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通过电子显微镜密度图和分子动力学模拟分析的反密码子转运RNA反向通过核糖体的自由能景观。

Free-energy landscape of reverse tRNA translocation through the ribosome analyzed by electron microscopy density maps and molecular dynamics simulations.

作者信息

Ishida Hisashi, Matsumoto Atsushi

机构信息

Quantum Beam Science Directorate and Center for Computational Science and e-Systems, Japan Atomic Energy Agency, Kyoto, Japan.

出版信息

PLoS One. 2014 Jul 7;9(7):e101951. doi: 10.1371/journal.pone.0101951. eCollection 2014.

Abstract

To understand the mechanism of reverse tRNA translocation in the ribosome, all-atom molecular dynamics simulations of the ribosome-tRNAs-mRNA-EFG complex were performed. The complex at the post-translocational state was directed towards the translocational and pre-translocational states by fitting the complex into cryo-EM density maps. Between a series of the fitting simulations, umbrella sampling simulations were performed to obtain the free-energy landscape. Multistep structural changes, such as a ratchet-like motion and rotation of the head of the small subunit were observed. The free-energy landscape showed that there were two main free-energy barriers: one between the post-translocational and intermediate states, and the other between the pre-translocational and intermediate states. The former corresponded to a clockwise rotation, which was coupled to the movement of P-tRNA over the P/E-gate made of G1338, A1339 and A790 in the small subunit. The latter corresponded to an anticlockwise rotation of the head, which was coupled to the location of the two tRNAs in the hybrid state. This indicates that the coupled motion of the head rotation and tRNA translocation plays an important role in opening and closing of the P/E-gate during the ratchet-like movement in the ribosome. Conformational change of EF-G was interpreted to be the result of the combination of the external motion by L12 around an axis passing near the sarcin-ricin loop, and internal hinge-bending motion. These motions contributed to the movement of domain IV of EF-G to maintain its interaction with A/P-tRNA.

摘要

为了解核糖体中反向tRNA易位的机制,我们对核糖体 - tRNAs - mRNA - EFG复合物进行了全原子分子动力学模拟。通过将复合物拟合到冷冻电镜密度图中,使处于转位后状态的复合物转变为转位状态和转位前状态。在一系列拟合模拟之间,进行了伞形抽样模拟以获得自由能景观。观察到了多步结构变化,例如小亚基头部的棘轮样运动和旋转。自由能景观表明存在两个主要的自由能屏障:一个在转位后状态和中间状态之间,另一个在转位前状态和中间状态之间。前者对应于顺时针旋转,这与P - tRNA在小亚基中由G1338、A1339和A790构成的P/E门上方的移动相关联。后者对应于头部的逆时针旋转,这与处于杂交状态的两个tRNA的定位相关联。这表明在核糖体的棘轮样运动过程中,头部旋转和tRNA易位的耦合运动在P/E门的打开和关闭中起重要作用。EF - G的构象变化被解释为L12围绕靠近肌动蛋白 - 蓖麻毒素环的轴进行的外部运动与内部铰链弯曲运动相结合的结果。这些运动有助于EF - G的结构域IV的移动,以维持其与A/P - tRNA的相互作用。

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