Nef increases the synthesis of and transports cholesterol to lipid rafts and HIV-1 progeny virions

被引:141
作者
Zheng, YH
Plemenitas, A
Fielding, CJ
Peterlin, BM [1 ]
机构
[1] Univ Calif San Francisco, Dept Med Microbiol & Immunol, Rosalind Russell Med Res Ctr, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Cardiovasc Res Inst, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Dept Physiol, San Francisco, CA 94143 USA
[4] Univ Ljubljana, Fac Med, Inst Biochem, SL-1000 Ljubljana, Slovenia
关键词
D O I
10.1073/pnas.1437453100
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
HIV buds from lipid rafts and requires cholesterol for its egress from and entry into cells. Viral accessory protein Nef plays a major role in this process. In this study, it not only increased the biosynthesis of lipid rafts and viral particles with newly synthesized cholesterol, but also enriched them. Furthermore, via the consensus cholesterol recognition motif at its C terminus, Nef bound cholesterol. When this sequence was mutated, Nef became unable to transport newly synthesized cholesterol into lipid rafts and viral particles. Interestingly, although its levels in lipid rafts were not affected, this mutant Nef protein was poorly incorporated into viral particles, and viral infectivity decreased dramatically. Thus, Nef also transports newly synthesized cholesterol to the site of viral budding. As such, it provides essential building blocks for the formation of viruses that replicate optimally in the host.
引用
收藏
页码:8460 / 8465
页数:6
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