Literature DB >> 18468622

Determination of the physiological dimer interface of the PhoQ sensor domain.

Shalom D Goldberg1, Cinque S Soto, Carey D Waldburger, William F Degrado.   

Abstract

PhoQ is the transmembrane sensor kinase of the phoPQ two-component system, which detects and responds to divalent cations and antimicrobial peptides and can trigger bacterial virulence. Despite their ubiquity and importance in bacterial signaling, the structure and molecular mechanism of the sensor kinases is not fully understood. Frequently, signals are transmitted from a periplasmic domain in these proteins to the cytoplasmic kinase domains via an extended dimeric interface, and the PhoQ protein would appear to follow this paradigm. However, the isolated truncated periplasmic domain of PhoQ dimerizes poorly, so it has been difficult to distinguish the relevant interface in crystal structures of the PhoQ periplasmic domain. Thus, to determine the arrangement of the periplasmic domains of Escherichia coli PhoQ in the physiological homodimer, disulfide-scanning mutagenesis was used. Single cysteine substitutions were introduced along the N-terminal helix of the periplasmic region, and the degree of cross-linking in each protein variant was determined by Western blotting and immunodetection. The results were subjected to periodicity analysis to generate a profile that provides information concerning the C(beta) distances between corresponding residues at the interface. This profile, together with a rigid-body search procedure, side-chain placement, and energy minimization, was used to build a model of the dimer arrangement. The final model proved to be highly compatible with one of the PhoQ crystal structures, 3BQ8, indicating that 3BQ8 is representative of the physiological arrangement. The model of the periplasmic region is also compatible with a full-length PhoQ protein in which a four-helix bundle forms in the membrane. The membrane four-helix bundle has been proposed for other sensor kinases and is thought to have a role in the mechanism of signal transduction; our model supports the idea that signaling through a membrane four-helix bundle is a widespread mechanism in the transmembrane sensor kinases.

Entities:  

Mesh:

Substances:

Year:  2008        PMID: 18468622      PMCID: PMC2542651          DOI: 10.1016/j.jmb.2008.04.023

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  44 in total

Review 1.  Transmembrane signaling in bacterial chemoreceptors.

Authors:  J J Falke; G L Hazelbauer
Journal:  Trends Biochem Sci       Date:  2001-04       Impact factor: 13.807

2.  Extending the accuracy limits of prediction for side-chain conformations.

Authors:  Z Xiang; B Honig
Journal:  J Mol Biol       Date:  2001-08-10       Impact factor: 5.469

3.  The Xplor-NIH NMR molecular structure determination package.

Authors:  Charles D Schwieters; John J Kuszewski; Nico Tjandra; G Marius Clore
Journal:  J Magn Reson       Date:  2003-01       Impact factor: 2.229

4.  Diagnostic cross-linking of paired cysteine pairs demonstrates homologous structures for two chemoreceptor domains with low sequence identity.

Authors:  Wing-Cheung Lai; Megan L Peach; Terry P Lybrand; Gerald L Hazelbauer
Journal:  Protein Sci       Date:  2005-12-01       Impact factor: 6.725

5.  Modeling the transmembrane domain of bacterial chemoreceptors.

Authors:  Megan L Peach; Gerald L Hazelbauer; Terry P Lybrand
Journal:  Protein Sci       Date:  2002-04       Impact factor: 6.725

6.  Site-directed cross-linking. Establishing the dimeric structure of the aspartate receptor of bacterial chemotaxis.

Authors:  D L Milligan; D E Koshland
Journal:  J Biol Chem       Date:  1988-05-05       Impact factor: 5.157

7.  Recognition of antimicrobial peptides by a bacterial sensor kinase.

Authors:  Martin W Bader; Sarah Sanowar; Margaret E Daley; Anna R Schneider; Uhnsoo Cho; Wenqing Xu; Rachel E Klevit; Hervé Le Moual; Samuel I Miller
Journal:  Cell       Date:  2005-08-12       Impact factor: 41.582

8.  The tolC locus of Escherichia coli affects the expression of three major outer membrane proteins.

Authors:  R Morona; P Reeves
Journal:  J Bacteriol       Date:  1982-06       Impact factor: 3.490

9.  The structure of the periplasmic ligand-binding domain of the sensor kinase CitA reveals the first extracellular PAS domain.

