Method for improving recombinant human albumin expression quality and reducing degradation and application

A technology for human albumin and mass reduction, applied in the field of genes, can solve problems such as affecting the quality of recombinant proteins in purification work, and achieve the effect of reducing wrong shearing and improving protein quality

Inactive Publication Date: 2020-07-03
TONGHUA ANRATE BIOPHARMACEUTICAL CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0002] The yeast expression system has the advantages of high fermentation density, strong secretion ability, and low degree of glycosylation, but the expression of foreign protein is also accompanied by the expression of a certain amount of protease, so that the expressed foreign protein is degraded to varying degrees. Directly affect the subsequent purification work and the quality of recombinant protein

Method used

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  • Method for improving recombinant human albumin expression quality and reducing degradation and application
  • Method for improving recombinant human albumin expression quality and reducing degradation and application
  • Method for improving recombinant human albumin expression quality and reducing degradation and application

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0132] Example 1 Construction of engineering bacteria containing only human albumin gene

[0133] Recombinant Engineering Bacteria I

[0134] The transformed recombinant plasmid is pPic9-HSA, and its structure diagram is shown in figure 1 shown. The human albumin signal peptide coding sequence is shown in SEQ ID NO.1, and the human albumin mature peptide coding sequence is shown in SEQ ID NO.4.

Embodiment 2

[0135] Example 2 Construction of Engineering Bacteria Co-expressing Yeast Protein Disulfide Bond Isomerase

[0136] Recombinant Engineering Bacteria II

[0137] Respectively pPicZA-PDI (structural schematic diagram as figure 2 shown) and pPic9-HSA plasmid were recombined into the KM71 cell genome twice, the human albumin signal peptide coding sequence is shown in SEQ ID NO.1, and the human albumin mature peptide coding sequence is shown in SEQ ID NO.3. The signal peptide coding sequence of yeast protein disulfide bond isomerase is shown in SEQ ID NO.6, and the mature peptide coding sequence is shown in SEQ ID NO.7.

[0138] Recombinant Engineering Bacteria III

[0139] Respectively pPic9-HSA-PDI (structural schematic diagram as image 3 shown) and pPicZA-HSA-PDI (structural schematic diagram as Figure 4 Shown) the plasmid was recombined into the KM71 cell genome twice, the human albumin signal peptide coding sequence is shown in SEQ ID NO.1, and the human albumin mature ...

Embodiment 3

[0140] Example 3 Construction of Engineering Bacteria Co-expressing Human Protein Disulfide Bond Isomerase

[0141] Recombinant Engineering Bacteria IV

[0142] The pPicZA-PDI and pPic9-HSA plasmids were recombined into the KM71 cell genome twice, the human albumin signal peptide coding sequence is shown in SEQ ID NO.1, and the human albumin mature peptide coding sequence is shown in SEQ ID NO.3. Show. The signal peptide coding sequence of human protein disulfide bond isomerase is shown in SEQ ID NO.9, and the mature peptide coding sequence is shown in SEQ ID NO.11.

[0143] Recombinant engineered bacteria V

[0144] The transformed recombinant plasmid is pPic9-HSA-PDI, and the structure diagram is as follows image 3 shown. The human albumin signal peptide coding sequence is shown in SEQ ID NO.1, and the human albumin mature peptide coding sequence is shown in SEQ ID NO.3. The signal peptide coding sequence of human protein disulfide bond isomerase is shown in SEQ ID NO....

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Abstract

The present invention relates to the field of genes, and particularly relates to a method for improving the recombinant human albumin expression quality and reducing degradation and an application. The present invention relates to the method for improving the recombinant human albumin expression quality and reducing the degradation. By over-expressing protein disulfide isomerase (PDI) in recombinant host cells, wrong shear in a protein secretion pathway is reduced, protein degradation is reduced, and the quality of exogenous protein expression is improved.

Description

technical field [0001] The invention relates to the field of genes, in particular to a method and application for improving the expression quality of recombinant human albumin and reducing degradation. Background technique [0002] The yeast expression system has the advantages of high fermentation density, strong secretion ability, and low degree of glycosylation, but the expression of foreign protein is also accompanied by the expression of a certain amount of protease, so that the expressed foreign protein is degraded to varying degrees. It directly affects the subsequent purification work and the quality of the recombinant protein. [0003] Yeast cells contain secretory pathway proteases (kex2 protease, Yap3 protease) and vacuolar proteases (protease A, protease B, carboxypeptidase Y). The foreign protein polypeptide chain is synthesized in the ribosome, then enters the endoplasmic reticulum to be folded under the traction of the signal peptide, and after being processe...

Claims

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Application Information

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IPC IPC(8): C12N1/19C12N15/81C12N15/14C12N15/61C12R1/84C12R1/78C12R1/72
CPCC07K14/765C12N9/90C12N15/815C12Y503/04001
Inventor 项炜韩旭姜钧茹
Owner TONGHUA ANRATE BIOPHARMACEUTICAL CO LTD
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