2006•Huadong Li-Gong Daxue xuebaoRequires access

Construction of Phage-scFv and Soluble scFv against Foot and Mouth Disease Virus

Cao Sheng-feng, Guofeng Wang

Open publisher page 0 citations

Abstract

The anti-foot-and-mouth disease virus(FMDV) single-chain Fv(scFv) gene was constructed by DNA recombinant technology.The 1C7V_H and V_L genes were assembled into scFv gene with a linker sequence(Gly_4Ser)_3 by splicing overlop extension and scFv gene was amplified by PCR.The scFv gene was subcloned into phagemid vector pCANTAB 5E.The phage scFv displaying library was constructed by male Escherichia coli TG1 transfected with resultant phagemid pCANTAB 5E-scFv.The scFv positive clone was obtained after the phage scFv displaying library was rescued by M13KO7 and biopanned with FMDV antigen for 3 rounds.Escherichia coli BH2151 was transfected with the positive clone and scFv protein was expressed by Escherichia coli BH2151 through the inducement of IPTG.The results of ELISA show that phage-scFv and soluble scFv,which were expressed by the selected scFv gene,have high affinity and specificity to FMDV.

About this research paper

What this paper is about

The anti-foot-and-mouth disease virus(FMDV) single-chain Fv(scFv) gene was constructed by DNA recombinant technology.The 1C7V_H and V_L genes were assembled into scFv gene with a linker sequence(Gly_4Ser)_3 by splicing overlop extension and scFv gene was amplified by PCR.The scFv gene was subcloned into phagemid vector pCANTAB 5E.The phage scFv displaying library was constructed by male Escherichia coli TG1 transfected with resultant phagemid pCANTAB 5E-scFv.The scFv positive clone was obtained after the phage scFv displaying library was rescued by M13KO7 and biopanned with FMDV antigen for 3 rounds.Escherichia coli BH2151 was transfected with the positive clone and scFv protein was expressed by Escherichia coli BH2151 through the inducement of IPTG.The results of ELISA show that phage-scFv and soluble scFv,which were expressed by the selected scFv gene,have high affinity and specificity to FMDV.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

The anti-foot-and-mouth disease virus(FMDV) single-chain Fv(scFv) gene was constructed by DNA recombinant technology.The 1C7V_H and V_L genes were assembled into scFv gene with a linker sequence(Gly_4Ser)_3 by splicing overlop extension and scFv gene was amplified by PCR.The scFv gene was subcloned into phagemid vector pCANTAB 5E.The phage scFv displaying library was constructed by male Escherichia coli TG1 transfected with resultant phagemid pCANTAB 5E-scFv.The scFv positive clone was obtained after the phage scFv displaying library was rescued by M13KO7 and biopanned with FMDV antigen for 3 rounds.Escherichia coli BH2151 was transfected with the positive clone and scFv protein was expressed by Escherichia coli BH2151 through the inducement of IPTG.The results of ELISA show that phage-scFv and soluble scFv,which were expressed by the selected scFv gene,have high affinity and specificity to FMDV.

Key concepts: Phagemid, Escherichia coli, Phage display, Molecular biology, Recombinant DNA, Gene, Virology, Biology

Related papers

Back to paper searchBrowse research topicsOriginal source
Construction of Phage-scFv and Soluble scFv against Foot and Mouth Disease Virus — Research Paper | ScholarLens