探索 HIV-1 成熟:抗病毒开发的新前沿

Viruses Pub Date : 2024-09-06 DOI:10.3390/v16091423
Aidan McGraw, Grace Hillmer, Stefania M. Medehincu, Yuta Hikichi, Sophia Gagliardi, Kedhar Narayan, Hasset Tibebe, Dacia Marquez, Lilia Mei Bose, Adleigh Keeting, Coco Izumi, Kevin Peese, Samit Joshi, Mark Krystal, Kathleen L. DeCicco-Skinner, Eric O. Freed, Luca Sardo, Taisuke Izumi
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摘要

HIV-1 病毒成熟是病毒复制周期中产生传染性病毒粒子的重要步骤。Gag 和 Gag-Pol 多聚蛋白在病毒产生细胞的质膜上组装,并从质膜上萌发到细胞外。新释放的后代病毒最初是不成熟的,没有感染性。然而,一旦后代病毒中的 Gag 多聚蛋白被病毒蛋白酶裂解,成熟的囊膜蛋白就会聚集形成富勒烯核心。该核心含有两份病毒基因组 RNA,可将病毒颗粒形态转变为具有传染性的病毒颗粒。这种形态转变被称为成熟。病毒成熟会影响 Env 糖蛋白在病毒表面的分布,并诱发随后与 CD4 受体相互作用所需的构象变化。一些宿主因素,包括环嗜蛋白 A 等蛋白质、IP6 等代谢物和含有鞘磷脂的脂筏,已被证明对病毒的成熟有影响。这篇综述文章深入探讨了病毒成熟和 Env 糖蛋白招募的过程,重点是宿主细胞因素和环境条件的作用。此外,我们还讨论了评估病毒成熟的显微技术,以及目前专门针对病毒复制中这一关键步骤的抗病毒药物的发展情况,从而提供长效治疗方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Exploring HIV-1 Maturation: A New Frontier in Antiviral Development
HIV-1 virion maturation is an essential step in the viral replication cycle to produce infectious virus particles. Gag and Gag-Pol polyproteins are assembled at the plasma membrane of the virus-producer cells and bud from it to the extracellular compartment. The newly released progeny virions are initially immature and noninfectious. However, once the Gag polyprotein is cleaved by the viral protease in progeny virions, the mature capsid proteins assemble to form the fullerene core. This core, harboring two copies of viral genomic RNA, transforms the virion morphology into infectious virus particles. This morphological transformation is referred to as maturation. Virion maturation influences the distribution of the Env glycoprotein on the virion surface and induces conformational changes necessary for the subsequent interaction with the CD4 receptor. Several host factors, including proteins like cyclophilin A, metabolites such as IP6, and lipid rafts containing sphingomyelins, have been demonstrated to have an influence on virion maturation. This review article delves into the processes of virus maturation and Env glycoprotein recruitment, with an emphasis on the role of host cell factors and environmental conditions. Additionally, we discuss microscopic technologies for assessing virion maturation and the development of current antivirals specifically targeting this critical step in viral replication, offering long-acting therapeutic options.
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