSLQ WLYSARGDFF RATSRLTTDF 661 GNAEKTDRFV MKKLNDRVMR VEYHFLSPYV SPKESPFRHV FWGSGSHTLP ALLENLKLRK 721 QNNGAFNETL FRNQLALATW TIQGAANALS GDVWDIDNEF(SEQ ID NO: 85). [000129] As used herein, “treatment” or “treating” refers to all processes wherein there may be a slowing, controlling, delaying, or stopping of the progression of the disorders or disease disclosed herein, or ameliorating disorder or disease symptoms, but does not necessarily indicate a total elimination of all disorder or disease symptoms. Treatment includes administration of a protein or nucleic acid or vector or composition for treatment of a disease or condition in a patient, particularly in a human. [000130] The following examples are offered to illustrate, but not to limit, the claimed inventions. EXAMPLES Example 1: Generation and Characterization of TfR binding proteins Generation of human TfR binding proteins [000131] Antibody against human TfR was generated by immunizing AlivaMab® transgenic mice with the extracellular domains of human Transferrin Receptor 1 protein with a His tag (hTfR-ECD-6His, SEQ ID NO: 85, see Table 7) and mouse Transferrin Receptor protein (mTfR, SEQ ID NO:84). Antigen positive B-cells were sorted from pooled spleens. Binding of individual antibodies cloned from those B-cells to his-tagged hTfR-ECD was verified. [000132] Additional antibody against human TfR was generated by immunizing AlivaMab® transgenic mice with the apical domain of human Transferrin Receptor 1 proteinwith a His tag (hTfR-ApD-6His, SEQ ID NO: 86, see Table 7). Antigen positive B-cells were sorted from pooled spleens. Binding of individual antibodies cloned from those B-cells to his- tagged hTfR-ECD was verified. Table 7. Sequences of the immunogens used to generate human TfR antibodies. Immunogen Sequence SEQ ID NO mTfR-ECD-6His HHHHHHCKRVEQKEECVKLAETEETDKSETMETEDV 84IPVQTISRAAAEKLFGNMEGDCPSDWKTDSTCRMVTS ESKNVKLTVS[000133] Affinity variants of the generated human TfR antibodies were made by systematically introducing mutations into individual CDR of each antibody and the resulting variants were subjected to multiple rounds of selection with decreasing concentrations of antigen and / or increasing periods of dissociation to isolate clones with improved affinities. The sequences of individual variants were used to construct a combinatorial library which was subjected to an additional round of selection with increased stringency to identify additive or synergistic mutational pairings between the individual CDR regions. Individual combinatorial clones are sequenced. The heavy chain and light chain CDRs and VH / VL sequences of the human TfR binding domains and proteins are provided in Table 1a. [000134] Human TfR binding proteins were generated by recombinant DNA technology. Such human TfR binding proteins can be expressed in a mammalian cell line such as HEK293 or CHO, either transiently or stably transfected with an expression system using an optimal predetermined HC:LC vector ratio or a single vector system encoding both HC and LC. Clarified media, into which the protein has been secreted, can be purified using the commonly used techniques. Binding affinity [000135] Binding affinity and binding stoichiometry of the exemplified human TfR binding proteins to human and cynomolgus TfR was characterized using a surface plasmon resonance assay on a Biacore 8K instrument primed with HBS-EP+ (10mM Hepes pH7.4 + 150mM NaCl + 3mM EDTA + 0.05% (w / v) surfactant P20) running buffer and analysis temperature set at 37 °C. Target human and cynomologus TfR ECD’s were immobilized on a CM4 chip (Cytiva P / N 29104989) using standard NHS-EDC amine coupling. The TfR binding proteins were prepared at a final concentration of 0.3, 0.1, 0.033, 0.01, 0.0033, 0.001, 0.00033, 0.0001 µM respectively by dilution of stock solution into running buffer. [000136] Binding analysis was performed in a multi-cycle kinetics manner. Each analysis cycle consists of (1) injection of the lowest to highest concentration proteins over all Fc at 50 µL / min for 140 seconds followed by return to buffer flow for 400 seconds to monitordissociation phase; (2) regeneration of chip surfaces with injection of 3M magnesium chloride, for 30 seconds at 100 µL / min over all cells; and (3) equilibration of chip surfaces with a 50 µL (30-sec) injection of HBS-EP+. Data were processed using standard double-referencing and fit to a 2-state binding model using Biacore 8K Evaluation software, to determine the association rate (kon, M-1s-1units), dissociation rate (koff, s-1units), and Rmax (RU units). The equilibrium dissociation constant (KD) is calculated from the relationship KD = koff / kon, and is in molar units. Results are provided in Table 8. Table 8. Binding Affinity of Exemplified human TfR binding proteins to human or cynomolgus TfR at 37 °C Human TfR Standard error Standard error of binding Human TfR KDof the mean, Cyno TfR KDthe mean CynoBinding affinity of TfR binding proteins to human and cynomolgus TfR was also characterized by Meso Scale Discovery (MSD) using MESO QuickPlex SQ 120MM. Target human and cynomolgus TfR ECD were diluted to 1 µg / mL in 1X PBS buffer and 80 µL dispensed in 96- well MSD plate and agitated on plater shaker for ~1 min and stored at 4 °C overnight to coat the plate surface. Coated plates were washed with three times with PBS containing 0.02% Tween-20 (PBS-T), followed by addition of 200 µL of 3% blocker A to each well and agitated for 1 hour at ambient temperature. TBPs were prepared by diluting into PBS-T, starting at 2 µM top concentration and serially diluting down 1 to 3 fold. Blocked MSD plate was washed three times with 200 µL PBS-T and 80 µL serially diluted TBPs were added to each well, followed by agitation on plate shaker for 1 hour at ambient temperature. Sulfo-tag anti-human kappa chain secondary antibody (MSD, Cat. D20TF) was prepared by diluting at 1µg / mL into PBS-T buffer and 80 µL added to each well and agitated on plate shaker for 1 hour at ambient temperature. Blocked plate was washed for three times with 200 µL PBS-T. Finally, 200 µL MSD Rad Buffer T (MSD, Cat. R92TC) was added to each well and read on MSD plate reader immediately. Data was fitted to an equilibrium binding equation (see Darling and Brault, 2005, Kinetic Exclusion Assay Technology: Characterization of Molecular Interactions. Assay and Drug DevelopmentTechnologies 2: 647-657) using non-linear regression in ADT toolkit. The EC50 was calculated in molar units and results are reported in Table 9. Table 9. Binding Affinity of Exemplified human TfR binding proteins to human or cynomolgus TfR at ambient temperature by MSD Human TfR EC50 Lower- EC50 Lower- binding Upper Cl, H TfR K C TfR K Upper Cl, CynoExample 2: Synthesis and characterization of dsRNAs targeting SNCA or MAPT (e.g., siRNA) [000137] Single strands (sense and antisense) of the dsRNA duplexes were synthesized on solid support via a MerMade™ 12 (LGC Biosearch Technologies). The sequences of the sense and antisense strands were shown in Table 6a or 6b. The sense strands were synthesized using phthalamido amino C6 lcaa CPG 500 Å (Chemgenes) whereas the antisense strands used standard support (LGC Biosearch Technologies). The oligonucleotides were synthesized via phosphoramidite chemistry at either 5, 10, or 50 µmol scales. [000138] Standard reagents were used in the oligo synthesis (Table 10), where 0.1M xanthane hydride in pyridine was used as the sulfurization reagent and 20% DEA in ACN was used as an auxiliary wash post synthesis. All monomers (Table 11) were made at 0.1M in ACN and contained a molecular sieves trap bag. [000139] The oligonucleotides were cleaved and deprotected (C / D) at 45 °C for 20 hours. The sense strands were C / D from the CPG using cold 50% (methylamine / ammonia hydroxide 28-30%) at ambient temperature for 3 hrs, whereas 3% DEA in ammonia hydroxide (28-30%, cold) was used for the antisense strands. C / D was determined complete by IP-RP LCMS when the resulting mass data confirmed the identity of