Abrahamyan Levon G, Mkrtchyan Samvel R, Binley James, Lu Min, Melikyan Grigory B, Cohen Fredric S
Department of Molecular Biophysics and Physiology, Rush University Medical Center, Chicago, Illinois 60612, USA.
J Virol. 2005 Jan;79(1):106-15. doi: 10.1128/JVI.79.1.106-115.2005.
Effects of the cytoplasmic tail (CT) of human immunodeficiency virus type 1 Env on the process of membrane fusion were investigated. Full-length Env (wild type [WT]) and Env with its CT truncated (DeltaCT) were expressed on cell surfaces, these cells were fused to target cells, and the inhibition of fusion by peptides that prevent Env from folding into a six-helix bundle conformation was measured. For both X4-tropic and R5-tropic Env proteins, DeltaCT induced faster fusion kinetics than did the WT, and peptides were less effective at inhibiting DeltaCT-induced fusion. We tested the hypothesis that the inhibitory peptides were less effective at inhibiting DeltaCT-induced fusion because DeltaCT folds more quickly into a six-helix bundle. Early and late intermediates of WT- and DeltaCT-induced fusion were captured, and the ability of peptides to block fusion when added at the intermediate stages was quantified. When added at the early intermediate, the peptides were still less effective at inhibiting DeltaCT-induced fusion but they were equally effective at preventing WT- and DeltaCT-induced fusion when added at the late intermediate. We conclude that for both X4-tropic and R5-tropic Env proteins, the CT facilitates conformational changes that allow the trimeric coiled coil of prebundles to become optimally exposed. But once Env does favorably expose its coiled coil to inhibitory peptides, the CT hinders subsequent folding into a six-helix bundle. Because of this facilitation of maximal exposure and hindrance of bundle formation, the coiled coil is optimally exposed for a longer time for WT than for DeltaCT. This accounts for the greater peptide inhibition of WT-induced fusion.
研究了1型人类免疫缺陷病毒包膜蛋白(Env)的胞质尾(CT)对膜融合过程的影响。全长Env(野生型[WT])及其CT截短的Env(DeltaCT)在细胞表面表达,将这些细胞与靶细胞融合,并测量了可阻止Env折叠成六螺旋束构象的肽对融合的抑制作用。对于X4嗜性和R5嗜性Env蛋白,DeltaCT诱导的融合动力学比WT更快,并且肽对DeltaCT诱导的融合的抑制作用较小。我们检验了这样一个假设,即抑制性肽对DeltaCT诱导的融合抑制作用较小是因为DeltaCT更快地折叠成六螺旋束。捕获了WT和DeltaCT诱导融合的早期和晚期中间体,并对在中间体阶段添加肽时阻断融合的能力进行了定量。在早期中间体阶段添加时,肽对DeltaCT诱导的融合的抑制作用仍然较小,但在晚期中间体阶段添加时,它们对阻止WT和DeltaCT诱导的融合同样有效。我们得出结论,对于X4嗜性和R5嗜性Env蛋白,CT促进构象变化,使预束三聚体卷曲螺旋得以最佳暴露。但是一旦Env确实将其卷曲螺旋有利地暴露于抑制性肽,CT就会阻碍其随后折叠成六螺旋束。由于这种对最大暴露的促进和对束形成的阻碍,WT的卷曲螺旋比DeltaCT的卷曲螺旋在更长的时间内处于最佳暴露状态。这就解释了肽对WT诱导融合的更大抑制作用。