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通过定制的串联质谱(MS/MS)谱数据库搜索鉴定线粒体无终止密码子蛋白质上NEMF介导的C末端延伸的方案。

Protocol for identification of NEMF-mediated C-terminal extensions on mitochondrial nonstop proteins via customized MS/MS spectra database searching.

作者信息

Chen Leijie, Mo Jinyou, Tan Yuyong, Lv Liang, Liu Jia

机构信息

Department of Gastroenterology, The Second Xiangya Hospital of Central South University, Changsha, Hunan 410011, China; Center for Medical Research, The Second Xiangya Hospital of Central South University, Changsha, Hunan 410011, China; Clinical Research Center for Digestive Diseases in Hunan Province, Changsha, Hunan 410011, China.

Center for Medical Research, The Second Xiangya Hospital of Central South University, Changsha, Hunan 410011, China.

出版信息

STAR Protoc. 2024 Dec 20;5(4):103366. doi: 10.1016/j.xpro.2024.103366. Epub 2024 Oct 11.

Abstract

The ribosome-associated protein quality control (RQC) core factor nuclear export mediator factor (NEMF) appends C-terminal extended sequences (CESs) to ribosome-stalled nascent chains (NCs). Specific CESs compositions could be directly recognized by enzymes and facilitate NC degradation. Yet, NEMF-mediated CESs remains largely unidentified. Here, we present a protocol for identifying and characterizing NEMF-mediated C-terminal modifications on mitochondrial NCs (mitoNCs) via tandem mass spectrometry (MS/MS) analysis. We describe strategies aimed at constructing a customized MS/MS spectra database for unknown CESs and detail the steps for CES-modified sample preparation. For complete details on the use and execution of this protocol, please refer to Lv et al..

摘要

核糖体相关蛋白质量控制(RQC)核心因子核输出介质因子(NEMF)会在核糖体停滞的新生链(NCs)上附加C端延伸序列(CESs)。特定的CESs组成可被酶直接识别并促进NCs的降解。然而,NEMF介导的CESs在很大程度上仍未明确。在此,我们提出了一种通过串联质谱(MS/MS)分析来鉴定和表征线粒体NCs(mitoNCs)上NEMF介导的C端修饰的方案。我们描述了旨在为未知CESs构建定制MS/MS谱数据库的策略,并详细说明了CES修饰样品制备的步骤。有关本方案使用和执行的完整详细信息,请参阅Lv等人的文章。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef89/11736100/2fed02cd057f/fx1.jpg

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