Engineer chimeric receptors to activate myeloid cells, resolving immunosuppression and enhancing anti-tumor immunity.
Non-classical MHC Ib peptide vaccines utilize HLA-E, HLA-F, and HLA-G molecules to present antigens across all human populations.
Segmented single-chain variable fragments assemble into multispecific complexes, resolving production complexity while retaining Ig function.
Merging distinct enzymatic domains into a single chimeric molecule overcomes limited bacteriolytic activity against antibiotic-resistant Gram-positive strains.
Nucleic acid molecules encode Zika virus prM and E proteins for virus-like particle production.
A chemically defined serum-free medium expands T cell populations using specific nutrient ratios.
Segmented CAR designs with specific recognition domains eliminate T-cell leukemia while managing structural complexity.
Engineered MAD2019-H848A nickase fusion proteins combine reverse transcriptase activity to enable precise nucleic acid editing.
Recombinant virion arrays display human membrane proteins in native conformations for high-throughput screening.
Engineering yeast with Msn4/2 transcription factors to overcome expression bottlenecks and increase recombinant protein titer.
Transient Pichia pastoris expression yields highly immunogenic haemagglutinin antigen without protein contamination or virus contact.
A human ADARB2-derived RMAD1 peptide enables high-efficiency cargo molecule delivery into cells.
A furin-cleavable delivery construct uses a transcytosing element to transport therapeutic cargo across epithelial barriers.
A peptide accumulates in cancer stroma to deliver anticancer drugs.
A ribonucleoprotein complex directs demethylation activity to specific genomic loci using a three-component hybrid system.
A synthetic plasmid DNA vaccine uses codon optimization and a human IgG2 signal peptide to express the SARS-CoV-2 spike glycoprotein.
A synthetic suicide genetic circuit uses riboswitches to activate cell death in non-producing strains.
Recombinant host cells employ multiple distinct secretion signals to direct protein production through separate cellular pathways.
Fusing Gam protein to base editors binds double-stranded DNA breaks and prevents indel formation.
A Kinesin-derived Angiogenesis Inhibitor peptide blocks VEGFR2 receptor trafficking to the cell surface.
P329G-modified heterodimeric Fc antibodies bridge tumor antigens and CAR-T cells, reducing off-target toxicity while enhancing anti-cancer efficacy.
TAT-fusion proteins block SNARE complex formation to inhibit neutrophil degranulation.
Genetically-encoded voltage indicators resolve the gap in studying internal electrical signals of mitochondria and endoplasmic reticulum membranes.
Engineered pericytes stably express soluble TRAIL, resolving toxicity and short half-life issues of recombinant proteins.
ITAM deletion and spacing optimization in CD3 zeta chains increase cytolytic activity against low-affinity cancer antigens.
Chemically modified peptides bind FoxP3 to block Treg immunosuppression, reducing autoimmune disease risk while enhancing antitumor response.
Engineering CAR T cells to recognize IL13Rα2 resolves the trade-off between tumor destruction and toxicity to normal tissues.
Pegylated IL-10 agents enhance CD8+ T cell function and survival during chimeric antigen receptor therapy.
Jchain-specific T cell receptors recognize multiple myeloma cells via HLA presentation, preventing antigen escape variants that cause relapse.
Pre-selecting naïve and stem memory T cells expands high-potency populations, reducing severe cytokine release syndrome and neurotoxicity.
Antigen-binding proteins target HLA-displayed HPV 16 E7 peptides to enable precise molecular recognition of infected cells.
Targeted mutations in Cas9 residues lower off-target binding affinity while preserving on-target cleavage efficiency for precise genome editing.
Chimeric transmembrane receptors oligomerize upon extramembrane signal detection to activate intracellular pathways.
Optimizing ADP-ribosyl transferase C3 fusion protein manufacturing through controlled cultivation and sequential chromatography steps.
Codon-optimized mRNA encoding Cas9 reduces cytokine elevation while increasing genome editing efficiency.
A reversed universal chimeric antigen receptor redirects immune cells using modular adapter molecules to recognize diverse peptide epitope tags.
PCSK9 enables lysosomal enzyme targeting to skeletal muscle, resolving poor cellular uptake in Pompe disease.
Fusing CBM3 to carbonic anhydrase enables selective capture on cellulose beads, bypassing complex separation steps in plant-based production.
Engineered zinc finger nucleases target BCL11A enhancer sequences to reduce off-target cleavage and sustain gamma globin expression.
A Cas-based targeting system fused with light-sensitive receptors induces controlled protein clustering at specific genomic loci.
Cell-penetrating polypeptides block IRF5 nuclear localization, reducing pro-inflammatory cytokine expression and side effects in systemic lupus erythematosus.
TNFRSF transmembrane domains in chimeric antigen receptors increase T cell persistence and cytolysis despite rapid post-infusion disappearance.
A packaging system integrates adenoviral genes into host cells to eliminate helper virus contamination during vector production.
Engineered chimeric antigen receptors bridge T-cells and solid tumors, overcoming limited chemotherapy effectiveness.
Engineering a CD21-specific binding domain enables selective recognition of T-ALL cells while sparing normal T-cells from fratricide.
Removing specific ITAM motifs from CD3ζ chains prevents T cell exhaustion, sustaining immune responses against cancer targets.
Replacing the GPI anchor with a transmembrane domain directs modified antigens to endosomes, resolving low immunogenicity caused by membrane anchoring.
Armored CAR immune cells secrete bispecific antibodies to recruit T cells against p95HER2-expressing tumors.
Preliminary IL-1Ra administration mitigates cytokine release syndrome and neurotoxicity during BCMA CAR T cell therapy, enabling higher response rates.