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调节 HIV-1 病毒 Vpr 蛋白的通道形成片段的活性。

Modulating the activity of the channel-forming segment of Vpr protein from HIV-1.

机构信息

Institute of Biophotonics, School of Biomedical Science and Engineering, National Yang Ming University, Taipei, 112, Taiwan.

出版信息

Eur Biophys J. 2010 Jun;39(7):1089-95. doi: 10.1007/s00249-009-0518-x. Epub 2009 Jul 24.

Abstract

Viral protein of regulation (Vpr) encoded by human immunodeficiency virus type 1 (HIV-1) is a short auxiliary protein that is 96 amino acids in length. During the viral life cycle, Vpr is released into the blood serum and is able to enter cellular membranes of noninfected cells. In this study a short peptide, Vpr(55-83), was shown to exhibit ion-channel-like activity when reconstituted into (1) planar lipid bilayers and (2) lipid bilayers held at the tip of a glass pipette. The two set-ups led to differences in the oligomerization state of the peptide, which was reflected in differences in the conductance levels. Experiments under applied hydrostatic pressure affect the dynamics of the protein within the membrane.

摘要

人类免疫缺陷病毒 1 型(HIV-1)编码的病毒蛋白调节因子(Vpr)是一种短辅助蛋白,长度为 96 个氨基酸。在病毒生命周期中,Vpr 被释放到血清中,并能够进入未感染细胞的细胞膜。在这项研究中,当短肽 Vpr(55-83)被重建到(1)平面脂质双层和(2)玻璃吸管尖端的脂质双层中时,显示出离子通道样活性。这两种设置导致肽的寡聚状态的差异,这反映在电导水平的差异上。施加静水压力的实验会影响膜内蛋白质的动力学。

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