衣壳
格子(音乐)
群体特异性抗原
生物物理学
化学
蛋白酶
细胞生物学
曲率
物理
膜
结晶学
血浆蛋白结合
病毒复制
分子
生物
蛋白质结构
病毒学
膜曲率
病毒
分子生物物理学
晶体结构
多聚蛋白质类
作者
Benjamin Preece,Wiley Peppel,Haley Durden,Rodrigo Gallegos,Gabriel Clinger,Nicole Bohn,Antje Huwendiek-Poser,Gillian Ysassi,Allyson Roman,Giovanna Garcia,Tasheena Cly,David Belnap,Saveez Saffarian
出处
期刊:
[Cold Spring Harbor Laboratory]
日期:2025-12-09
标识
DOI:10.64898/2025.12.08.693107
摘要
HIV-1 is released from infected cells as immature virions whose membranes are supported by a Gag lattice. During maturation, this lattice is cleaved by the viral protease to release capsid proteins that assemble into the mature core. The architecture of the Gag lattice is central to this process, and the Gag lattice is targeted by maturation inhibitors that block cleavage. Using cryo-electron tomography, we compared Gag-only virus-like particles (VLPs) with immature HIV-1 virions and found that VLPs assemble denser and more complete lattices, exhibiting a strong correlation between lattice curvature and Gag copy number. In contrast, immature virions incorporate fewer Gag molecules and display weaker coupling between curvature and Gag stoichiometry. These findings show that while Gag alone can form the canonical immature lattice, additional viral components fine-tune lattice organization and curvature, potentially regulating protease accessibility, virion release, and the onset of HIV-1 maturation.
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