Polypeptide capable of treating Alzheimer's disease and vaccine containing polypeptide capable of treating Alzheimer's disease
A technology for Alzheimer's disease and polypeptide vaccine, applied in the field of protein engineering, can solve problems such as insecurity, and achieve the effects of prolonging survival, preventing the formation and accumulation of β-amyloid, and having extensive clinical application value.
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Embodiment 1
[0025] Example 1: Polypeptide Synthesis by Solid Phase Polypeptide Synthesis
[0026] All the reagents used below were purchased from Jill Biochemical (Shanghai) Co., Ltd.;
[0027] 1. Take 1.5g of dichloro resin, add it to the reaction column soaked in DCM, soak in 15ml of DCM for 30min to fully expand the resin, and activate it for use;
[0028] 2. Weigh 0.31g of Fmoc-Cys(Acm).OH and dissolve it in DCM, then add 0.5ml of DIEA and mix it into the reaction vessel, blow N 2 After reacting for 2 hours, filter the reaction solution, add 5ml of MeOH to block the reaction for 1 hour, and then wash with DCM, isopropanol and DMF for 3 times;
[0029] 3. Remove the amino protecting group: add about 15ml of 20% piperidine in DMF solution for 5 minutes, filter, then add 15ml and react for 20 minutes, wash the resin twice with isopropanol, and wash the resin 3 times with DMF;
[0030] 4. Formation of peptide bonds: Weigh 0.55g Fmoc-Trp(600)-OH, dissolve 0.35g TBTU in DMF, mix with 0.6m...
Embodiment 2
[0032] Example 2: Polypeptide Synthesis by Solid-Phase Polypeptide Synthesis
[0033] The peptide synthesizer adopts the American AB1431A model, and the peptide solid-phase synthesis, resin selection and activation treatment are purchased from Jill Biochemical (Shanghai) Co., Ltd.
[0034] Peptide synthesis is actually a process of repeated addition of amino acids, and the synthesis is generally synthesized from the carboxyl terminal (C-terminal) to the amino-terminal (N-terminal). The basic principle of solid-phase synthesis of peptides is: use insoluble polymer resin as a solid-phase carrier, first link an amino acid containing an amino group protected by a blocking group on the solid-phase carrier with a covalent bond, and then use trifluoroacetic acid as a deprotection agent. Reagent, remove the protecting group of the amino group, so that the first amino acid is connected on the solid support. Activate the carboxyl group of the second amino acid with a protective group b...
Embodiment 3
[0045] Embodiment three: adopt genetic recombination synthetic polypeptide
[0046] Use genetic engineering technology to use probiotics and yeast to secrete and produce the polypeptide drug of the present invention, and use methods such as yogurt, solid drinks, beer, etc. to use probiotics and yeast to grow and reproduce in the intestinal tract to continuously secrete and produce various diseases. Preventive and therapeutic Peptide drugs. Apply genetic engineering technology to construct probiotics and yeast polypeptide drug and vaccine vectors, and clone antigen genes and cytokine genes to probiotics and yeast plasmids. After the transformation of probiotics and yeast, the peptide drug products containing the expression of the target gene are screened out and used as seed peptide drugs for cryopreservation, and the seed peptide drugs are scaled up for cultivation.
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