sequence. Dependent on scale, the CPG was filtered via 0.45 um PVDF syringeless filter, 0.22 um PVDF Steriflip® vacuum filtration or 0.22um PVDF Stericup® Quick release. The CPG was back washed / rinsed with either 30% EtOH / RNAse free water then filtered through the same filtering device and combined with the first filtrate. This was repeated twice. The material was then divided evenly into 50 mL falcon tubes to remove organics via Genevac™. After concentration, the crude oligonucleotides were diluted back to synthesized scale with RNAse free water and filtered either by 0.45 µm PVDF syringeless filter, 0.22 µm PVDF Steriflip® vacuum filtration or 0.22 µm PVDF Stericup® Quick release. [000140] The crude oligonucleotides were purified via AKTA™ Pure purification system using anion-exchange (AEX). For AEX, an ES Industry Source™ 15Q column maintaining column temperature at 65 °C with MPA: 20mM NaH2PO4, 15% ACN, pH 7.4 and MPB: 20 mM NaH2PO4, 1M NaBr, 15% ACN, pH 7.4. Fractions which contained a mass purity greater than 85% without impurities >5% where combined. [000141] The purified oligonucleotides were desalted using 15 mL 3K MWCO centrifugal spin tubes at 3500xg for ~30 min. The oligonucleotides were rinsed with RNAse free water until the eluent conductivity reached < 100 usemi / cm. After desalting was complete, 2-3 mL of RNAse free water was added then aspirated 10x, the retainment was transferred to a 50 mL falcon tube, this was repeated until complete transfer of oligo by measuring concentration of compound on filter via nanodrop. The final oligonucleotide was then nano filtered 2x via 15 mL 100K MWCO centrifugal spin tubes at 3500xg for 2 min. The final desalted oligonucleotides were analyzed for concentration (nano drop at A260), characterized by IP-RP LC / MS for mass purity (Table 9) and UPLC for UV-purity. Table 9: Exemplary LC / MS data dsRNA MW MW15S: SEQ ID NO 517318.95 7319.2AS: SEQ ID NO 467825.19 7826.3Table 10 Oligonucleotide Synthesis Reagents ReagentsDeblock Solution, 3% TCA in DCM (w / v)Table 11 Phosphoramidites Phosphoramidite Abbreviation Supplier Catalog # CAS 1U3'CE phosphoroamiditep g p g [000142] Certain abbreviations are defined as follows: “ACN” refers to acetonitrile; “aAEX” refers to analytical anion exchange; “AS” refers to antisense strand; “DAR” refers to drug / siRNA to antibody / protein ratio; “DCM” refers to dichloromethane; “DHAA” refers to dehydroascorbic acid; “DIEA” refers to N,N-diisopropylethylamine; “DMF” refers to dimethylformamide; “dsRNA” refers to double stranded ribonucleic acid; “DTT” refers to dithiothreitol; “EtOAc” refers to ethyl acetate; “FEP” refers to fluorinated ethylene propylene; “FMI” refers to Fluid Metering Inc; “h” refers to hours; “HATU” refers to hexafluorophosphate azabenzotriazole tetramethyl uranium; “HPLC” refers to high-performance liquid chromatography; “LC / MS” refers to liquid chromatography mass spectrometry; “LTQ / MS” refers to linear ion trap mass spectrometer; “min” refers to minutes; “MTBE” refers to methyl tert-butyl ether; “MW” refers to molecular weight; “NHS” refers to N-hydroxysuccinimide; “OD” refers to optical density; “PBS” phosphate-buffered saline; “PEG” refers to polyethylene glycol; “rpm” refers to revolutions per minute; “SEC” refers to size exclusion chromatography; “siRNA” refers to small interfering RNA; “SMCC” refers to succinimidyl-4-(N- maleimidomethyl)cyclohexane-1-carboxylate; “SS” refers to sense strand; “TCO” refers to trans- cyclo-octene; “TEA” refers to triethylamine; “TFA” refers to trifluoroacetic acid; “TfR” refers to transferrin receptor; “THF” refers to tetrahydrofuran; “TRIS” refers to tris(hydroxymethyl)aminomethane; and “UV” refers to ultraviolet.Scheme 1 asolvent such as acetic acid followed by treatment with acetic anhydride and sodium acetate in a solvent such as toluene to give compound (2). Step B shows the acidic deprotection of compound (2) with an acid such as TFA in a suitable solvent such as DCM followed by an amide coupling with methyltetrazine-PEG4-acid using an amide coupling reagent such as HATU with an appropriate base such as N,N-diisopropyl amine in a solvent system such as DMF and THF to give compound (3). One skilled in the art will recognize that a variety of coupling reagents, bases, and solvents can be used to perform an amide coupling. Scheme 2[000144] Scheme 2, step A depicts the transformation of a cis-olefin compound (4) to the trans olefin compounds (5) and (6) through using a closed-loop flow apparatus using irradiation and capture on a column of silver nitrate absorbed onto silica gel. Step B shows the reaction of compound (5) with N,N’-disuccinimidyl carbonate using a suitable base such as TEA in a solvent such as ACN to give compound (7). Scheme 3Step A[000145] a one anhydride using an appropriate base such as DIEA in a solvent such as THF followed by an amide coupling with N-hydroxysuccinimide using an appropriate coupling reagent such as 1-(3- dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride with an appropriate base such as 4- dimethylaminopyridine to give compound (9). One skilled in the art will recognize that a variety of coupling reagents, bases, and solvents can be used to perform an amide coupling. Scheme 4a solvent such as acetic acid followed by treatment with TEA in a solvent such as toluene to give compound (11). Step B depicts the conversion of compound (11) to compound (12) in a manner essentially analogous to scheme 1, step B. Preparation 1 tert-Butyl 4-[2-(2,5-dioxopyrrol-1-yl)ethyl]piperazine-1-carboxylate[000147] tert-Butyl 4-(2-aminoethyl)piperazine-1-carboxylate (3.00 g, 13.1 mmol) was dissolved in acetic acid (6 mL). Added furan-2,5-dione (1.28 g, 13.1 mmol) and stirred at ambient temperature for 7 h. The mixture was then stored in a refrigerator for 18 h. Removed most of the acetic acid under vacuum at 50 °C. Added acetic anhydride (10 mL, 106 mmol) and sodium acetate (1.6 g, 20 mmol) then heated to 80 °C for 2 h. Added toluene and removed most of the acetic anhydride under vacuum. The mixture was taken into saturated aqueous ammonium chloride (60 mL) and extracted with DCM (3 × 50 mL). The combined organic layers were dried over anhydrous sodium sulfate, filtered, and concentrated under vacuum to give the crude product as a dark oil. Purified via silica gel chromatography eluting with EtOAc / hexane to give the title compound (2.1 g, 52%). LC / MS m / z 310.3 (M+H). Preparation 2 tert-Butyl 4-[3-(2,5-dioxopyrrol-1-yl)propyl]piperazine-1-carboxylate [000148] Furan-2,5-dioneto a solution of tert-butyl 4-(3- aminopropyl)piperazine-1-carboxylate (2.00 g, 7.97 mmol) in acetic acid (8 mL, 140 mmol). The mixture was stirred at ambient temperature for 12 hours then concentrated under vacuum to give the crude intermediate (Z)-4-[3-(4-tert-butoxycarbonylpiperazin-1-yl)propylamino]-4-oxo-but-2- enoic acid (2.72 g, 7.97 mmol) which was then dissolved in toluene (80 mL). TEA (5.6 mL, 40 mmol) and 4Å molecular sieves (8.8 g) were added. The flask was equipped with a Dean- Stark trap, and the mixture was heated at 120 °C for 48 hours. After cooling to ambient temperaure, the solids were removed by filtration, and washed with DCM (40 mL). The volatiles were removed under reduced pressure to give a residue that was dried under vacuum. The thick residue was purified by normal phase chromatography eluting with (10% MeOH / MTBE) / DCM to give the title compound as a yellow, flaky powder (353 mg, 13.7%). LC / MS m / z 324 (M+H).Preparation 3 1-[2-[4-[3-[2-[2-[2-[2-[4-(6-Methyl-1,2,4,5-tetrazin-3- yl)phenoxy]ethoxy]ethoxy]ethoxy]ethoxy]propanoyl]piperazin-1-yl]ethyl]pyrrole-2,5-dione [000149](150 mg, 0.485 mmol) was dissolved in DCM (2 mL). Added TFA (1 mL, 13 mmol) and stirred at ambient temperature for 1 h. Concentrated under vacuum and further dried under high vacuum for 18 h to give the intermediate 1-(2-piperazin-1-ylethyl)pyrrole-2,5-dione trifluoroacetate. This material and methyltetrazine-PEG4-acid (130 mg, 0.283 mmol) were dissolved in DMF (2.0 mL) and THF (2 mL). HATU (380 mg, 0.969 mmol) was then added followed by N,N-diisopropylamine (0.45 mL, 2.6 mmol). Stirred at ambient temperature for 2 h. Diluted with DCM (50 mL) and washed with saturated aqueous ammonium chloride (30 mL). The organic layer was dried over anhydrous sodium sulfate, filtered, and concentrated under vacuum to give crude product as a red solid. Purified via silica gel chromatography eluting with 0-20% MeOH / EtOAc to give the title compound as a red solid (150 mg, 49%). LC / MS m / z 628.6 (M+H).Preparation 4 1-[3-[4-[3-[2-[2-[2-[2-[4-(6-Methyl-1,2,4,5-tetrazin-3- yl)phenoxy]ethoxy]ethoxy]ethoxy]ethoxy]propanoyl]piperazin-1-yl]propyl]pyrrole-2,5-dione [000150] 1-yl)propyl]piperazine-1-carboxylate in a manner essentially analogous to the methods found in Preparation 3. LC / MS m / z 642 (M+H). Preparation 5 (1R,4E)-Cyclooct-4-en-1-ol (axial) and (1R,4E)-cyclooct-4-en-1-ol (equatorial)[000151] A closed-loop, flow was that permitted irradiation of a solution of cis-olefin and cycling of said solution through a silver nitrate-absorbed onto silica gel cartridge. Only the trans-olefin is retained in the silica gel, thus the cis olefin is recycled back to irradiation stage. [000152] Equipment: (A) UV Lamp (Pen-Ray 099912-1, 254 nM), power supply 99-0055- 01 Lamp Current 18 mA / AC. Per manufacturer’s description, this lamp produces between 4400 and 4750 microwatts / cm^2 intensity at 0.75" for 254 nM light. (B) FMI pump set to 10 mL / min that draws the reaction mixture from a Pyrex® round bottom flask (250 mL). This was connected to FEP 1 / 16" tubing that was wrapped around a cold finger (total 7 mL loop, air cooling). The UV lamp was placed in the center of the cold finger to irradiate the sample with air cooling. After the irradiation, the sample tubing continued into an ISCO SLM that contained 25 g ofsilver nitrate impregnated silica gel (See Fox, et.al., Angewandte Chemie, International Edition Engl 2009, 48(38), 7013-7016; Synthesis 2018, 50, 4875). [000153] The following steps were performed. Loaded a 50 g silica gel cartridge with 25 g of silver nitrate absorbed onto silica gel on top, covered in aluminum foil, and conditioned by pumping the 1:1 hexanes / diethyl ether solvent mixture for 1 h. Mixed (4Z)-cyclooct-4-en-1-ol; racemic at hydroxyl position (2.00 g, 15.8 mmol) and methyl benzoate (2.0 mL, 16 mmol) in n- hexane (220 mL) and diethyl ether (220 mL), turned on the UV lamp, and circulated the solution through the coil around the cold finger through the silica gel / silver nitrate cartridge and back through the system at a flow rate of 10mL / min for 96 h. Flushed the silica cartridge with EtOAc (200 mL) and dried with air. Discarded the filtrate. Rinsed the dried silica cartridge with concentrated NH4OH (150 mL) followed by DCM (150 mL). Separated the layers and extracted the aqueous with DCM (2 × 50mL). Washed the combined organic layers with saturated aqueous sodium chloride, dried over MgSO4, filtered, and concentrated under reduced pressure. Purified via silica gel chromatography eluting with 0-45% MTBE / hexane to give the two products as clear liquids. Axial - (1R,4E)-cyclooct-4-en-1-ol (569.8 mg, 28.5%).1H NMR (CDCl3) 5.63-5.55 (m, 1H), 5.44-5.36 (m, 1H), 3.50-3.45 (m, 1H), 2.39-2.32 (m, 3H),1.94 (m, 4H), 1.73-1.66 (m, 3H). Equatorial - (1R,4E)-cyclooct-4-en-1-ol (673.6 mg, 33.7%).1H NMR (CDCl3): 5.60- 5.57 (m, 2H), 4.05 (dd, J= 5.3, 10.2 Hz, 1H), 2.44-2.37 (m, 1H), 2.29-2.22 (m, 2H), 2.18-2.13 (m, 2H), 1.93-1.86 (m, 4H), 1.32-1.25 (m, 1H). Preparation 6 [(1R,4E)-Cyclooct-4-en-1-yl] (2,5-dioxopyrrolidin-1-yl) carbonate [000154] N,N’-disuccinimidylmmol) in small portions (~250-300 mg each addition, five minutes apart) was added to a mixture of 1R,4E)-cyclooct-4-en-1-ol (axial) (569 mg, 4.50 mmol) and TEA (2.5 mL, 18 mmol) in ACN (25 mL). The mixture was covered in aluminum foil and stirred at ambient temperature for 60 h. Solvent was removed under reduced pressure to give an oil that was partitioned between water (20 mL) and diethylether (50 mL). The layers were separated and the aqueous was extracted with diethyl ether (2 × 50 mL). The organic layers were combined and washed with saturated ammonium chloride, then with saturated aqueous sodium chloride, dried over MgSO4, filtered, and concentrated under reduced pressure. Silica gel chromatography was used to purify and eluted with 0-60% MTBE / hexanes to give the title compound as a colorless residue that formed a white solid (732 mg, 61%). LC / MS m / z 324 (M+H). Preparation 7 (2,5-Dioxopyrrolidin-1-yl) 4-[[2-methyl-2-(2-pyridyldisulfanyl)propyl]amino]-4-oxo-butanoate [000155] 2-Methyl-2-(245 mg, 0.976 mmol), glutaric anhydride (112 mg, 0.972 mmol), and DIEA (360 μL, 2.16 mmol) were added together in THF (4 mL) and heated at 45 ºC for 12 h with vigorous stirring. After this time, the mixture was cooled to ambient temperature and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (224 mg, 1.17 mmol) and 4-dimethylaminopyridine (25 mg, 0.20 mmol) were added. The mixture was stirred at ambient temperature for 5 min before adding add N- hydroxysuccinimide (126 mg, 1.07 mmol) in one portion followed by stirring for 36 h. The mixture was filtered, and the resulting filtrate was loaded directly onto silica gel (2 g). Silica gel chromatography was used to purify and eluted with 75% EtOAc / hexanes to give the title compound as a light, cloudy residue (100.2 mg, 24%). LC / MS m / z 426 (M+H) (Hydrolyzed NHS ester). TCO-Functionalization SNCA [000156] In a set of 4 × 50 mL Falcon™ tubes, the sense strand of the SNCA dsRNA with a hexylamine chain attached at the 3’ end (SNCA_SS-3C6A) (measured concentration of SS calculated to be OD / mL of 412.5 or 2mM, 120 mL, 0.24 mmol) and 20X borate buffer (6 mL) were equally divided (10 mL each) and each were treated with 7.5 mL of a solution of [(1R,4E)- cyclooct-4-en-1-yl] (2,5-dioxopyrrolidin-1-yl) carbonate (1.65 g, 6.17 mmol) dissolved in 1,4- dioxane (100 mL). Mixed at 25 °C at 600 rpm for 30 min. The remainder of the SS sample wasdivided and reacted in the same way to yield a total of 12 sample vessels, each containing ~150 mg of crude SS starting material. The dioxane was removed by placing the Falcon™ tubes on a Genevac evaporator. The remaining aqueous solutions were combined and filtered to remove any suspended solids. Purified on an AKTA™ pure chromatography system using 13-45% ACN in 50mM NaOAc (aq) with a flow rate = 40mL / min. Combined the appropriate fractions, and removed the organics on a SpeedVac™ before desalting and concentrating to yield 214 mL which measured OD / mL of 127.3 equating to 624µM and a total of 973 mg. LTQ / MS m / z 7292; UV purity 99+%. TCO-SNCA Duplex [000157] The nanodrop concentrations for the aqueous solutions of each strand (average of 5x) were measured as SS = 624µM, and AS = 1094µM. Mixed 210 mL of SS and 113.7 mL of AS, then shook at ambient temperature for 30 min. The amount of residual SS strand was measured until completion and required adding an additional 21.9 mL of AS. The resulting 345 mL of the solution measured (Nanodrop™ Lite, 6x average, 20x dilution) OD / mL of 159.5 equating to 421µM and a total of 2.19 g. LTQ / MS m / z 7291,7825; UV purity >99%. SMCC-functionalization of SNCA dsRNA [000158] A freshly prepared solution of (2,5-dioxopyrrolidin-1-yl) 4-[(2,5-dioxopyrrol-1- yl)methyl]cyclohexanecarboxylate (185 mg, 0.542 mmol) in THF (50 mL) was added to SNCA_SS-3C6A (44 mL, 0.0528 mmol; OD / mL of 250.4, or ~1200 µM (~8.8 mg / mL)) in 0.2M phosphate buffer (44 mL). Vortexed vigorously for 2 minutes, and then shook at ambient temperature at 900 rpm for 2 h total. Analysis by LTQ showed about 94-95% conversion. Acidified to pH~4 with 20-30 drops of 5N HCl, and then removed organics in a Genevac concentrator. Desalted by centrifugal filtration on a 3K spin filter (4 × 4000 rpm, 30 min), and pooled the retentates. The OD measurement of the solution (average of 3 measurements, 10x dilution) was 266 equating to 1.3mM and a total of 316 mg. Extinction