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Dynamics of the base of ribosomal A-site finger revealed by molecular dynamics simulations and Cryo-EM

机译:分子动力学模拟和Cryo-EM揭示了核糖体A位手指基部的动力学

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Helix 38 (H38) of the large ribosomal subunit, with a length of 110 ?, reaches the small subunit through intersubunit bridge B1a. Previous cryo-EM studies revealed that the tip of H38 moves by more than 10 ? from the non-ratcheted to the ratcheted state of the ribosome while mutational studies implicated a key role of flexible H38 in attenuation of translocation and in dynamical signaling between ribosomal functional centers. We investigate a region including the elbow-shaped kink-turn (Kt-38) in the Haloarcula marismortui archaeal ribosome, and equivalently positioned elbows in three eubacterial species, located at the H38 base. We performed explicit solvent molecular dynamics simulations on the H38 elbows in all four species. They are formed by at first sight unrelated sequences resulting in diverse base interactions but built with the same overall topology, as shown by X-ray crystallography. The elbows display similar fluctuations and intrinsic flexibilities in simulations indicating that the eubacterial H38 elbows are structural and dynamical analogs of archaeal Kt-38. We suggest that this structural element plays a pivotal role in the large motions of H38 and may act as fulcrum for the abovementioned tip motion. The directional flexibility inferred from simulations correlates well with the cryo-EM results.
机译:大核糖体亚基的螺旋38(H38)的长度为110?,通过亚基间桥B1a到达小亚基。先前的冷冻EM研究表明,H38的尖端移动了10?从核糖体的非棘齿状态到棘齿状态,而突变研究则暗示了柔性H38在减缓转运和核糖体功能中心之间的动态信号传导中的关键作用。我们调查了一个区域,其中包括Haloarcula marismortui古细菌核糖体中的肘形扭折弯(Kt-38),以及位于H38基地的三个真细菌物种中的等位肘。我们对所有四个物种的H38弯头进行了显式的溶剂分子动力学模拟。它们是由乍一看无关的序列形成的,这些序列导致各种碱基相互作用,但具有相同的整体拓扑结构,如X射线晶体学所示。肘部在模拟中显示出相似的波动和固有灵活性,表明真细菌H38肘部是古细菌Kt-38的结构和动力学类似物。我们建议该结构元素在H38的大运动中起关键作用,并且可以充当上述尖端运动的支点。从仿真中推断出的方向灵活性与cryo-EM结果紧密相关。

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