Development of a functional monoclonal single-chain variable fragment antibody against Venezuelan equine encephalitis virus

被引:10
|
作者
Alvi, AZ
Stadnyk, LL
Nagata, LP
Fulton, RE [1 ]
Bader, DE
Roehrig, JT
Suresh, MR
机构
[1] Univ Alberta, Fac Pharm & Pharmaceut Sci, Edmonton, AB, Canada
[2] Def Res Estab Suffield, Hazard Avoidance Sect, Ralston, AB, Canada
[3] Def Res Estab Suffield, Med Countermeasure Sect, Ralston, AB, Canada
[4] Ctr Dis Control & Prevent, Arbovirus Dis Branch, Div Vector Borne Infect Dis, Natl Ctr Infect Dis,US Publ Hlth Serv,Dept Hlth &, Fort Collins, CO USA
来源
HYBRIDOMA | 1999年 / 18卷 / 05期
关键词
D O I
10.1089/hyb.1999.18.413
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We have generated a single-chain variable fragment (ScFv) antibody, from a previously well-characterized monoclonal antibody (MAb) to Venezuelan equine encephalitis (VEE) virus, 5B4D-6, The variable regions of the heavy (VH) and light (VL) chain antibody genes, were connected by a DNA linker and cloned in the phagemid vector pCANTAB5E, The ScFv clone in Escherichia coli strain TG-1, 5B4D-6-6, was expressed as a similar to 30 kDa ScFv protein and higher molecular weight fusion products which were functional in recognizing VEE virus by enzyme-linked immunosorbent assay (ELISA), Results were reproduced in Escherichia coli strain HB2151, where clone D66 was expressed mainly as soluble periplasmic protein. The D66 ScFv antibody bound VEE virus strongly as determined by ELISA, Nucleotide sequence analysis of 5B4D-6-6 ScFv indicated that the V-kappa gene belonged to family XVI, subgroup V, while the V-H gene was unique in its sequence, though its amino acid sequence could be subgrouped as IA, The deduced protein sequence of D66 was highly homologous to published murine ScFv protein sequences. This work demonstrates, for the first time, cloning of a functional ScFv antibody against VEE virus.
引用
收藏
页码:413 / 421
页数:9
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