coefficient was 204.12. LTQ / MS m / z 7358.SMCC-SNCA Duplex [000159] The nanodrop concentrations of aqueous solutions of each strand (average of 3x) were measure as SS = 1322µM and AS = 1108µM. Mixed 32 mL of SS and 36.2 mL of AS and shook for 30 min at 30 °C. The amount of residual SS strand was measured until completion and required adding an additional 360 µL of AS. Removed endotoxins by filtering through a 0.45 µM filter. The resulting 75 mL of solution measured (Nanodrop™ Lite, 5x average, 10x dilution) 217 OD / mL equating to 575µM and a total of 653 mg. LTQ / MS m / z 7358,7825; UV purity 99+%. GDM-Functionalization SNCA [000160] In a 15 mL Falcon™ tube, diluted SNCA_SS-3C6A (measured concentration of SS calculated to be OD / mL of 247.6 or 1.21mM, 3 mL, 0.0036 mmol) with 20X borate buffer (0.3 mL) and water (3 mL, 166.530 mmol) then added (2,5-dioxopyrrolidin-1-yl) 5-[[2-methyl-2- (2-pyridyldisulfanyl)propyl]amino]-5-oxo-pentanoate (3.6 mL, 0.75M in dioxane). Mixed at 200 rpm for 1 h. The organics were removed on a SpeedVac™, desalted, and concentrated three times with water to give SNCA_SS-3C6A-GDM with a total yield of 13.2mL (OD / mL of 35.88, equating to 175.8µM and a total of 17.3 mg). Extinction coefficient was 204.12. LTQ1 MS m / z 7449 (UV purity 95+%). [000161] Added 2 tris(2-carboxyethyl)phosphine hydrochloride (75 µL of 100mM solution in water) to SNCA_SS-3C6A-GDM. Shook at 10 °C for 4 h, and then 16 h at ambient temperature. Added additional tris(2-carboxyethyl)phosphine hydrochloride (75 µL of 100mM solution in water), and shook for an additional 16 hours. Desalted by centrifugal filtration on a 3K spin filter (3 × 40 min, 4000 rpm), and pooled the retentates to give 10 mL. The OD measurement of the solution (average of 4 measurements, 10x dilution) was 63.6 equating to 311.4µM and a total of 22.9 mg. Extinction coefficient was 204.12. LTQ / MS m / z 7340; UV purity 99+%. GDM Annealing Step [000162] The nanodrop concentrations of aqueous solutions of each strand (average of 4x) are SS = 311.4µM and AS = 431.3µM. Mixed 10 mL of SS and 6.7 mL of AS with 5 mL of water and shook for 30 min. The amount of residual SS strand was measured until completionand required adding an additional 560 µL of AS. Concentrated on 3K MW-cut off filter (20 min), then 50k spin filtration, and further concentrated through a 3K filter. The resulting 6 mL of solution measured (Nanodrop™ Lite, 5x average, 20x dilution) 181.62 OD / mL equating to 486 µM and a total of 44.2 mg. LTQ / MS m / z 7340,7825; UV purity 99+%. MAPT dsRNA functionalization and anneal can be performed in the same way as SNCA dsRNA described above. Conjugation of dsRNA to TfR binding proteins [000163] Site-specific native or engineered cysteine amino acid residues in the TfR binding proteins were used to conjugate dsRNA. Cysteines can be engineered into the primary amino acid sequence of the TfR binding proteins. The approach of introducing cysteines as a means for conjugation has been described in WO 2018 / 232088, which is both incorporated by reference in its entirety and incorporated specifically in relation to conjugation via cysteine residues. For engineered cysteine conjugation, the TfR binding proteins were first reduced with 40 molar equivalents reducing agent dithiothreitol (DTT) at 37 °C for two hours, followed by desalting to remove reducing agent via dialysis or desalting columns. This is followed by re-oxidation of the TfR binding protein to reform the structural disulfides with 10 molar equivalent dehydroascorbic acid (DHAA) incubation at ambient temperature for two hours. A follow up desalting was performed to remove oxidizing agent. [000164] Conjugation of dsRNA onto TfR binding proteins were done using the following methods. Conjugation Scheme 1 [000165] In the first method, a bifunctional maleimide-methyl-tetrazine linker was conjugated to the engineered cysteine of the TfR binding proteins at neutral pH by addition of the linker to the TfR binding protein at 20 molar equivalents and incubating at ambient temperature for 1 h. Following which, a desalting step was performed to remove excess linker. Then, trans-cyclo-octene (TCO) functionalized dsRNA was added onto the protein linker at 4 molar equivalents for overnight conjugation at 4 °C. Step 1a: TfR binding protein conjugation with maleimide-methyl-tetrazine linkerring opening NNO O[000166] The second conjugation method utilized the SMCC-functionalized dsRNA for conjugating onto the engineered cysteine of the TfR binding proteins. For this method, TfR binding protein was prepared similarly as above to make the engineered thiol available for conjugation by undergoing a reduction and oxidation process of the TfR binding proteins. This is followed by incubating the SMCC-dsRNA with the TfR binding proteins at 4 molar equivalents for overnight conjugation at 4 °C. [000167] Optionally, following conjugation a maleimide hydrolysis step can be done to secure the linker-payload in terminal stage and avoid deconjugation during human body circulation via retro-Michael addition. This succinimide ring hydrolysis process was done byelevating the conjugate pH to 9.0 using 50mM Arginine (stock solution of 0.7M arginine, pH 9.0 was used) and incubating the solution at 37 °C for 20 hours. The hydrolysis state of the maleimide was confirmed by LCMS characterization of +18Da that is incurred by the water addition to the succinimide ring. Step 1a: TfR binding protein conjugation with SMCC linker O O O O -P N +Conjugation Scheme 3 [000168] The third conjugation method utilized GDM-functionalized dsRNA for conjugating onto the engineered cysteine of the TfR binding protein via disulfide bond. For this method, TfR binding protein was prepared similarly as above to make the engineered thiol available for conjugation by undergoing reduction and oxidation process of the TfR binding protein. Then, dithiobis(5-nitropyridine) was added in as 20 molar equivalents to the protein to generate the intermediate prior to dsRNA conjugation. Excess dithiobis(5-nitropyridine) was removed by desalting. In a second step, GDM-functionalized dsRNA was added to the protein intermediate in a 4 molar equivalents. The dithiobis(5-nitropyridine) acts as a leaving group in this reaction and replaced by the GDM-dsRNA. Step 1: TfR binding protein conjugation with dithiobis(5-nitropyridine) for intermediate generation[000169] Conjugation was monitored using analytical anion exchange chromatography. A ProPac™ SAX-10 HPLC Column, 10µm particle, 4mm diameter, 250mm length was utilizedwith the following method. Flow rate of 1 mL / min, Buffer A: 20mM TRIS pH 7.0, Buffer B: 20 mM TRIS pH 7.0 + 1.5M NaCl, at 30 ºC. Table 12: HPLC gradient used to assess dsRNA conjugation to TfR binding protein Time [min] A B [%][000170] Drug / siRNA to antibody / protein ratio (DAR) was calculated based on peak area % from the analytical anion exchange (aAEX) chromatogram. [000171] Post conjugation of dsRNA to the TfR binding protein, excess dsRNA and unconjugated protein was removed by further purification. Either preparative size exclusion chromatography (SEC) or preparative anion exchange chromatography was utilized for purification of the final conjugate. Preparative SEC was performed using Cytiva Superdex® 200 in 1X PBS pH 7.2 under an isocratic condition. Alternatively, anion exchange, e.g., ThermoFisher POROSTMXQ, was used with starting buffer of 20mM TRIS pH 7.0 and eluting with 20 column volume gradient with a buffer containing 20mM TRIS pH 7.0 and 1M NaCl. These resulted in purified TfR binding protein-dsRNA conjugate devoid of excess dsRNA and minimal unconjugated protein. The resulting conjugate profile was analyzed by analytical anion exchange for final DAR quantitation (see Figures 1A-1E; and Table 13).Table 13. siRNA / drug to TBP / antibody ratio (DAR) Average DAR % of DAR0 % of DAR1 % of DAR2 TBP3- dsRNA 1.03 0.90 95.19 3.64Example 4: In vivo characterization of the human TfR binding proteins-dsRNA conjugates [000172] Pharmacodynamic