Insulin analog complex with reduced affinity for insulin receptor and use thereof

A technology for insulin and conjugates, applied in the field of conjugates of insulin analogs, can solve the problems of no specificity, reduced activity, no change in binding affinity, etc.

Active Publication Date: 2019-12-03
HANMI PHARMA
View PDF10 Cites 2 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, in J Pharmacol Exp Ther (1998) 286: 959, Diabetes Care (1990) 13: 923, the proposed insulin analogues had at least two amino acid substitutions or did not provide specific results, while in Diabetes (1990) 39:1033, insulin analogs showed no change in their binding affinity to the receptor, or their activity was reduced by substitution of amino acids directly involved in binding to the insulin receptor

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Insulin analog complex with reduced affinity for insulin receptor and use thereof
  • Insulin analog complex with reduced affinity for insulin receptor and use thereof
  • Insulin analog complex with reduced affinity for insulin receptor and use thereof

Examples

Experimental program
Comparison scheme
Effect test

preparation example Construction

[0210] Insulin analogs can be readily prepared by those skilled in the art using peptide preparation methods known in the art. For example, insulin analogs can be produced by a method comprising the steps of:

[0211] a) expressing an insulin analog by culturing a transformant comprising a nucleic acid encoding the insulin analog; and

[0212] b) Isolation and purification of the expressed insulin analog.

[0213] The medium used for culturing the transformant of the present invention can meet the requirements of host cell culture in an appropriate manner. The carbon source contained in the medium used for host cell growth can be appropriately selected by those skilled in the art according to the transformants prepared therefrom, and appropriate culture conditions can be selected to control the period and amount of culture.

[0214] Examples of sugar sources used may include sugars and carbohydrates such as glucose, sucrose, lactose, fructose, maltose, starch and cellulose; ...

Embodiment 1

[0327] Embodiment 1: Preparation of single-chain insulin analog expression vector

[0328] For the preparation of insulin analogues with a single modified amino acid in the A or B chains, respectively, using the native insulin expression vector in possession as a template, forward and reverse oligonucleotides were synthesized (Table 2) and then PCR amplified analogs for each gene.

[0329] Amino acid sequences and analog names modified in the A chain or B chain are shown in Table 1 below. In Table 1, analog 1 represents the analog in which the 14th amino acid (i.e. tyrosine, Y) of the A chain is replaced by histidine (H), and analog 6 represents the 16th amino acid in the B chain ( That is, an analogue in which tyrosine, Y) is replaced by glutamic acid (E).

[0330] [Table 1]

[0331]

[0332]

[0333] Primers used for insulin analog amplification are shown in Table 2 below.

[0334] [Table 2]

[0335]

[0336]

[0337] Eighteen repeated cycles of PCR reacti...

Embodiment 2

[0347] Example 2: Expression of Recombinant Insulin Analog Fusion Peptides

[0348] Expression of recombinant insulin analogues was performed under the control of the T7 promoter. Escherichia coli BL21-DE3 (Escherichia coli B F-dcm ompT hsdS(rB-mB-)galλDE3; Novagen) was transformed with each recombinant insulin analog expression vector. Transformations were performed according to the recommended protocol (Novagen). A single colony transformed with each recombinant expression vector was collected, inoculated into 2X Luria broth (LB) containing ampicillin (50 μg / mL), and incubated at 37°C for 15 hours. Mix the recombinant strain culture broth and 2X LB medium containing 30% glycerol at a ratio of 1:1 (v / v), dispense 1 mL of each mixture into cryovials, and store at -140 °C, which is used Used as a cell stock solution for the production of recombinant fusion proteins.

[0349] For expression of recombinant insulin analogues, one vial of each cell stock was thawed and inocula...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

PropertyMeasurementUnit
molecular weightaaaaaaaaaa
molecular weightaaaaaaaaaa
Login to view more

Abstract

The present invention relates to an insulin analog complex and use thereof.

Description

technical field [0001] The present invention relates to conjugates of insulin analogues and uses thereof. Background technique [0002] It is known that proteins in the body are removed through various routes, including decomposition by proteases in the blood, excretion through the kidneys, removal through receptors, and the like. In this regard, various attempts have been made to improve the therapeutic effect of proteins by avoiding protein clearance mechanisms to increase the half-life of physiological proteins. [0003] In general, insulin is a hormone secreted by the pancreas of the human body, which regulates blood sugar levels and has the effect of maintaining normal blood sugar levels while carrying excess glucose in the blood to cells to provide energy for the cells. However, in diabetics, insulin does not work properly due to insulin deficiency, resistance to insulin and loss of beta cell function. As a result, diabetic patients cannot utilize blood sugar as an e...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
Patent Type & Authority Applications(China)
IPC IPC(8): C07K14/62A61K38/00A61K47/56A61K47/68
CPCA61K38/00A61K47/68C07K14/62A61K47/60A61K47/56A61K47/6883A61P3/10
Inventor 朴永振崔仁荣郑圣烨权世昌
Owner HANMI PHARMA
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap