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
DOI10.1073/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;
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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.
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