properties of human TfR binding protein-MAPT dsRNA conjugates were assessed in NHPs according to the following. Cynomolgus monkeys weighing 2-3 kg were dosed intravenously in the thigh with i) PBS (n=5), ii) TBP2-dsRNA No. 26 (n=5) at 20 mg / kg effective siRNA concentration, or iii) TBP3-dsRNA No. 26 (n=5) at 20 mg / kg effective siRNA concentration and sacrificed 29 days after the first dose. Deeply anesthetized animals underwent cardiac perfusion, then brain, spinal cord and peripheral tissues were collected. The brain was coronally sectioned, 3mm punches were collected from indicated subregions and frozen, as well as tissues were collected from spinal cord, liver, and muscles to assess target mRNA levels by RT-qPCR in tissue homogenates. The total RNA from NHP tissues were isolated using the RNadvance Tissue kit (Beckman Coulter, Indianapolis, IN) manually or on a Biomek i7 liquid handler (Beckman Coulter), following the manufacturer’s procedure with some modifications. In brief, the frozen tissue sections were mixed with one 5mm stainless steel ball, lysis buffer and proteinase K, homogenized for 5 cycles of 30s at 1200rpm, with an interval of 20s between cycles, on a 2010 GenoGrinder (SPEX SamplePrep, Metuchen, NJ). Tissues from some regions were shaved on dry ice, prior to homogenization. The homogenates were incubated at 37 °C for 1 hour, then extracted with an equal volume of phenol- chloroform. The RNA in the supernatant were purified with the RNadvance tissue kit, where a 30 minute digestion with DNase was included. The concentration and the purity (A260 / A280) of the RNA elute were determined by spectrophotometry. RNA was normalized to 15ng / 10uL PCR, digested again with ezDNase (ds-DNA specific) prior to reverse-transcription using the SSIVVILO kit (Thermo Fisher Scientific, Waltham, MA). The expression of the respective gene targets in the cDNA was determined using TaqMan qPCR assays on the QuantStudio 7 Pro platform (Thermo Fisher Scientific). Gene expression levels of the MAPT were normalized by GAPDH using respective probes (ThermoFisher). [000173] Peripheral IV administration of TBP2-dsRNA No. 26 at 20 mg / kg in NHPs led to reduction of MAPT mRNA in key brain regions compared to PBS treatment group at 29 days following dosing. As shown in Figure 2A, MAPT mRNA reductions were demonstrated in the hippocampus (H, 31%), temporal cortex (TCTX, 28%), parietal cortex (PCTX, 23%), motor cortex (MCTX, 26%) and prefrontal cortex (PFC, 26%). [000174] Peripheral IV administration of TBP3- dsRNA No. 26 at 20 mg / kg dose in NHPs also led to reduction of MAPT mRNA in key brain regions compared to PBS treatment group at 29 days following dosing. As shown in Figure 2B, MAPT mRNA reductions were demonstrated in the hippocampus (42%), temporal cortex (41%), parietal cortex (37%), motor cortex (32%) and prefrontal cortex (36%). Example 5. Further characterization of the human TfR binding proteins-dsRNA conjugates in human TfR (hTfR) transgenic mice [000175] The pharmacodynamic efficacy of the human TfR binding proteins-dsRNA conjugates were evaluated in human transferrin transgenic mice at various doses of siRNA concentrations. TBP2-SNCA dsRNA No. 13 or TBP3-SNCA dsRNA No. 13 conjugates were dosed in hTfR transgenic mice by a single IV injection at 5 mg / kg, 0.5 mg / kg or 0.1 mg / kg of siRNA concentration and compared to PBS dosed group (n=5 or 3 each group). For takedowns, deeply anesthetized animals underwent cardiac perfusion 28 days following IV dosing, then brain tissues were collected and processed for RT-qPCR in tissue homogenates. [000176] As shown in Figure 3, TBP2-SNCA dsRNA No. 13 and TBP3-SNCA dsRNA No. 13 conjugate demonstrated significant reduction of SNCA mRNA in brain compared to the PBS treated group. The SNCA mRNA reduction level was similar in each dose group treated by either TBP2-SNCA dsRNA No. 13 or TBP3-SNCA dsRNA No. 13 conjugate (Figure 3). Specifically, for TBP2-SNCA dsRNA No. 13 conjugate, 5 mg / kg siRNA dose treatment resulted in 10% SNCA mRNA remaining (90% knock down), 0.5 mg / kg siRNA dose treatment resulted in 20% SNCA mRNA remaining (80% knock down), 0.1 mg / kg siRNA dose treatment resulted in 39%SNCA mRNA remaining (61% knock down). For TBP3-SNCA dsRNA No. 13 conjugate, 5 mg / kg siRNA dose treatment resulted in 11% SNCA mRNA remaining (89% knock down), 0.5 mg / kg siRNA dose treatment resulted in 21% SNCA mRNA remaining (79% knock down), 0.1 mg / kg siRNA dose treatment resulted in 48% SNCA mRNA remaining (52% knock down). Example 6. Further characterization of the mouse TfR binding proteins-dsRNA conjugates in human Tau (hTau) transgenic mice [000177] The pharmacodynamic efficacy of the mouse TfR binding proteins-dsRNA conjugates were evaluated in human tau (hTau) transgenic mice at various doses of siRNA concentrations. mTBP2-MAPT dsRNA No. 26 were dosed in hTau transgenic mice by a single IV injection at 100 mg / kg, 10 mg / kg or 1 mg / kg of siRNA concentration and compared to PBS dosed group (n=5 or 3 each group). For takedowns, deeply anesthetized animals underwent cardiac perfusion 28 days following IV dosing, then brain tissues were collected and processed for RT-qPCR in tissue homogenates. [000178] As shown in Figure 4, mTBP2-MAPT dsRNA No. 26 demonstrated significant reduction of MAPT mRNA in brain compared to the PBS treated group. Specifically, for mTBP2-MAPT dsRNA No. 26 conjugate, 100 mg / kg siRNA dose treatment resulted in 39% MAPT mRNA remaining (61% knock down), 10 mg / kg siRNA dose treatment resulted in 60% MAPT mRNA remaining (40% knock down), 1 mg / kg siRNA dose treatment resulted in 85% MAPT mRNA remaining (15% knock down).SEQUENCE LISTING SEQ Sequence ID NO I V I V V F L I P H Q S SI G I P H Q S SI GCIYSTSGGRTYYASWVKG GDDSISDAYFDL SS SVYNNNRLA A T A A T SI NmU*fG*mGmAfAmCmUfGmAmGmCmAmCfUmUfGmUmAmCmAmG*mG*mA mU*fG*fGmAmAmCfUmGmAmGmCmAmCfUmUfGmUmAmCmAmG*mG*mA * * * * G G T G T A A T G A C A G T G1261 CATGCTTATA AGCAACATGA ATTAAGAACT GACACAAAGG ACAAAAATAT AAAGTTATTA 1321 ATAGCCATTT GAAGAAGGAG GAATTTTAGA AGAGGTAGAG AAAATGGAAC2941 TTCTCCCAAG TTATTCAGCC TCATATGACT CCACGGTCGG CTTTACCAAA ACAGTTCAGA 3001 GTGCACTTTG GCACACAATT GGGAACAGAA CAATCTAATG TGTGGTTTGG G C C A C C G G T C G A C T G1921 GTCAAGTCCA AGATCGGCTC CACTGAGAAC CTGAAGCACC AGCCGGGAGG CGGGAAGGTG 1981 CAGATAATTA ATAAGAAGCT GGATCTTAGC AACGTCCAGT CCAAGTGTGG3601 CTTCCCACGG CCACTGCAGT CACCCCGTCT GCGCCGCTGT GCTGTTGTCT GCCGTGAGAG 3661 CCCAATCACT GCCTATACCC CTCATCACAC GTCACAATGT CCCGAATTCC5281 TACCTGAAAG GAAGTCTCTG GGCCCAGAAC TCTCCACCAA GAGCCTCCCT GCCGTTCGCT 5341 GAGTCCCAGC AATTCTCCTA AGTTGAAGGG ATCTGAGAAG GAGAAGGAAA G A E A S K T N L K721 TDHGAEIVYK SPVVSGDTSP RHLSNVSSTG SIDMVDSPQL ATLADEVSAS LAKQGL 1GCAGTCACCG CCACCCACCA GCTCCGGCAC CAACAGCAGC GCCGCTGCCA CCGCCCACCTG C C A T C T A C C C G T C C2161 AAAAGAGAAG GCAAGCTGGC AGGAGGGTGG CACTTCGTGG ATGACCTCCT TAGAAAAGAC 2221 TGACCTTGAT GTCTTGAGAG CGCTGGCCTC TTCCTCCCTC CCTGCAGGGT3841 AAGGGCCCTG CGACCACAGC AGGGATTGGG ATGAATTGCC TGTCCTGGAT CTGCTCTAGA 3901 GGCCCAAGCT GCCTGCCTGA GGAAGGATGA CTTGACAAGT CAGGAGACAC1 MAEPRQEFEV MEDHAGTYGL GDRKDQGGYT MHQDQEGDTD AGLKESPLQT PTEDGSEEPG61 SETSDAKSTP TAEAEEAGIG DTPSLEDEAA GHVTQARMVS KSKDGTGSDD KKAKGADGKT 121 KIATPRGAAP PGQKGQANAT RIPAKTPPAP KTPPSSGEPP KSGDRSGYSS PGSPGTPGSR Q H G G C T C A C T C G G C C A T C1981 AAAAGAGAAG GCAAGCTGGC AGGAGGGTGG CACTTCGTGG ATGACCTCCT TAGAAAAGAC 2041 TGACCTTGAT GTCTTGAGAG CGCTGGCCTC TTCCTCCCTC CCTGCAGGGT3661 AAGGGCCCTG CGACCACAGC AGGGATTGGG ATGAATTGCC TGTCCTGGAT CTGCTCTAGA 3721 GGCCCAAGCT GCCTGCCTGA GGAAGGATGA CTTGACAAGT CAGGAGACAC1 MAEPRQEFEV MEDHAGTYGL GDRKDQGGYT MHQDQEGDTD AGLKAEEAGI GDTPSLEDEA61 AGHVTQARMV SKSKDGTGSD DKKAKGADGK TKIATPRGAA PPGQKGQANA TRIPAKTPPA 121 PKTPPSSGEP PKSGDRSGYS SPGSPGTPGS RSRTPSLPTP PTREPKKVAV VRTPPKSPSS H G K K H D G T A K F K S I S P L L S D A P S L D F L T N S I F A KTKPREEQFNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKGLPSSIEKTISKAKGQPREP QVYTLPPSQEEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDGSF FLYSRLTVDKSRWQEGNVFSCSVMHEALHNHYTQKSLSLSLG

