Structural Studies of Alix and ESCRT Complexes in HIV-1 Budding

HIV-1 出芽中 Alix 和 ESCRT 复合物的结构研究

• 批准号: 8148741
• 负责人: James Hurley
• 金额: $ 36.33万
• 依托单位: NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES
• 依托单位国家: 美国
• 资助国家: 美国
• 起止时间: 至
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/8148741
• 关键词: Complex; HIV-1

Structural Studies of Alix and ESCRT Complexes in HIV-1 Budding HIV-1 particle assembly and release depend on a protein network that includes Alix and Vps4A/B, and four multiprotein complexes: Hrs/STAM and ESCRT-I, II, and III. These proteins and complexes are conserved from yeast to human, and their normal function is to sort monoubiquitinated receptors, enzymes, and other cargo to the lysosome or vacuole. Inactivation of any one of several proteins tested in this network blocks HIV release and infectivity. The objectives of this projects are to 1) map the molecular interactions between HIV and ESCRT components at the level of individual protein domains; 2) characterize the binding affinities and relevant structures of the components involved in these interactions; and 3) in collaboration with Eric Freed, NCI, to design means for inhibiting HIV-1 budding from cells.

HIV-1 出芽中 Alix 和 ESCRT 复合物的结构研究 HIV-1 颗粒的组装和释放取决于包括 Alix 和 Vps4A/B 以及四种多蛋白复合物的蛋白质网络：Hrs/STAM 和 ESCRT-I、II 和 III。这些蛋白质和复合物从酵母到人类都是保守的，它们的正常功能是将单泛素化受体、酶和其他货物分选到溶酶体或液泡。该网络中测试的几种蛋白质中任何一种的失活都会阻止艾滋病毒的释放和传染性。该项目的目标是 1) 在单个蛋白质结构域水平上绘制 HIV 和 ESCRT 成分之间的分子相互作用； 2）表征这些相互作用所涉及的组分的结合亲和力和相关结构； 3) 与NCI的Eric Freed合作，设计抑制细胞中HIV-1出芽的方法。