1Institute for Molecular Virology, University of Minnesota Minneapolis, MN, USA ; 2Department of Diagnostic and Biological Sciences, School of Dentistry, University of Minnesota , Minneapolis, MN, USA.
1Institute for Molecular Virology, University of Minnesota Minneapolis, MN, USA ; 3Pharmacology Graduate Program, University of Minnesota Minneapolis, MN, USA.
Front Microbiol. 2014 Jun 24;5:302. doi: 10.3389/fmicb.2014.00302. eCollection 2014.
A critical aspect of viral replication is the assembly of virus particles, which are subsequently released as progeny virus. While a great deal of attention has been focused on better understanding this phase of the viral life cycle, many aspects of the molecular details remain poorly understood. This is certainly true for retroviruses, including that of the human immunodeficiency virus type 1 (HIV-1; a lentivirus) as well as for human T-cell leukemia virus type 1 (HTLV-1; a deltaretrovirus). This review discusses the retroviral Gag protein and its interactions with itself, the plasma membrane and the role of lipids in targeting Gag to virus assembly sites. Recent progress using sophisticated biophysical approaches to investigate - in a comparative manner - retroviral Gag-Gag and Gag-membrane interactions are discussed. Differences among retroviruses in Gag-Gag and Gag-membrane interactions imply dissimilar molecular aspects of the viral assembly pathway, including the interactions of Gag with lipids at the membrane.
病毒复制的一个关键方面是病毒粒子的组装,随后这些病毒粒子作为子代病毒释放。尽管人们已经非常关注更好地理解病毒生命周期的这一阶段,但分子细节的许多方面仍然知之甚少。这对于逆转录病毒来说确实如此,包括人类免疫缺陷病毒 1 型(HIV-1;慢病毒)和人类 T 细胞白血病病毒 1 型(HTLV-1;δ逆转录病毒)。本文综述了逆转录病毒 Gag 蛋白及其与自身、质膜的相互作用,以及脂质在将 Gag 靶向病毒组装部位中的作用。本文还讨论了使用复杂的生物物理方法在比较的基础上研究逆转录病毒 Gag-Gag 和 Gag-膜相互作用的最新进展。逆转录病毒之间在 Gag-Gag 和 Gag-膜相互作用方面的差异意味着病毒组装途径的分子方面存在差异,包括 Gag 与膜上脂质的相互作用。