Characterization of a monoclonal anti-capsid antibody that cross-reacts with three major primate lentivirus lineages

被引:9
|
作者
Sanders-Beer, Brigitte E. [1 ]
Eschricht, Magdalena [2 ]
Seifried, Janna [2 ]
Hirsch, Vanessa M. [3 ]
Allan, Jonathan S. [4 ]
Norley, Stephen [2 ]
机构
[1] BIOQUAL Inc, Rockville, MD 20850 USA
[2] Robert Koch Inst, D-13353 Berlin, Germany
[3] NIAID, Mol Microbiol Lab, NIH, Bethesda, MD 20892 USA
[4] Texas Biomed Res Inst, Dept Virol & Immunol, San Antonio, TX 78227 USA
关键词
AG3.0; Epitope; Gag; Capsid; p24; p27; Human immunodeficiency virus; Simian immunodeficiency virus; SIMIAN-IMMUNODEFICIENCY-VIRUS; AFRICAN-GREEN MONKEYS; COLOBUS PILIOCOLOBUS-BADIUS; DEFICIENCY SYNDROME AIDS; GAG PROTEIN; MOLECULAR CHARACTERIZATION; GENETIC DIVERSITY; CYCLOPHILIN-A; CAPTURE ASSAY; POSTTRANSLATIONAL MODIFICATIONS;
D O I
10.1016/j.virol.2011.11.003
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Mouse monoclonal antibodies with varying specificities against the Gag capsid of simian and human immunodeficiency virus (SIV/HIV) were generated by immunizing mice with whole inactivated SIVagmTYO-1. Monoclonal antibody AG3.0 showed the broadest reactivity recognizing the Gag capsid protein (p24-27) and Gag precursors p38, p55, and p150 of HIV-1, HIV-2, SIVmac, and SIVagm. Using overlapping peptides, the AG3.0 epitope was mapped in capsid to a sequence (SPRTLNA) conserved among HIV-1, HIV-2, SIVrcm, SIVsm/mac, and SIVagm related viruses. Because of its broad cross-reactivity, AG3.0 was used to develop an antigen capture assay with a lower detection limit of 100 pg/ml HIV-1 Gag p24. Interestingly, AG3.0 was found to have a faster binding on/off rate for SIVagmVer and SIVmac Gag than for SIVagmSab Gag, possibly due to differences outside the SPRTLNA motif. In addition, the ribonucleic acid (RNA) coding for AG3.0 was sequenced to facilitate the development of humanized monoclonal antibodies. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:402 / 412
页数:11
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