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解码谜局:人类线粒体中的翻译终止。

Decoding the Enigma: Translation Termination in Human Mitochondria.

机构信息

Department of Medical Biochemistry and Biophysics, Division of Molecular Metabolism, Karolinska Institutet, Solnavägen 9, Solna 171 65, Sweden.

出版信息

Hum Mol Genet. 2024 May 22;33(R1):R42-R46. doi: 10.1093/hmg/ddae032.

Abstract

Mitochondrial translation is a complex process responsible for the synthesis of essential proteins involved in oxidative phosphorylation, a fundamental pathway for cellular energy production. Central to this process is the termination phase, where dedicated factors play a pivotal role in ensuring accurate and timely protein production. This review provides a comprehensive overview of the current understanding of translation termination in human mitochondria, emphasizing structural features and molecular functions of two mitochondrial termination factors mtRF1 and mtRF1a.

摘要

线粒体翻译是一个复杂的过程,负责合成参与氧化磷酸化的必需蛋白质,氧化磷酸化是细胞能量产生的基本途径。这个过程的核心是终止阶段,专门的因子在确保蛋白质准确和及时的产生中起着关键作用。这篇综述提供了对人线粒体翻译终止的当前理解的全面概述,强调了两个线粒体终止因子 mtRF1 和 mtRF1a 的结构特征和分子功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57c8/11112381/43a573cc45d9/ddae032f1.jpg

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