Zimmermann Michael T, Jia Kejue, Jernigan Robert L
Jernigan Laboratory, Iowa State University, Ames, IA 50011, USA.
Department of Biochemistry, Biophysics, and Molecular Biology, Iowa State University, Ames, IA 50011, USA.
J Mol Biol. 2016 Feb 27;428(5 Pt A):802-810. doi: 10.1016/j.jmb.2015.12.003. Epub 2015 Dec 11.
The essential aspects of the ribosome's mechanism can be extracted from coarse-grained simulations, including the ratchet motion, the movement together of critical bases at the decoding center, and movements of the peptide tunnel lining that assist in the expulsion of the synthesized peptide. Because of its large size, coarse graining helps to simplify and to aid in the understanding of its mechanism. Results presented here utilize coarse-grained elastic network modeling to extract the dynamics, and both RNAs and proteins are coarse grained. We review our previous results, showing the well-known ratchet motions and the motions in the peptide tunnel and in the mRNA tunnel. The motions of the lining of the peptide tunnel appear to assist in the expulsion of the growing peptide chain, and clamps at the ends of the mRNA tunnel with three proteins ensure that the mRNA is held tightly during decoding and essential for the helicase activity at the entrance. The entry clamp may also assist in base recognition to ensure proper selection of the incoming tRNA. The overall precision of the ribosome machine-like motions is remarkable.
核糖体机制的基本方面可以从粗粒度模拟中提取出来,包括棘轮运动、解码中心关键碱基的协同运动以及肽通道内衬的运动,这些运动有助于排出合成的肽。由于核糖体尺寸较大,粗粒度有助于简化并辅助理解其机制。此处展示的结果利用粗粒度弹性网络模型来提取动力学信息,RNA和蛋白质均进行了粗粒度处理。我们回顾了之前的结果,展示了众所周知的棘轮运动以及肽通道和mRNA通道中的运动。肽通道内衬的运动似乎有助于排出不断增长的肽链,mRNA通道两端由三种蛋白质构成的夹子可确保在解码过程中mRNA被紧紧固定,这对于入口处解旋酶的活性至关重要。入口夹子也可能有助于碱基识别,以确保正确选择进入的tRNA。核糖体类似机器的运动的整体精度非常显著。