Cloning of the variable region genes from hybridoma against HAAH and then construction and expression of anti-HAAH scFv

AIM: Construction and expression of anti-HAAH single chain variable fragment (scFv) by cloning of the variable region genes from anti-HAAH hybridoma cells G3/F11. METHODS: Total RNA was extracted from hybridoma cells G3/F11. By RT-PCR, murine V(H) and V(L) genes of mAb were amplified respectively. Then, They were assembled into V(H)-linker-V(L) scFv template by SOE-PCR and anti-HAAH scFv was express in E.coli by constructed pHEN 1-anti-HAAH vector. The expression of anti-HAAH scFv were detected by SDS-PAGE and Western blotting and the binding activity were demonstrated by ELISA. RESULTS: The analysis of DNA sequencing shown that the full-length of constructed scFv gene was 744 bp, encoding 248 amino acids. Moreover, the V(H) and V(L) genes were functional antibody variable region genes, as there were four FRs and three CDRs in both of them. By SDS-PAGE and Western blotting, the expression level of anti-HAAH scFv were detected. The expression level of pHEN 1-anti-HAAH scFv, which was expressed in E.coli HB2151, was 7.8% in total E.coli protein and were existed in soluble protein mainly. By indirect ELISA detection with HAAH protein, the binding activity of soluble anti-HAAH scFv was very well. CONCLUSION: The murine V(H) and V(L) genes of mAb against HAAH have been cloned successfully and anti-HAAH scFv have been constructed and expressed. Besides, the scFv could be further studied about their biological activity and application, due to their high affinity shown in preliminary detection.