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

机译:与三种主要灵长类慢病毒谱系交叉反应的单克隆抗衣壳抗体的表征

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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.
机译:通过用完全灭活的SIVagmTYO-1免疫小鼠,产生了针对猿猴和人类免疫缺陷病毒(SIV / HIV)Gag衣壳的特异性不同的小鼠单克隆抗体。单克隆抗体AG3.0表现出最广泛的反应性,可识别HIV-1,HIV-2,SIVmac和SIVagm的Gag衣壳蛋白(p24-27)和Gag前体p38,p55和p150。使用重叠的肽,将AG3.0表位在衣壳中定位到在HIV-1,HIV-2,SIVrcm,SIVsm / mac和SIVagm相关病毒中保守的序列(SPRTLNA)。由于其广泛的交叉反应性,AG3.0被用于开发具有较低检测限100. pg / ml HIV-1 Gag p24的抗原捕获测定法。有趣的是,发现AG3.0的SIVagmVer和SIVmac Gag的结合开/关速率比SIVagmSab Gag快,这可能是由于SPRTLNA基序以外的差异所致。此外,对编码AG3.0的核糖核酸(RNA)进行了测序,以促进人源化单克隆抗体的开发。

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