Claims

CLAIMS 1. A protein comprising one monovalent human transferrin receptor (TfR) binding domain, wherein the protein comprises two heavy chains HC1 and HC2 and one light chain LC1, and wherein the HC1, HC2 and LC1 comprise the following sequences: (a) HC1 comprises SEQ ID NO: 11, LC1 comprises SEQ ID NO: 10, HC2 comprises SEQ ID NO: 12, or (b) HC1 comprises SEQ ID NO: 13, LC1 comprises SEQ ID NO: 10, HC2 comprises SEQ ID NO:

14.

2. A conjugate comprising the protein of claim 1 and a therapeutic agent.

3. The conjugate of claim 2, wherein the therapeutic agent is selected from a double stranded RNA (dsRNA), oligonucleotide, polypeptide, small molecule, nanoparticle, lipid nanoparticle, exosome, antibody or antigen binding fragment thereof, or a combination thereof.

4. The conjugate of claim 2 or 3, wherein the therapeutic agent is linked to the protein through a linker.

5. The conjugate of any one of claim 2-4, wherein the therapeutic agent is a dsRNA.

6. The conjugate of claim 5, wherein the dsRNA comprises a sense strand and an antisense stand, wherein the antisense strand is complementary to a target mRNA selected from SNCA, MAPT, APP, ATXN2, ATXN3, SARM1, APOE, BACE1, FMR1, LRRK2, HTT, SOD1, SCN10A, SCN9A or CACNA1B mRNA.

7. The conjugate of claim 6, wherein the antisense strand is complementary to SNCA mRNA.

8. The conjugate of claim 6, wherein the antisense strand is complementary to MAPT mRNA.

9. The conjugate of any one of claims 4-8, wherein the linker is a Mal-Tet-TCO linker, SMCC linker, or GDM linker.

10. A conjugate of Formula (I): R-L-P, wherein R is a dsRNA comprising a sense stand and an antisense strand; wherein L is a linker, or optionally absent, wherein P is a protein comprising one monovalent human TfR binding domain, wherein P comprises two heavy chains HC1 and HC2 and one light chain LC1, and wherein the HC1, HC2 and LC1 comprise the following sequences: (c) HC1 comprises SEQ ID NO: 11, LC1 comprises SEQ ID NO: 10, HC2 comprises SEQ ID NO: 12, or (a) HC1 comprises SEQ ID NO: 13, LC1 comprises SEQ ID NO: 10, HC2 comprises SEQ ID NO:

14.

11. The conjugate of claim 4 or 10, wherein the linker is a Mal-Tet-TCO linker, SMCC linker, or GDM linker.

12. The conjugate of claim 11, wherein the linker is a SMCC linker.

13. The conjugate of any one of claims 10-12, wherein P is linked to the 3’ end of the sense strand of dsRNA, optionally via the linker.

14. The conjugate of any one of claims 10-13, wherein the antisense strand is complementary to a target mRNA selected from SNCA, MAPT, APP, ATXN2, ATXN3, SARM1, APOE, BACE1, FMR1, LRRK2, HTT, SOD1, SCN10A, SCN9A or CACNA1B mRNA.

15. The conjugate of claim 14, wherein the antisense strand is complementary to SNCA mRNA.

16. The conjugate of claim 7 or 15, wherein the sense strand and the antisense strand comprise a pair of nucleic acid sequences selected from the group consisting of:(a) the sense strand comprises SEQ ID NO: 26, and the antisense strand comprises SEQ ID NO: 27; (b) the sense strand comprises SEQ ID NO: 28, and the antisense strand comprises SEQ ID NO: 29; (c) the sense strand comprises SEQ ID NO: 30, and the antisense strand comprises SEQ ID NO: 31; (d) the sense strand comprises SEQ ID NO: 32, and the antisense strand comprises SEQ ID NO: 33; (e) the sense strand comprises SEQ ID NO: 34, and the antisense strand comprises SEQ ID NO: 35; (f) the sense strand comprises SEQ ID NO: 36, and the antisense strand comprises SEQ ID NO: 37; and (g) the sense strand comprises SEQ ID NO: 38, and the antisense strand comprises SEQ ID NO: 27, wherein optionally one or more nucleotides of the sense strand and the antisense strand are independently modified nucleotides, and wherein optionally one or more internucleotide linkages of the sense strand and the antisense strand are modified internucleotide linkages.

