Micro-molecule polypeptide and application thereof
A technology for small molecular polypeptides and uses, which is applied in the fields of peptides, medical preparations containing active ingredients, peptide/protein components, etc., to achieve the effects of obvious application potential, simple synthesis method, and easy large-scale production.
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Embodiment 1
[0016] A small molecular polypeptide, the amino acid sequence of the small molecular polypeptide is shown in SEQ ID No.1;
[0017] SEQ ID No. 1: ICKKMMKKSTLLQDDIL.
[0018] The isoelectric point of the small molecule polypeptide is 9.7.
[0019] The molecular weight of the small molecule polypeptide is 2008.54g / mol.
[0020] The preparation method of the small molecule polypeptide:
[0021] Select amino acid-king resin as the carrier (resin), fully swell the resin with dichloromethane, wash several times with dimethylformamide, use DBLK of appropriate concentration to remove the Fmoc-protecting group, and then use dimethylformamide to remove the Fmoc-protecting group. The amide was washed several times to remove DBLK, and the appropriate condensing agent benzotriazole-N,N,N',N'-tetramethyluronium hexafluorophosphate, the activator methylmorpholine and the C-terminal Two Fmoc-protected amino acids (Fmoc-Pro-OH) are coupled, detected by ninhydrin detection method to ensure th...
Embodiment 2
[0023] Determination of α-glucosidase activity of small molecule polypeptides in vitro.
[0024] All tests were carried out with a Microplate reader ELX808TM microplate reader (BioTek, USA) at 37°C. The data analysis software uses Origin software for data processing, and uses acarbose as a reference substance.
[0025] (1) Preparation of inhibitor stock solution: the tested inhibitors were formulated into 10 mM DMSO solution (the DMSO solution of the polypeptide of Example 1).
[0026] (2) Preparation of enzyme stock solution: α-glucosidase was purchased from Sigma Company of the United States; 1 mg / mL was prepared respectively with phosphate buffer solution of pH=6.8.
[0027] (3) Preparation of substrate stock solution: p-nitrophenyl glucoside (PNPG) was used as substrate, purchased from Sigma Company; 10 mg / mL was prepared respectively with phosphate buffer solution of pH=6.8.
[0028] (4) Preparation of stop solution: Sodium carbonate (Na2CO3) was purchased from Shanghai...
Embodiment 3
[0038] Take 0.1 ml of the DMSO solution (0.2, 0.4, 0.6, 0.8 μg / ml) of the polypeptide of Example 1 and add it to 8 ml of 0.004% 1,1-diphenyl-2-trinitrophenylhydrazine (DPPH) solution . Absorbance was measured at the maximum wavelength (517nm) until equilibrium. The formula for calculating the clearance rate is as follows:
[0039] S%=(1-A 样品 ) / A 空白 ×100%. Among them, A 空白 Absorbance of DPPH solution without adding peptide DMSO solution, A 样品 is the absorbance of the DPPH solution added to the DMSO solution of the compound. The result is as figure 1 shown. It can be seen that the polypeptide molecule of the present invention has excellent antioxidant performance, and the scavenging ability for DPPH free radicals can reach more than 99.5% at a relatively low concentration.
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