2010•PubMedRequires access

[Expression of human TFF3 in Escherichia coli].

Rui Lu, Xin Wang, Jianping Chen, Xian Chen, Jia-nan Xu

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Abstract

OBJECTIVE: To construct recombinant human TFF3 prokaryotic expressing plasmid, express it in E. coli and identify the expressed protein. METHODS: The cDNA for mature peptide of TFF3 was amplified by RT-PCR from RNA of human colon tissue and inserted into the MCS of the prokaryotic expressing plasmid pET32a (+). Then TFF3 was expressed as a fusion protein by IPTG induction. The recombinant protein was determined by SDS-PAGE and Western blot with a rabbit anti-TFF3 polyclonal antibody. RESULTS: Sequencing result indicated that the obtained TFF3 fragment was inserted into plasmid pET32a (+) successfully and the sequence was correct. The expression level of the fusion protein was highest after 6h induction with 1 mmol/L IPTG. The result of Western blot demonstrated that the relative molecular mass of recombinant protein was about 24 x 10(3) and the protein had good antigenicity and specificity. CONCLUSION: The expression plasmid pET32a-TFF3 was constructed and expressed successfully. This study will provide a substantial basis for further study of human TFF3.

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OBJECTIVE: To construct recombinant human TFF3 prokaryotic expressing plasmid, express it in E. coli and identify the expressed protein. METHODS: The cDNA for mature peptide of TFF3 was amplified by RT-PCR from RNA of human colon tissue and inserted into the MCS of the prokaryotic expressing plasmid pET32a (+). Then TFF3 was expressed as a fusion protein by IPTG induction. The recombinant protein was determined by SDS-PAGE and Western blot with a rabbit anti-TFF3 polyclonal antibody. RESULTS: Sequencing result indicated that the obtained TFF3 fragment was inserted into plasmid pET32a (+) successfully and the sequence was correct. The expression level of the fusion protein was highest after 6h induction with 1 mmol/L IPTG. The result of Western blot demonstrated that the relative molecular mass of recombinant protein was about 24 x 10(3) and the protein had good antigenicity and specificity. CONCLUSION: The expression plasmid pET32a-TFF3 was constructed and expressed successfully. This study will provide a substantial basis for further study of human TFF3.

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Available abstract

OBJECTIVE: To construct recombinant human TFF3 prokaryotic expressing plasmid, express it in E. coli and identify the expressed protein. METHODS: The cDNA for mature peptide of TFF3 was amplified by RT-PCR from RNA of human colon tissue and inserted into the MCS of the prokaryotic expressing plasmid pET32a (+). Then TFF3 was expressed as a fusion protein by IPTG induction. The recombinant protein was determined by SDS-PAGE and Western blot with a rabbit anti-TFF3 polyclonal antibody. RESULTS: Sequencing result indicated that the obtained TFF3 fragment was inserted into plasmid pET32a (+) successfully and the sequence was correct. The expression level of the fusion protein was highest after 6h induction with 1 mmol/L IPTG. The result of Western blot demonstrated that the relative molecular mass of recombinant protein was about 24 x 10(3) and the protein had good antigenicity and specificity. CONCLUSION: The expression plasmid pET32a-TFF3 was constructed and expressed successfully. This study will provide a substantial basis for further study of human TFF3.

Key concepts: Recombinant DNA, Fusion protein, Antigenicity, Plasmid, Molecular biology, Polyclonal antibodies, Complementary DNA, lac operon

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