17. The conjugate of claim 14, wherein the antisense strand is complementary to MAPT mRNA.

18. The conjugate of claim 8 or 17, wherein the sense strand and the antisense strand comprise a pair of nucleic acid sequences selected from the group consisting of: (a) the sense strand comprises SEQ ID NO: 39, and the antisense strand comprises SEQ ID NO: 40; (b) the sense strand comprises SEQ ID NO: 41, and the antisense strand comprises SEQ ID NO: 42; and (c) the sense strand comprises SEQ ID NO: 43, and the antisense strand comprises SEQ ID NO: 44,wherein optionally one or more nucleotides of the sense strand and the antisense strand are independently modified nucleotides, and wherein optionally one or more internucleotide linkages of the sense strand and the antisense strand are modified internucleotide linkages.

19. The conjugate of any one of claims 6-18, wherein one or more nucleotides of the sense strand are modified nucleotides.

20. The conjugate of claim 19, wherein each nucleotide of the sense strand is a modified nucleotide.

21. The conjugate of any one of claims 6-20, wherein one or more nucleotides of the antisense strand are modified nucleotides.

22. The conjugate of claim 21, wherein each nucleotide of the antisense strand is a modified nucleotide.

23. The conjugate of any one of claims 19-22, wherein the modified nucleotide is a 2'-fluoro modified nucleotide, 2'-O-methyl modified nucleotide or 2’-O-C16alkyl nucleotide.

24. The conjugate of any one of claims 19-23, wherein the sense strand has four 2'-fluoro modified nucleotides at positions 7, 9, 10, and 11 from the 5’ end of the sense strand.

25. The conjugate of claim 24, wherein nucleotides at positions other than positions 7, 9, 10, and 11 of the sense strand are 2'-O-methyl modified nucleotides.

26. The conjugate of any one of claims 19-25, wherein the antisense strand has four 2'-fluoro modified nucleotides at positions 2, 6, 14, and 16 from the 5’ end of the antisense strand.

27. The conjugate of claim 26, wherein nucleotides at positions other than positions 2, 6, 14 and 16 of the antisense strand are 2'-O-methyl modified nucleotides.

28. The conjugate of any one of claims 19-23, wherein the sense strand has three 2'-fluoro modified nucleotides at positions 9, 10, and 11 from the 5’ end of the sense strand.

29. The conjugate of claim 28, wherein nucleotides at positions other than positions 9, 10, and 11 of the sense strand are 2'-O-methyl modified nucleotides.

30. The conjugate of any one of claims 19-25, 28, or 29, wherein the antisense strand has five 2'-fluoro modified nucleotides at positions 2, 5, 7, 14, and 16 from the 5’ end of the antisense strand.

31. The conjugate of claim 30, wherein nucleotides at positions other than positions 2, 5, 7, 14, and 16 of the antisense strand are 2'-O-methyl modified nucleotides.

32. The conjugate of any one of claims 19-25, 28, or 29, wherein the antisense strand has five 2'-fluoro modified nucleotides at positions 2, 5, 8, 14, and 16 from the 5’ end of the antisense strand.

33. The conjugate of claim 32, wherein nucleotides at positions other than positions 2, 5, 8, 14, and 16 of the antisense strand are 2'-O-methyl modified nucleotides.

34. The conjugate of any one of claims 19-25, 28, or 29, wherein the antisense strand has five 2'-fluoro modified nucleotides at positions 2, 3, 7, 14, and 16 from the 5’ end of the antisense strand.

35. The conjugate of claim 34, wherein nucleotides at positions other than positions 2, 3, 7, 14, and 16 of the antisense strand are 2'-O-methyl modified nucleotides.

36. The conjugate of any one of claims 6-35, wherein the sense strand and the antisense strand have one or more modified internucleotide linkages.

37. The conjugate of claim 36, wherein the modified internucleotide linkage is phosphorothioate linkage.

38. The conjugate of claim 36 or 37, wherein the sense strand has four or five phosphorothioate linkages.

39. The conjugate of any one of claims 36-38, wherein the antisense strand has four or five phosphorothioate linkages.

40. The conjugate of any one of claims 6-39, wherein the antisense strand has a phosphate analog at 5’ end.

41. The conjugate of claim 40, wherein the phosphate analog is 5’-vinylphosphonate.

42. The conjugate of any one of claims 6-41, wherein the sense strand comprises an abasic moiety or inverted abasic moiety.

43. The conjugate of any one of claims 7, 15, 16, 19-42, wherein the sense strand and the antisense strand comprise a pair of nucleic acid sequences selected from the group consisting of: (a) the sense strand comprises SEQ ID NO: 45, and the antisense strand comprises SEQ ID NO: 46; (b) the sense strand comprises SEQ ID NO: 47, and the antisense strand comprises SEQ ID NO: 48; (c) the sense strand comprises SEQ ID NO: 47, and the antisense strand comprises SEQ ID NO: 49; (d) the sense strand comprises SEQ ID NO: 47, and the antisense strand comprises SEQ ID NO: 50; (e) the sense strand comprises SEQ ID NO: 51, and the antisense strand comprises SEQ ID NO: 46; (f) the sense strand comprises SEQ ID NO: 52, and the antisense strand comprises SEQ ID NO: 53; (g) the sense strand comprises SEQ ID NO: 54, and the antisense strand comprises SEQ ID NO: 55; (h) the sense strand comprises SEQ ID NO: 56, and the antisense strand comprises SEQ ID NO: 57;(i) the sense strand comprises SEQ ID NO: 58, and the antisense strand comprises SEQ ID NO: 59; (j) the sense strand comprises SEQ ID NO: 60, and the antisense strand comprises SEQ ID NO: 59; (k) the sense strand comprises SEQ ID NO: 61, and the antisense strand comprises SEQ ID NO: 49; and (l) the sense strand comprises SEQ ID NO: 62, and the antisense strand comprises SEQ ID NO:

49.

44. The conjugate of any one of claims 7, 15, 16, 19-43, wherein the sense strand and the antisense strand have a pair of nucleic acid sequences selected from the group consisting of: (a) the sense strand consists of SEQ ID NO: 45, and the antisense strand consists of SEQ ID NO: 46; (b) the sense strand consists of SEQ ID NO: 47, and the antisense strand consists of SEQ ID NO: 48; (c) the sense strand consists of SEQ ID NO: 47, and the antisense strand consists of SEQ ID NO: 49; (d) the sense strand consists of SEQ ID NO: 47, and the antisense strand consists of SEQ ID NO: 50; (e) the sense strand consists of SEQ ID NO: 51, and the antisense strand consists of SEQ ID NO: 46; (f) the sense strand consists of SEQ ID NO: 52, and the antisense strand consists of SEQ ID NO: 53; (g) the sense strand consists of SEQ ID NO: 54, and the antisense strand consists of SEQ ID NO: 55; (h) the sense strand consists of SEQ ID NO: 56, and the antisense strand consists of SEQ ID NO: 57; (i) the sense strand consists of SEQ ID NO: 58, and the antisense strand consists of SEQ ID NO: 59;(j) the sense strand consists of SEQ ID NO: 60, and the antisense strand consists of SEQ ID NO: 59; (k) the sense strand consists of SEQ ID NO: 61, and the antisense strand consists of SEQ ID NO: 49; and (l) the sense strand consists of SEQ ID NO: 62, and the antisense strand consists of SEQ ID NO:

49.

45. The conjugate of any one of claims 8, 17-42, wherein the sense strand and the antisense strand comprise a pair of nucleic acid sequences selected from the group consisting of: (a) the sense strand comprises SEQ ID NO: 63, and the antisense strand comprises SEQ ID NO: 64; (b) the sense strand comprises SEQ ID NO: 65, and the antisense strand comprises SEQ ID NO: 66; (c) the sense strand comprises SEQ ID NO: 67, and the antisense strand comprises SEQ ID NO: 68; (d) the sense strand comprises SEQ ID NO: 69, and the antisense strand comprises SEQ ID NO: 70; (e) the sense strand comprises SEQ ID NO: 71, and the antisense strand comprises SEQ ID NO: 72; and (f) the sense strand comprises SEQ ID NO: 73, and the antisense strand comprises SEQ ID NO:

74.

