Search for Molecules against HIV-CA
宮﨑, 恭行 Tokyo Metropolitan Institute of Medical Science KAKEN研究者をさがす
土肥, 直哉 Tokushima University 徳島大学 教育研究者総覧
駒, 貴明 Tokushima University 徳島大学 教育研究者総覧 KAKEN研究者をさがす
足立, 昭夫 Tokushima University|Kansai Medical University 徳島大学 教育研究者総覧 KAKEN研究者をさがす
野間口, 雅子 Tokushima University 徳島大学 教育研究者総覧 KAKEN研究者をさがす
Varieties of in vitro systems have been used to study biochemical properties of human immunodeficiency virus Gag-capsid protein (HIV Gag-CA). Recently, we have comparatively characterized HIV-1 and HIV-2 Gag-CA proteins using such technology, and have demonstrated that the NaCl-initiated CA-polymerization in vitro and the stability of CA N-terminal domain as judged by differential scanning fluorimetry (DSF) are inversely correlated. In this study, we found that ZnCl2 works as a competent initiator of the in vitro HIV-1 CA-polymerization at much lower concentrations than those of NaCl frequently used for the polymerization initiation. We also showed by DSF assays that ZnCl2 highly destabilize HIV-1 CA. Furthermore, PF74, a well-known inducer of premature HIV-1 uncoating in infected cells, was demonstrated to unusually promote the HIV-1 CA-disassembly in the presence of ZnCl2 as revealed by DSF assays. Taken together, we conclude that the DSF method may be useful as an efficient monitoring system to screen anti-HIV-1 CA molecules.
Frontiers in Microbiology
Frontiers Media S.A.
Copyright © 2017 Miyazaki, Doi, Koma, Adachi and Nomaguchi. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). (https://creativecommons.org/licenses/by/4.0/) The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
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