Use and modification method of modified peptide in preparation of drug for inhibiting insulin secretion from pancreatic islets

An insulin and pancreatic islet technology, applied in the field of peptide modification, can solve the problems of patient suffering, unstable polypeptide drugs, affecting the application of COX, etc., and achieve the effect of enhancing resistance

Active Publication Date: 2022-05-10
SOUTH CENTRAL UNIVERSITY FOR NATIONALITIES
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] (1) Linear peptide COX synthesized by solid-phase synthesis 52-69 Inability to function by oral administration;
[0005] (2) There is no linear peptide COX in the prior art 52-69 Methods for modifying the molecular structure that affect COX 52-69 Applications
[0009] Due to their instability and low bioavailability, peptide drugs are mostly administered by injection, which brings great pain to patients

Method used

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  • Use and modification method of modified peptide in preparation of drug for inhibiting insulin secretion from pancreatic islets
  • Use and modification method of modified peptide in preparation of drug for inhibiting insulin secretion from pancreatic islets
  • Use and modification method of modified peptide in preparation of drug for inhibiting insulin secretion from pancreatic islets

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Experimental program
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Effect test

Embodiment 1

[0052] First select closed COX 52-69 N-terminal acetylation, C-terminal amidation modification, reducing the total charge at both ends of the polypeptide, making it closer to the parent protein, and enhancing resistance to endopeptidases. After incubation with simulated gastrointestinal fluid in vitro, it was found by HPLC-MS that the short peptide COX 52-69 It is digested into two short peptides "LLPAGWV" and "LSHLDSYKKRE".

[0053] In order to make it stably exist in the simulated gastrointestinal fluid, the present invention methylates the amide bond between valine and leucine, and adds cysteine ​​at both ends of the polypeptide at the same time, and makes it pass through two The sulfur bonds connect to form a ring, making it a rigid molecule. After incubation with simulated gastrointestinal fluid in vitro, it was found by HPLC-MS that the short peptide COX 52-69 Can exist stably in simulated gastrointestinal fluid.

Embodiment 2

[0055] To confirm the modified short peptide COX 52-69 It still has the function of inhibiting glucose-induced insulin secretion, and the COX modified by methylation and cyclization was detected by ELISA. 52-69 Tissue supernatants from the incubated islets were assayed. It can be seen from the statistical results that the modified peptide COX 52-69 It still has the function of inhibiting glucose-induced insulin secretion.

[0056] At the same time, in order to verify the modified peptide COX 52-69 Through the intestinal mucosa, the present invention constructs the Caco-2 cell model in vitro, and the modified peptide COX 52-69 The transmembrane transport ability was tested. The modified peptide COX was found by evaluating its apparent permeability coefficient (Papp) 52-69 Good transmembrane transport ability.

[0057] It can be confirmed by the above experiments that the modified peptide COX 52-69 It still has the function of inhibiting glucose-induced insulin secretion,...

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Abstract

The invention belongs to the technical field of peptide modification, and discloses the use and modification method of a modified peptide in the preparation of a drug for inhibiting insulin secretion from pancreatic islets. The selective blocking of COX 52‑69 the end of; for closed COX 52‑69 N-terminal acetylation and C-terminal amidation modification; methylation modification on the amide bond between valine and leucine, and addition of cysteine ​​at both ends of the polypeptide, and make it through two The sulfur bonds connect into rings, forming a rigid molecule. The present invention transforms the original linear polypeptide into a circular polypeptide COX 52‑69 , so that in the past, only the way of injection can be changed to oral administration, and it also has the function of inhibiting glucose-induced insulin secretion. Modified cyclic peptides, realizing oral administration route, and more linear peptide COX 52‑69 It has the same function of inhibiting insulin secretion from pancreatic islets. The oral administration route of the polypeptide is realized.

Description

technical field [0001] The invention belongs to the technical field of peptide modification, and in particular relates to the use and modification method of a modified peptide in the preparation of a drug for inhibiting insulin secretion from pancreatic islets. Background technique [0002] Currently, the short peptide COX 52-69 It is a polypeptide containing 18 amino acids. It was originally isolated and purified from the small intestine of pigs. After the amino acid sequence alignment, it was found that it completely overlapped with the 52nd to 69th of cytochrome oxidase VIII, so it was named COX 52-69 . Its sequence is LLPAGWVLSHLDSYKKRE. COX obtained by biochemical separation and purification 52-69 The functional experiment of the polypeptide found that the polypeptide can inhibit the secretion of insulin caused by glucose. This discovery has applied for a Chinese invention patent on October 11, 2013, and the application number is 201310471571.9. Afterwards, the shor...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C12N9/02C07K1/107A61K38/44A61P5/00A61P3/08
CPCC12N9/0053C12Y109/03001A61P5/00A61P3/08A61K38/00
Inventor 李臣鸿李知宗
Owner SOUTH CENTRAL UNIVERSITY FOR NATIONALITIES
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