46. The conjugate of any one of claims 8, 17-42, 45, wherein the sense strand and the antisense strand comprise a pair of nucleic acid sequences selected from the group consisting of: (a) the sense strand consists of SEQ ID NO: 63, and the antisense strand consists of SEQ ID NO: 64; (b) the sense strand consists of SEQ ID NO: 65, and the antisense strand consists of SEQ ID NO: 66; (c) the sense strand consists of SEQ ID NO: 67, and the antisense strand consists of SEQ ID NO: 68;(d) the sense strand consists of SEQ ID NO: 69, and the antisense strand consists of SEQ ID NO: 70; (e) the sense strand consists of SEQ ID NO: 71, and the antisense strand consists of SEQ ID NO: 72; and (f) the sense strand consists of SEQ ID NO: 73, and the antisense strand consists of SEQ ID NO:

74.

47. A pharmaceutical composition comprising the protein of claim 1 or the conjugate of any one of claims 2-46, and a pharmaceutically acceptable carrier.

48. A method of treating a CNS disease in a patient in need thereof, the method comprising administering to the patient an effective amount of the conjugate of any one of claims 2- 46, or the pharmaceutical composition of claim 47.

49. A method of treating a neurodegenerative synucleinopathy in a patient in need thereof, the method comprising administering to the patient an effective amount of the conjugate of any one of claims 7, 15, 16, 19-44.

50. The method of claim 49, wherein the neurodegenerative synucleinopathy is Parkinson’s disease, Alzheimer’s disease, multiple system atrophy, or Lewy body dementia.

51. A method of treating a tauopathy in a patient in need thereof, the method comprising administering to the patient an effective amount of the conjugate of any one of claims 8, 17-42, 45, 46.

52. The method of claim 51, wherein the tauopathy is Alzheimer’s disease, frontotemporal dementia (FTD), frontotemporal dementia with parkinsonism linked to chromosome 17 (FTDP-17), frontotemporal lobar degeneration (FTLD), behavioral variant frontotemporal dementia (bvFTD), nonfluent variant primary progressive aphasia (nfvPPA), Parkinson’s discase, Pick’s disease (PiD), primary progressive aphasia - semantic (PPA-S), primary progressive aphasia - logopenic (PPA-L), multiple system tauopathy with presenile dementia (MSTD), neurofibrillary tangle (NFT) dementia, FTDwith motor neuron disease, progressive supranuclear palsy (PSP), amyotrophic lateral sclerosis / parkinsonism-dementia complex (ALS-PDC), argyrophilic grain dementia (AGD), British type amyloid angiopathy, cerebral amyloid angiopathy, chronic traumatic encephalopathy (CTE), corticobasal degeneration (CBD), Creutzfeldt-Jakob disease (CJD), dementia pugilistica, diffuse neurofibrillary tangles with calcification, Down’s syndrome, epilepsy, Gerstmann-Straussler-Scheinker disease, Hallervorden-Spatz disease, Huntington’s disease, inclusion body myositis, lead encephalopathy, Lytico- Bodig disease, meningioangiomatosis, multiple system atrophy, myotonic dystrophy, Niemann-Pick disease type C (NP-C), non-Guamanian motor neuron disease with neurofibrillary tangles, postencephalitic parkinsonism, prion protein cerebral amyloid angiopathy, progressive subcortical gliosis, tangle only dementia, tangle-predominant dementia, ganglioglioma, gangliocytoma, subacute sclerosingpan encephalitis, tuberous sclerosis, lipofuscinosis, primary age-related tauopathy (PART), or globular glial tauopathies (GGT).

53. The method of any one of claims 48-52, wherein the conjugate or composition is administered to the patient intravenously or subcutaneously.

54. The conjugate of any one of claims 2-46, or the pharmaceutical composition of claim 47, for use in a therapy.

55. The conjugate of any one of claims 7, 15, 16, 19-44, for use in the treatment of a neurodegenerative synucleinopathy.

56. The conjugate or pharmaceutical composition for use of claim 55, wherein the neurodegenerative synucleinopathy is Parkinson’s disease, Alzheimer’s disease, multiple system atrophy, or Lewy body dementia.

57. The conjugate of any one of claims 8, 17-42, 45, 46, for use in the treatment of a tauopathy.

58. The conjugate or pharmaceutical composition for use of claim 57, wherein the tauopathy is Alzheimer’s disease, frontotemporal dementia (FTD), frontotemporal dementia withparkinsonism linked to chromosome 17 (FTDP-17), frontotemporal lobar degeneration (FTLD), behavioral variant frontotemporal dementia (bvFTD), nonfluent variant primary progressive aphasia (nfvPPA), Parkinson’s discase, Pick’s disease (PiD), primary progressive aphasia - semantic (PPA-S), primary progressive aphasia - logopenic (PPA- L), multiple system tauopathy with presenile dementia (MSTD), neurofibrillary tangle (NFT) dementia, FTD with motor neuron disease, progressive supranuclear palsy (PSP), amyotrophic lateral sclerosis / parkinsonism-dementia complex (ALS-PDC), argyrophilic grain dementia (AGD), British type amyloid angiopathy, cerebral amyloid angiopathy, chronic traumatic encephalopathy (CTE), corticobasal degeneration (CBD), Creutzfeldt- Jakob disease (CJD), dementia pugilistica, diffuse neurofibrillary tangles with calcification, Down’s syndrome, epilepsy, Gerstmann-Straussler-Scheinker disease, Hallervorden-Spatz disease, Huntington’s disease, inclusion body myositis, lead encephalopathy, Lytico-Bodig disease, meningioangiomatosis, multiple system atrophy, myotonic dystrophy, Niemann-Pick disease type C (NP-C), non-Guamanian motor neuron disease with neurofibrillary tangles, postencephalitic parkinsonism, prion protein cerebral amyloid angiopathy, progressive subcortical gliosis, tangle only dementia, tangle-predominant dementia, ganglioglioma, gangliocytoma, subacute sclerosingpan encephalitis, tuberous sclerosis, lipofuscinosis, primary age-related tauopathy (PART), or globular glial tauopathies (GGT).

59. Use of the conjugate of any one of claims 2-46 in the manufacture of a medicament for treating a CNS disease.

60. Use of the conjugate of any one of claims 7, 15, 16, 19-44 in the manufacture of a medicament for treating a neurodegenerative synucleinopathy.

61. The use of claim 60, wherein the neurodegenerative synucleinopathy is Parkinson’s disease, Alzheimer’s disease, multiple system atrophy, or Lewy body dementia.

62. Use of the conjugate of any one of claims 8, 17-42, 45, 46, in the manufacture of a medicament for treating a tauopathy.

3. The use of claim 62, wherein the tauopathy is Alzheimer’s disease, frontotemporal dementia (FTD), frontotemporal dementia with parkinsonism linked to chromosome 17 (FTDP-17), frontotemporal lobar degeneration (FTLD), behavioral variant frontotemporal dementia (bvFTD), nonfluent variant primary progressive aphasia (nfvPPA), Parkinson’s discase, Pick’s disease (PiD), primary progressive aphasia - semantic (PPA-S), primary progressive aphasia - logopenic (PPA-L), multiple system tauopathy with presenile dementia (MSTD), neurofibrillary tangle (NFT) dementia, FTD with motor neuron disease, progressive supranuclear palsy (PSP), amyotrophic lateral sclerosis / parkinsonism-dementia complex (ALS-PDC), argyrophilic grain dementia (AGD), British type amyloid angiopathy, cerebral amyloid angiopathy, chronic traumatic encephalopathy (CTE), corticobasal degeneration (CBD), Creutzfeldt-Jakob disease (CJD), dementia pugilistica, diffuse neurofibrillary tangles with calcification, Down’s syndrome, epilepsy, Gerstmann-Straussler-Scheinker disease, Hallervorden-Spatz disease, Huntington’s disease, inclusion body myositis, lead encephalopathy, Lytico- Bodig disease, meningioangiomatosis, multiple system atrophy, myotonic dystrophy, Niemann-Pick disease type C (NP-C), non-Guamanian motor neuron disease with neurofibrillary tangles, postencephalitic parkinsonism, prion protein cerebral amyloid angiopathy, progressive subcortical gliosis, tangle only dementia, tangle-predominant dementia, ganglioglioma, gangliocytoma, subacute sclerosingpan encephalitis, tuberous sclerosis, lipofuscinosis, primary age-related tauopathy (PART), or globular glial tauopathies (GGT).