Department of Chemistry and Chemical Biology, Harvard University, Cambridge, Massachusetts, USA.
Nat Struct Mol Biol. 2010 Dec;17(12):1453-60. doi: 10.1038/nsmb.1937. Epub 2010 Nov 21.
Human immunodeficiency virus (HIV) initiates reverse transcription of its viral RNA (vRNA) genome from a cellular tRNA(3)(Lys) primer. This process is characterized by a slow initiation phase with specific pauses, followed by a fast elongation phase. We report a single-molecule study that monitors the dynamics of individual initiation complexes, comprised of vRNA, tRNA and HIV reverse transcriptase (RT). RT transitions between two opposite binding orientations on tRNA-vRNA complexes, and the prominent pausing events are related to RT binding in a flipped orientation opposite to the polymerization-competent configuration. A stem-loop structure within the vRNA is responsible for maintaining the enzyme predominantly in this flipped orientation. Disruption of the stem-loop structure triggers the initiation-to-elongation transition. These results highlight the important role of the structural dynamics of the initiation complex in directing transitions between early reverse transcription phases.
人类免疫缺陷病毒 (HIV) 从细胞转移 RNA(tRNA)(3)(Lys) 引物开始逆转录其病毒 RNA (vRNA) 基因组。这个过程的特点是具有特定停顿的缓慢起始阶段,随后是快速延伸阶段。我们报告了一项单分子研究,该研究监测了由 vRNA、tRNA 和 HIV 逆转录酶 (RT) 组成的单个起始复合物的动力学。RT 在 tRNA-vRNA 复合物上的两种相反结合方向之间转换,而突出的暂停事件与 RT 以与聚合能力构型相反的翻转构型结合有关。vRNA 内的茎环结构负责使酶主要保持在这种翻转取向。茎环结构的破坏触发了起始到延伸的转变。这些结果强调了起始复合物结构动力学在指导早期逆转录阶段之间转变中的重要作用。