HIV-1 is dependent on its immature lattice to recruit IP6 for mature capsid assembly

被引:18
|
作者
Renner, Nadine [1 ]
Kleinpeter, Alex [2 ]
Mallery, Donna L. [1 ]
Albecka, Anna [1 ]
Faysal, Rifat K. M. [3 ,4 ]
Bocking, Till [3 ,4 ]
Saiardi, Adolfo [5 ]
Freed, Eric O. [2 ]
James, Leo C. [1 ]
机构
[1] MRC Lab Mol Biol, Francis Crick Ave, Cambridge, England
[2] NCI, Virus Cell Interact Sect, HIV Dynam & Replicat Program, Ctr Canc Res, Frederick, MD 21701 USA
[3] UNSW Sydney, Sch Med Sci, EMBL Australia Node Single Mol Sci, Sydney, NSW, Australia
[4] UNSW Sydney, Sch Med Sci, ARC Ctr Excellence Adv Mol Imaging, Sydney, NSW, Australia
[5] UCL, MRC Lab Mol Cell Biol, London, England
基金
英国惠康基金; 英国医学研究理事会; 澳大利亚国家健康与医学研究理事会; 美国国家卫生研究院;
关键词
D O I
10.1038/s41594-022-00887-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
HIV-1 Gag metamorphoses inside each virion, from an immature lattice that forms during viral production to a mature capsid that drives infection. Here we show that the immature lattice is required to concentrate the cellular metabolite inositol hexakisphosphate (IP6) into virions to catalyze mature capsid assembly. Disabling the ability of HIV-1 to enrich IP6 does not prevent immature lattice formation or production of the virus. However, without sufficient IP6 molecules inside each virion, HIV-1 can no longer build a stable capsid and fails to become infectious. IP6 cannot be replaced by other inositol phosphate (IP) molecules, as substitution with other IPs profoundly slows mature assembly kinetics and results in virions with gross morphological defects. Our results demonstrate that while HIV-1 can become independent of IP6 for immature assembly, it remains dependent upon the metabolite for mature capsid formation.
引用
收藏
页码:370 / 382
页数:30
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