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Preparation method and application of recombinant protein A gene and expression product thereof

A recombinant protein and gene technology, applied in the biological field, can solve the problems of low affinity and low purification efficiency, and achieve the effects of high affinity, high expression efficiency and easy purification.

Active Publication Date: 2011-01-05
上海晟国医药发展有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

When using the affinity chromatography technology containing proteinA, there are problems such as low affinity and low purification efficiency. Therefore, when using the affinity chromatography technology, an improved ProteinA is needed to achieve higher affinity and improve the efficiency of purification. Effect

Method used

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  • Preparation method and application of recombinant protein A gene and expression product thereof
  • Preparation method and application of recombinant protein A gene and expression product thereof
  • Preparation method and application of recombinant protein A gene and expression product thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0027] Example 1 Synthesis of Recombinant Protein A Gene Monomer

[0028] By means of chemical synthesis, the sequence of a repetitive fragment of the recombinant protein A gene was designed and synthesized. The sequence included a length of 168 bp, and the NcoI restriction site connected to the expression vector was added to the front end, and 6 His (for affinity chromatography, and Nickel column combination, reducing purification steps) and EK restriction site, and AccI restriction site for ligation of multiple repeat fragments. In addition, it also includes the stop codon TAA, and a total of 9 bp of BamH I restriction endonuclease linker for cloning. It is also necessary to design and synthesize a sequence of a repeat segment of the recombinant protein A gene by chemical synthesis, which has a length of 168 bp and AccI restriction sites at both ends for constructing a sequence containing multiple repeat segments.

Embodiment 2

[0029] Example 2 Construction of a pET32a vector containing a recombinant protein A gene monomer

[0030] Cut out the above-mentioned recombinant protein A gene monomer with restriction endonucleases NcoI and BamHI, connect with the vector pET32a digested with NcoI and BamHI, transform Escherichia coli, screen the transformant with ampicillin resistance, and extract the plasmid , After identification by enzyme digestion, it was proved that the recombinant protein A gene monomer had been cloned into pET32a.

Embodiment 3

[0031] Example 3 Construction of pET32a-P vector containing recombinant protein A gene

[0032] The above pET32a vector containing a recombinant protein A gene monomer and the recombinant protein A gene monomer were digested with AccI, the corresponding fragments were recovered and ligated, transformed into Escherichia coli, and the transformants with ampicillin resistance were screened, extracted from the plasmid, and enzymatically The pET32a-P vector of recombinant protein A containing 3 protein A gene monomers was obtained by cleavage screening.

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Abstract

The invention provides a recombinant protein A gene with a nucleotide sequence expressed as SEQ ID No: 1 and recombinant protein A coded by the gene. The invention also provides a recombinant expression vector PET32a-P for expressing the recombinant protein A gene, escherichia coli BL21 / DE3 transformed by the recombinant expression vector and a method for preparing the recombinant protein A. The recombinant protein A provided by the invention is used for antibody detection, separation and purification, and the recombinant protein A and a chromatographic medium vector can form a compatible chromatographic medium. The recombinant protein A produced by the invention has the advantages of strong protein binding specificity, high affinity and great improvement on purification efficiency; and compared with the commercial ProteinA Sepharose 4Fast Flow, the recombinant protein A has obviously improved dynamic adsorption capacity.

Description

[0001] The present invention is a divisional application of the Chinese patent application with the title of the invention: a preparation method and application of a recombinant protein A gene and its expression product, and the application number is: 200710085148.X. technical field [0002] The invention belongs to the field of biotechnology, and specifically relates to a recombinant protein A gene, a carrier containing the recombinant gene, a transformed bacterial strain and a product expressed by the recombinant protein A gene, and a preparation method and application thereof. Background technique [0003] Staphylococcal Protein A (SPA) is a protein isolated from the cell wall of Staphylococcus aureus. In 1940, Vevwey found that some Staphylococcus aureus contained a substance that could form a precipitate with normal human serum in a two-way diffusion test. Jensen (1959) also discovered a similar phenomenon and named it the A antigen. [0004] In 1963, Lofkvist et al. i...

Claims

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Application Information

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IPC IPC(8): C12N15/31C12N15/70C07K14/31C07K1/22G01N33/53
Inventor 谈珉胡辉郭亚军
Owner 上海晟国医药发展有限公司
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