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-1 移码途径模型:动力学

Model of the pathway of -1 frameshifting: Kinetics.

作者信息

Xie Ping

机构信息

Key Laboratory of Soft Matter Physics and Beijing National Laboratory for Condensed Matter Physics, Institute of Physics, Chinese Academy of Sciences, Beijing 100190, China.

出版信息

Biochem Biophys Rep. 2016 Feb 10;5:453-467. doi: 10.1016/j.bbrep.2016.02.008. eCollection 2016 Mar.

Abstract

Programmed -1 translational frameshifting is a process where the translating ribosome shifts the reading frame, which is directed by at least two stimulatory elements in the mRNA-a slippery sequence and a downstream secondary structure. Despite a lot of theoretical and experimental studies, the detailed pathway and mechanism of the -1 frameshifting remain unclear. Here, in order to understand the pathway and mechanism we consider two models to study the kinetics of the -1 frameshifting, providing quantitative explanations of the recent biochemical data of Caliskan et al. (Cell 2014, 157, 1619-1631). One model is modified from that proposed by Caliskan et al. and the other is modified from that proposed in the previous work to explain the single-molecule experimental data. It is shown that by adjusting values of some fundamental parameters both models can give quantitative explanations of the biochemical data of Caliskan et al. on the kinetics of EF-G binding and dissociation and on the kinetics of movement of tRNAs inside the ribosome. However, for the former model some adjusted parameter values deviate significantly from those determined from the available single-molecule experiments, while for the latter model all parameter values are consistent with the available biochemical and single-molecule experimental data. Thus, the latter model most likely reflects the pathway and mechanism of the -1 frameshifting.

摘要

程序性 -1 翻译移码是一种翻译核糖体改变阅读框的过程,该过程由 mRNA 中的至少两个刺激元件引导——一个滑序列和一个下游二级结构。尽管进行了大量的理论和实验研究,但 -1 移码的详细途径和机制仍不清楚。在此,为了理解该途径和机制,我们考虑两个模型来研究 -1 移码的动力学,对 Caliskan 等人(《细胞》,2014 年,第 157 卷,第 1619 - 1631 页)最近的生化数据提供定量解释。一个模型是对 Caliskan 等人提出的模型进行修改,另一个模型是对先前工作中提出的模型进行修改以解释单分子实验数据。结果表明,通过调整一些基本参数的值,两个模型都可以对 Caliskan 等人关于 EF - G 结合和解离动力学以及核糖体内部 tRNA 移动动力学的生化数据给出定量解释。然而,对于前一个模型,一些调整后的参数值与从现有单分子实验确定的值有显著偏差,而后一个模型的所有参数值都与现有的生化和单分子实验数据一致。因此,后一个模型最有可能反映 -1 移码的途径和机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e816/5600437/ce198cdc20e0/gr1.jpg

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