Novel peptide, applications and preparation method thereof
A new type of technology, applied in the field of pharmacy and medicine, can solve the problem of dangerous self-antigen, and achieve the effect of reducing the incidence rate, delaying the disease process, and maintaining weight stability.
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Embodiment 1
[0024] Embodiment 1: the preparation process of novel peptide
[0025] Synthesize a novel peptide whose amino acid sequence is: HGDTTFEYQDIPALDSLTPANED (named IA-2-P2, see SEQNO.1), and its specific flow chart is shown in Figure 4 ; P277 (VLGGGCALLRCIPALDSLTPANED, see SEQ NO.2); P2 (T epitope sequence in P277, IPALDSLTPANED, see SEQ NO.3), the above peptides were all synthesized by Jill Biochemical Shanghai Co., Ltd. using FMOC solid phase synthesis, HPLC Detected purity >90%.
[0026] Its specific preparation method is as follows:
[0027] 1. Resin selection
[0028] Peptides are connected from the C-terminus to the N-terminus, so the synthesis of peptides is reversed in sequence. First select Fmoc-Asp(Otbu)-OH Wang Resin;
[0029] 2. Removal of Fmoc
[0030] Before each next amino acid is connected, the protecting group on the amino group of the previous amino acid must be removed. Add the prepared deprotection solution (20% hexahydropyridine and 80% DMF) into the rea...
Embodiment 2
[0037] Example 2: Pharmacodynamic evaluation of novel peptide IA-2-P2
[0038] 1. Animal immunity
[0039]Sixty 4-week-old female non-obese diabetic (NOD / Lt) mice (purchased from Shanghai Slaccas Experimental Animal Center (Slaccas Experimental Animal), license number: SCXK 2003-0003.) were randomly divided into 5 groups, 12 in each group. Only, respectively: control group (blank control group), placebo group (solvent control group, negative control group), P277 group (positive control group), P2 group (positive control group), IA-2-P2 group. Before administration, the oil preparation is temporarily prepared according to the ratio of 1 mg polypeptide + 40 mg mannitol dissolved in 1 ml 20% Lipofundin. At the age of 4, 7, and 10 weeks, they were injected subcutaneously, three times in total. The drug concentration in the administration group was 1 mg / ml, and the dosage was 80 μg / animal / time, that is, 80 μl liquid medicine; the negative control group: 80 μl oil / animal / time.
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