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真核生物翻译起始过程中核糖体亚基结合的机制。

Mechanism of ribosomal subunit joining during eukaryotic translation initiation.

作者信息

Acker Michael G, Lorsch Jon R

机构信息

Department of Biophysics and Biophysical Chemistry, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.

出版信息

Biochem Soc Trans. 2008 Aug;36(Pt 4):653-7. doi: 10.1042/BST0360653.

Abstract

Decades of research have yielded significant insight into the mechanism by which a cell translates an mRNA into the encoded protein. However many of the molecular details of the process remain a mystery. Translation initiation is an important control point in gene expression, and misregulation can lead to diseases such as cancer. A better understanding of the mechanism of translation initiation is imperative for the development of novel therapeutic agents. Recently, a combination of genetic, biochemical and biophysical studies has begun to shed light on how, at a molecular level, the translational machinery initiates protein synthesis. In the present review, we briefly compare and contrast the initiation pathways utilized by bacteria, archaea and eukaryotes, and then focus on translation initiation in eukaryotes and recent advances in our understanding of the subunit joining step of the process.

摘要

数十年来的研究已对细胞将信使核糖核酸(mRNA)翻译成编码蛋白质的机制有了重要见解。然而,该过程的许多分子细节仍是个谜。翻译起始是基因表达中的一个重要控制点,调控异常会导致诸如癌症等疾病。更好地理解翻译起始机制对于新型治疗药物的开发至关重要。最近,遗传学、生物化学和生物物理学研究的结合已开始揭示翻译机制在分子水平上是如何启动蛋白质合成的。在本综述中,我们简要比较和对比了细菌、古细菌和真核生物所利用的起始途径,然后重点关注真核生物中的翻译起始以及我们对该过程亚基结合步骤理解的最新进展。

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