Mateu Mauricio G
Centro de Biología Molecular 'Severo Ochoa' (CSIC-UAM), Universidad Autónoma de Madrid, Cantoblanco, 28049 Madrid, Spain.
FEBS J. 2009 Nov;276(21):6098-109. doi: 10.1111/j.1742-4658.2009.07313.x.
The capsid protein (CA) of HIV-1 is composed of two domains, the N-terminal domain (NTD) and the C-terminal domain (CTD). During the assembly of the immature HIV-1 particle, both CA domains constitute a part of the Gag polyprotein, which forms a spherical capsid comprising up to 5000 radially arranged, extended subunits. Gag-Gag interactions in the immature capsid are mediated in large part by interactions between CA domains, which are involved in the formation of a lattice of connected Gag hexamers. After Gag proteolysis during virus maturation, the CA protein is released, and approximately 1000-1500 free CA subunits self-assemble into a truncated cone-shaped capsid. In the mature capsid, NTD-NTD and NTD-CTD interfaces are involved in the formation of CA hexamers, and CTD-CTD interfaces connect neighboring hexamers through homodimerization. The CA-CA interfaces involved in the assembly of the immature capsid and those forming the mature capsid are different, at least in part. CA appears to have evolved an extraordinary conformational plasticity, which allows the creation of multiple CA-CA interfaces and the occurrence of CA conformational switches. This minireview focuses on recent structure-function studies of the diverse CA-CA interactions and interfaces involved in HIV-1 assembly. Those studies are leading to a better understanding of molecular recognition events during virus morphogenesis, and are also relevant for the development of anti-HIV drugs that are able to interfere with capsid assembly or disassembly.
人类免疫缺陷病毒1型(HIV-1)的衣壳蛋白(CA)由两个结构域组成,即N端结构域(NTD)和C端结构域(CTD)。在未成熟HIV-1颗粒组装过程中,两个CA结构域均构成Gag多聚蛋白的一部分,该多聚蛋白形成一个球形衣壳,包含多达5000个呈放射状排列的伸展亚基。未成熟衣壳中的Gag-Gag相互作用在很大程度上由CA结构域之间的相互作用介导,这些相互作用参与形成连接的Gag六聚体晶格。在病毒成熟过程中Gag蛋白水解后,CA蛋白被释放,约1000 - 1500个游离的CA亚基自组装成一个截顶圆锥形衣壳。在成熟衣壳中,NTD-NTD和NTD-CTD界面参与CA六聚体的形成,CTD-CTD界面通过同二聚化连接相邻的六聚体。参与未成熟衣壳组装的CA-CA界面与形成成熟衣壳的界面至少部分不同。CA似乎进化出了非凡的构象可塑性,这使得能够形成多个CA-CA界面并发生CA构象转换。本综述聚焦于近期关于HIV-1组装中多种CA-CA相互作用和界面的结构-功能研究。这些研究有助于更好地理解病毒形态发生过程中的分子识别事件,也与能够干扰衣壳组装或拆卸的抗HIV药物的开发相关。