Department of Medical Research, Mackay Memorial Hospital, Tamsui, Taiwan.
Biophys J. 2010 Sep 22;99(6):1718-25. doi: 10.1016/j.bpj.2010.07.027.
Vpu, a component unique to HIV-1, greatly enhances the efficiency of viral particle release by unclear mechanisms. This Vpu function is intrinsically linked to its channel-like structure, which enables it to interfere with homologous transmembrane structures in infected cells. Because Vpu interacts destructively with host background K(+) channels that set the cell resting potential, we hypothesized that Vpu might trigger viral release by destabilizing the electric field across a budding membrane. Here, we found that the efficiency of Vpu-mediated viral release is inversely correlated with membrane potential polarization. By inhibiting the background K(+) currents, Vpu dissipates the voltage constraint on viral particle discharge. As a proof of concept, we show that HIV-1 release can be accelerated by externally imposed depolarization alone. Our findings identify the trigger of Vpu-mediated release as a manifestation of the general principle of depolarization-stimulated exocytosis.
Vpu,一种 HIV-1 特有的成分,通过不明机制极大地提高了病毒粒子释放的效率。这种 Vpu 功能与其类似通道的结构密切相关,使其能够干扰受感染细胞中的同源跨膜结构。由于 Vpu 与宿主背景 K(+) 通道发生破坏性相互作用,后者设定了细胞静息电位,因此我们假设 Vpu 可能通过破坏萌芽膜的电场来触发病毒释放。在这里,我们发现 Vpu 介导的病毒释放效率与膜电位极化呈负相关。通过抑制背景 K(+) 电流,Vpu 消除了病毒粒子排出的电压限制。作为概念验证,我们表明仅通过外部施加去极化就可以加速 HIV-1 的释放。我们的发现将 Vpu 介导的释放的触发确定为去极化刺激胞吐作用的一般原理的表现。