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Kinetic model for the ATP-dependent translocation of Saccharomyces cerevisiae RSC along double-stranded DNA

机译:双链DNA的ATP依赖性酿酒酵母RSC的ATP依赖性易位动力学模型

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The chromatin remodeling complex RSC from Saccharomyces cerevisiae is a DNA translocase that moves with directionality along double-stranded DNA in a reaction that is coupled to ATP hydrolysis. To better understand how this basic molecular motor functions, a novel method of analysis has been developed to study the kinetics of RSC translocation along double-stranded DNA. The data provided are consistent with RSC translocation occurring through a series of repeating uniform steps with an overall processivity of P = 0.949 +/- 0.003; this processivity corresponds to an average translocation distance of 20 I base pairs (bp) before dissociation. Interestingly, a slow initiation process, following DNA binding, is required to make RSC competent for DNA translocation. These results are further discussed in the context of previously published studies of RSC and other DNA translocases.
机译:来自Saccharomyces CereVisiae的染色质重塑RSC是一种DNA易位酶,其在与ATP水解偶联的反应中沿双链DNA的方向性移动。 为了更好地了解这种基本分子运动功能,已经开发了一种新的分析方法,以研究RSC易位沿双链DNA的动力学。 提供的数据与通过一系列重复均匀步骤发生的RSC易位,整体处理率为P = 0.949 +/- 0.003; 该处理器对应于解离之前20 I基对(BP)的平均易位距离。 有趣的是,在DNA结合后,需要缓慢的启动过程,以使RSC能力进行DNA易位。 在先前公布的RSC和其他DNA易位性研究的上下文中进一步讨论了这些结果。

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