González María Eugenia
Unidad de Expresión Viral, Centro Nacional de Microbiología, Instituto de Salud Carlos III, Carretera de Majadahonda-Pozuelo Km 2, Majadahonda, 28220 Madrid, Spain.
Int J Mol Sci. 2017 Jan 10;18(1):126. doi: 10.3390/ijms18010126.
The human immunodeficiency virus type 1 (HIV-1) Vpr protein is an attractive target for antiretroviral drug development. The conservation both of the structure along virus evolution and the amino acid sequence in viral isolates from patients underlines the importance of Vpr for the establishment and progression of HIV-1 disease. While its contribution to virus replication in dividing and non-dividing cells and to the pathogenesis of HIV-1 in many different cell types, both extracellular and intracellular forms, have been extensively studied, its precise mechanism of action nevertheless remains enigmatic. The present review discusses how the apparently multifaceted interplay between Vpr and host cells may be due to the impairment of basic metabolic pathways. Vpr protein modifies host cell energy metabolism, oxidative status, and proteasome function, all of which are likely conditioned by the concentration and multimerization of the protein. The characterization of Vpr domains along with new laboratory tools for the assessment of their function has become increasingly relevant in recent years. With these advances, it is conceivable that drug discovery efforts involving Vpr-targeted antiretrovirals will experience substantial growth in the coming years.
人类免疫缺陷病毒1型(HIV-1)的Vpr蛋白是抗逆转录病毒药物研发的一个有吸引力的靶点。病毒进化过程中结构的保守性以及患者病毒分离株中氨基酸序列的保守性都突显了Vpr对于HIV-1疾病发生和发展的重要性。虽然其在分裂细胞和非分裂细胞中对病毒复制的作用以及在许多不同细胞类型(包括细胞外和细胞内形式)中对HIV-1发病机制的作用已得到广泛研究,但其确切作用机制仍然成谜。本综述讨论了Vpr与宿主细胞之间明显多方面的相互作用可能是由于基本代谢途径受损所致。Vpr蛋白会改变宿主细胞的能量代谢、氧化状态和蛋白酶体功能,所有这些可能都受该蛋白浓度和多聚化的影响。近年来,Vpr结构域的表征以及用于评估其功能的新实验室工具变得越来越重要。随着这些进展,可以想象在未来几年,针对Vpr的抗逆转录病毒药物的研发工作将大幅增加。