Molecular mechanism of quinone signaling mediated through S-quinonization of a YodB family repressor QsrR | |
Ji, Quanjiang1; Zhang, Liang1; Jones, Marcus B.4; Sun, Fei1; Deng, Xin1; Liang, Haihua1; Cho, Hoonsik2; Brugarolas, Pedro1; Gao, Yihe N.1; Peterson, Scott N.4 | |
刊名 | PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA |
2013-03-26 | |
卷号 | 110期号:13页码:5010-5015 |
关键词 | thiol alkylation macrophage |
ISSN号 | 0027-8424 |
DOI | 10.1073/pnas.1219446110 |
文献子类 | Article |
英文摘要 | Quinone molecules are intracellular electron-transport carriers, as well as critical intra-and extracellular signals. However, transcriptional regulation of quinone signaling and its molecular basis are poorly understood. Here, we identify a thiol-stress-sensing regulator YodB family transcriptional regulator as a central component of quinone stress response of Staphylococcus aureus, which we have termed the quinone-sensing and response repressor (QsrR). We also identify and confirm an unprecedented quinone-sensing mechanism based on the S-quinonization of the essential residue Cys-5. Structural characterizations of the QsrR-DNA and QsrR-menadione complexes further reveal that the covalent association of menadione directly leads to the release of QsrR from operator DNA following a 10 degrees rigid-body rotation as well as a 9-angstrom elongation between the dimeric subunits. The molecular level characterization of this quinone-sensing transcriptional regulator provides critical insights into quinone-mediated gene regulation in human pathogens. |
资助项目 | National Institutes of Health (NIH) National Institute of Allergy and Infectious Diseases[AI074658] ; NIH[P50GM081892] |
WOS关键词 | STAPHYLOCOCCUS-AUREUS ; BACILLUS-SUBTILIS ; REDOX SWITCH ; NAD(P)H-QUINONE REDUCTASE ; 2-ELECTRON REDUCTION ; ENTEROBACTER-CLOACAE ; 2-COMPONENT SYSTEM ; SENSING REGULATOR ; STRUCTURAL BASIS ; OXIDATION |
WOS研究方向 | Science & Technology - Other Topics |
语种 | 英语 |
出版者 | NATL ACAD SCIENCES |
WOS记录号 | WOS:000318031900040 |
内容类型 | 期刊论文 |
源URL | [http://119.78.100.183/handle/2S10ELR8/277689] |
专题 | 药理学第三研究室 中科院受体结构与功能重点实验室 新药研究国家重点实验室 |
通讯作者 | He, Chuan |
作者单位 | 1.Univ Chicago, Dept Chem, Chicago, IL 60637 USA; 2.Indiana Univ Sch Med Northwest, Dept Microbiol & Immunol, Gary, IN 46408 USA; 3.Chinese Acad Sci, Shanghai Inst Mat Med, Drug Discovery & Design Ctr, State Key Lab Drug Res, Shanghai 201203, Peoples R China 4.Pathogen Funct Genom Resource Ctr, Infect Dis Grp, J Craig Venter Inst, Rockville, MD 20850 USA; |
推荐引用方式 GB/T 7714 | Ji, Quanjiang,Zhang, Liang,Jones, Marcus B.,et al. Molecular mechanism of quinone signaling mediated through S-quinonization of a YodB family repressor QsrR[J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA,2013,110(13):5010-5015. |
APA | Ji, Quanjiang.,Zhang, Liang.,Jones, Marcus B..,Sun, Fei.,Deng, Xin.,...&He, Chuan.(2013).Molecular mechanism of quinone signaling mediated through S-quinonization of a YodB family repressor QsrR.PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA,110(13),5010-5015. |
MLA | Ji, Quanjiang,et al."Molecular mechanism of quinone signaling mediated through S-quinonization of a YodB family repressor QsrR".PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 110.13(2013):5010-5015. |
个性服务 |
查看访问统计 |
相关权益政策 |
暂无数据 |
收藏/分享 |
除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。
修改评论