دورية أكاديمية

Analyzing the interaction of RseA and RseB, the two negative regulators of the sigmaE envelope stress response, using a combined bioinformatic and experimental strategy.

التفاصيل البيبلوغرافية
العنوان: Analyzing the interaction of RseA and RseB, the two negative regulators of the sigmaE envelope stress response, using a combined bioinformatic and experimental strategy.
المؤلفون: Ahuja N; Department of Microbiology and Immunology, University of California, San Francisco, California 94158, USA., Korkin D, Chaba R, Cezairliyan BO, Sauer RT, Kim KK, Gross CA
المصدر: The Journal of biological chemistry [J Biol Chem] 2009 Feb 20; Vol. 284 (8), pp. 5403-13. Date of Electronic Publication: 2008 Dec 22.
نوع المنشور: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
اللغة: English
بيانات الدورية: Publisher: Elsevier Inc. on behalf of American Society for Biochemistry and Molecular Biology Country of Publication: United States NLM ID: 2985121R Publication Model: Print-Electronic Cited Medium: Print ISSN: 0021-9258 (Print) Linking ISSN: 00219258 NLM ISO Abbreviation: J Biol Chem Subsets: MEDLINE
أسماء مطبوعة: Publication: 2021- : [New York, NY] : Elsevier Inc. on behalf of American Society for Biochemistry and Molecular Biology
Original Publication: Baltimore, MD : American Society for Biochemistry and Molecular Biology
مواضيع طبية MeSH: Escherichia coli/*metabolism , Escherichia coli Proteins/*metabolism , Membrane Proteins/*metabolism , Sigma Factor/*metabolism , Transcription Factors/*metabolism, Amino Acid Substitution ; Computational Biology/methods ; Disulfides/metabolism ; Escherichia coli/genetics ; Escherichia coli Proteins/genetics ; Membrane Proteins/genetics ; Mutation, Missense ; Protein Binding/physiology ; Protein Structure, Tertiary/physiology ; Sigma Factor/genetics ; Transcription Factors/genetics
مستخلص: The Escherichia coli envelope stress response is controlled by the alternative sigma factor, sigma(E), and is induced when unfolded outer membrane proteins accumulate in the periplasm. The response is initiated by sequential cleavage of the membrane-spanning antisigma factor, RseA. RseB is an important negative regulator of envelope stress response that exerts its negative effects onsigma(E) activity through its binding to RseA. In this study, we analyze the interaction between RseA and RseB. We found that tight binding of RseB to RseA required intact RseB. Using programs that performed global and local sequence alignment of RseB and RseA, we found regions of high similarity and performed alanine substitution mutagenesis to test the hypothesis that these regions were functionally important. This protocol is based on the hypothesis that functionally dependent regions of two proteins co-evolve and therefore are likely to be sequentially conserved. This procedure allowed us to identify both an N-terminal and C-terminal region in RseB important for binding to RseA. We extensively analyzed the C-terminal region, which aligns with a region of RseA coincident with the major RseB binding determinant in RseA. Both allele-specific suppression analysis and cysteine-mediated disulfide bond formation indicated that this C-terminal region of similarity of RseA and RseB identifies a contact site between the two proteins. We suggest a similar protocol can be successfully applied to pairs of non-homologous but functionally linked proteins to find specific regions of the protein sequences that are important for establishing functional linkage.
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معلومات مُعتمدة: AI-16892 United States AI NIAID NIH HHS; GM-32678 United States GM NIGMS NIH HHS
المشرفين على المادة: 0 (Disulfides)
0 (Escherichia coli Proteins)
0 (Membrane Proteins)
0 (RseA protein, E coli)
0 (RseB protein, E coli)
0 (Sigma Factor)
0 (Transcription Factors)
0 (sporulation-specific sigma factors)
تواريخ الأحداث: Date Created: 20081224 Date Completed: 20090413 Latest Revision: 20211020
رمز التحديث: 20221213
مُعرف محوري في PubMed: PMC2643490
DOI: 10.1074/jbc.M806012200
PMID: 19103591
قاعدة البيانات: MEDLINE
الوصف
تدمد:0021-9258
DOI:10.1074/jbc.M806012200