Authors:  Stefan Reinelt; Eckhard Hofmann; Tanja Gerharz; Michael Bott; Dean R Madden
Journal:  J Biol Chem       Date:  2003-07-16       Impact factor: 5.157

10.  The PAS fold. A redefinition of the PAS domain based upon structural prediction.

Authors:  Marco H Hefti; Kees-Jan Françoijs; Sacco C de Vries; Ray Dixon; Jacques Vervoort
Journal:  Eur J Biochem       Date:  2004-03
View more
  11 in total

1.  FeuN, a novel modulator of two-component signalling identified in Sinorhizobium meliloti.

Authors:  Rebecca E Carlyon; Joanna L Ryther; Ryan D VanYperen; Joel S Griffitts
Journal:  Mol Microbiol       Date:  2010-05-04       Impact factor: 3.501

Review 2.  Design and engineering of artificial oxygen-activating metalloenzymes.

Authors:  Flavia Nastri; Marco Chino; Ornella Maglio; Ambika Bhagi-Damodaran; Yi Lu; Angela Lombardi
Journal:  Chem Soc Rev       Date:  2016-06-24       Impact factor: 54.564

3.  The integrity of the periplasmic domain of the VirA sensor kinase is critical for optimal coordination of the virulence signal response in Agrobacterium tumefaciens.

Authors:  Gauri R Nair; Xiaoqin Lai; Arlene A Wise; Benjamin Wonjae Rhee; Mark Jacobs; Andrew N Binns
Journal:  J Bacteriol       Date:  2011-01-07       Impact factor: 3.490

4.  Transmembrane polar interactions are required for signaling in the Escherichia coli sensor kinase PhoQ.

Authors:  Shalom D Goldberg; Graham D Clinthorne; Mark Goulian; William F DeGrado
Journal:  Proc Natl Acad Sci U S A       Date:  2010-04-19       Impact factor: 11.205

5.  Probing designability via a generalized model of helical bundle geometry.

Authors:  Gevorg Grigoryan; William F Degrado
Journal:  J Mol Biol       Date:  2010-10-07       Impact factor: 5.469

6.  Biological insights from structures of two-component proteins.

Authors:  Rong Gao; Ann M Stock
Journal:  Annu Rev Microbiol       Date:  2009       Impact factor: 15.500

7.  Cys-scanning disulfide crosslinking and bayesian modeling probe the transmembrane signaling mechanism of the histidine kinase, PhoQ.

Authors:  Kathleen S Molnar; Massimiliano Bonomi; Riccardo Pellarin; Graham D Clinthorne; Gabriel Gonzalez; Shalom D Goldberg; Mark Goulian; Andrej Sali; William F DeGrado
Journal:  Structure       Date:  2014-07-31       Impact factor: 5.006

8.  The histidine kinase CusS senses silver ions through direct binding by its sensor domain.

Authors:  Swapna A Gudipaty; Megan M McEvoy
Journal:  Biochim Biophys Acta       Date:  2014-06-16

9.  Feedback inhibition in the PhoQ/PhoP signaling system by a membrane peptide.

Authors:  Andrew M Lippa; Mark Goulian
Journal:  PLoS Genet       Date:  2009-12-24       Impact factor: 5.917

10.  Assembly of the transmembrane domain of E. coli PhoQ histidine kinase: implications for signal transduction from molecular simulations.

Authors:  Thomas Lemmin; Cinque S Soto; Graham Clinthorne; William F DeGrado; Matteo Dal Peraro
Journal:  PLoS Comput Biol       Date:  2013-01-24       Impact factor: 4.475

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.