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啤酒酵母Ubr1野生型和缺失型菌株的比较蛋白组学分析

彭健 陈杰 丁成明 夏赞贤 张耀婷 李慧 肖小龙 韦超盈 周宇筝 卢爱 张礼铭 周梅

中国现代医学杂志2017,Vol.27Issue(21):18-24,7.
中国现代医学杂志2017,Vol.27Issue(21):18-24,7.DOI:10.3969/j.issn.1005-8982.2017.21.004

啤酒酵母Ubr1野生型和缺失型菌株的比较蛋白组学分析

Comparative proteomic analysis of Ubr1 wild type and deletion type of Saccharomyces cerevisiae

彭健 1陈杰 1丁成明 1夏赞贤 2张耀婷 1李慧 2肖小龙 2韦超盈 2周宇筝 2卢爱 2张礼铭 2周梅2

作者信息

  • 1. 中南大学湘雅医院,湖南长沙410008
  • 2. 中南大学生命科学学院,湖南长沙410013
  • 折叠

摘要

Abstract

Objective To justify the rationality of proteomic screening on a large scale and identify potential substrates of Ubr1 with the approach.Methods In this work,comparative proteomic analysis between RJD347 (Ubr1 wild type) and AVY26 (Ubr1 deletion type) has been performed to screen the possible substrate proteins of Ubrl.Moreover,the correlation between the differentially expressed proteins and Ubr1 was further verified by protein work.Results In total,249 proteins which were differentially expressed were identified,of which 145 proteins were up-regulated in AVY26.Furthermore,the protein work confirmed 5 proteins including MLC2,SCD6,ARG1,HOG1 and RTF1 that were closely related to Ubr1.Conclusions A massive database of 249 proteins that are differentially expressed between RJD347 and AVY26 is established.Five potential substrates of Ubr1 ubiquitination proteins is identified,which provides the experimental basis for further understanding of biological processes of Ubr1.

关键词

啤酒酵母/泛素连接酶E3成分N-识别蛋白1/泛素化/蛋白质组学

Key words

Saccharomyces cerevisiae/ubiquitin protein ligase E3 component N-recognin 1/ubiquitination/proteomics

分类

生物科学

引用本文复制引用

彭健,陈杰,丁成明,夏赞贤,张耀婷,李慧,肖小龙,韦超盈,周宇筝,卢爱,张礼铭,周梅..啤酒酵母Ubr1野生型和缺失型菌株的比较蛋白组学分析[J].中国现代医学杂志,2017,27(21):18-24,7.

基金项目

国家自然科学基金联合项目(No:U1603126) (No:U1603126)

湖南省自然科学基金(No:2017JJ2334) (No:2017JJ2334)

中国现代医学杂志

OACSTPCD

1005-8982

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