Suppr超能文献

HIV-1 Vpr-氯霉素乙酰转移酶融合蛋白:病毒体整合的序列要求及抗病毒效果分析

HIV-1 Vpr-chloramphenicol acetyltransferase fusion proteins: sequence requirement for virion incorporation and analysis of antiviral effect.

作者信息

Yao X J, Kobinger G, Dandache S, Rougeau N, Cohen E

机构信息

Laboratoire de Rétrovirologie Humaine, Département de Microbiologie et Immunologie, Faculté de Médecine, Université de Montréal, CP 6128, Succursale Centre-ville, Montréal, Québec H3C 3J7 Canada.

出版信息

Gene Ther. 1999 Sep;6(9):1590-9. doi: 10.1038/sj.gt.3300988.

Abstract

The human immunodeficiency virus type 1 Vpr is a virion-associated protein that is incorporated in trans into viral particles, presumably via an interaction with the p6 domain of the Gag polyprotein precursor. Recently, several studies demonstrated that Vpr fusion proteins could be used as intravirion inactivating agents. In this study, we compared different Vpr-chloramphenicol acetyltransferase (CAT) fusion proteins for their virion incorporation ability and their effect on the infectivity of HIV viruses. Our deletion analysis indicates that both the N-terminal alpha-helical domain and the leucine/isoleucine-rich (LR) domain located in the middle region of Vpr are required for optimal virion incorporation of Vpr-CAT fusion proteins. The C-terminal basic region, associated with Vpr's ability to mediate cell cycle arrest in G2, was not required for virion incorporation, thus allowing the development of Vpr-based chimeric proteins devoid of any effect on cell growth. The fusion of Vpr at the N- or C-terminus of CAT targeted with equal efficiency the chimeric protein into virions. While the virion incorporation of most Vpr-CAT fusion proteins tested in this study was dependent on the presence of an intact p6 domain, fusion proteins containing only the N-terminal alpha-helical domain of Vpr (amino acid 1 to 42) were incorporated into virions in a p6-independent manner. Virion incorporation of Vpr-CAT fusion proteins was shown to decrease viral infectivity. Moreover, the insertion of HIV protease-cleavage sites between Vpr and CAT not only efficiently delivered and released the cleaved CAT product into HIV viral particles, but also greatly potentiated the inhibition of progeny virion infectivity. Overall, our study: (1) defines the Vpr sequence requirement and configuration necessary for the specific and optimal incorporation of Vpr fusion protein into HIV particles; (2) shows that Vpr fusion proteins have the ability to suppress HIV infectivity by targeting multiple steps of viral morphogenesis.

摘要

人类免疫缺陷病毒1型Vpr是一种与病毒粒子相关的蛋白质,可能通过与Gag多蛋白前体的p6结构域相互作用而反式掺入病毒粒子中。最近,多项研究表明Vpr融合蛋白可用作病毒粒子内的失活剂。在本研究中,我们比较了不同的Vpr-氯霉素乙酰转移酶(CAT)融合蛋白的病毒粒子掺入能力及其对HIV病毒感染性的影响。我们的缺失分析表明,Vpr-CAT融合蛋白最佳地掺入病毒粒子需要位于Vpr中间区域的N端α螺旋结构域和富含亮氨酸/异亮氨酸(LR)的结构域。与Vpr介导细胞周期停滞在G2期的能力相关的C端碱性区域对于病毒粒子掺入不是必需的,因此允许开发对细胞生长没有任何影响的基于Vpr的嵌合蛋白。Vpr在CAT的N端或C端融合能以相同效率将嵌合蛋白靶向到病毒粒子中。虽然本研究中测试的大多数Vpr-CAT融合蛋白的病毒粒子掺入依赖于完整p6结构域的存在,但仅包含Vpr的N端α螺旋结构域(氨基酸1至42)的融合蛋白以不依赖p6的方式掺入病毒粒子中。已表明Vpr-CAT融合蛋白的病毒粒子掺入降低了病毒感染性。此外,在Vpr和CAT之间插入HIV蛋白酶切割位点不仅有效地将切割后的CAT产物递送至HIV病毒粒子并释放出来,而且还大大增强了对子代病毒粒子感染性的抑制作用。总体而言,我们的研究:(1)确定了Vpr融合蛋白特异性和最佳地掺入HIV颗粒所需的Vpr序列要求和构型;(2)表明Vpr融合蛋白有能力通过靶向病毒形态发生的多个步骤来抑制HIV感染性。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验