Literature DB >> 18501927

Hydrogen-exchange mass spectrometry reveals activation-induced changes in the conformational mobility of p38alpha MAP kinase.

Kevin M Sours1, Stan C Kwok, Thami Rachidi, Thomas Lee, Adam Ring, Andrew N Hoofnagle, Katheryn A Resing, Natalie G Ahn.   

Abstract

Hydrogen-deuterium exchange measurements represent a powerful approach to investigating changes in conformation and conformational mobility in proteins. Here, we examine p38alpha MAP kinase (MAPK) by hydrogen-exchange (HX) mass spectrometry to determine whether changes in conformational mobility may be induced by kinase phosphorylation and activation. Factors influencing sequence coverage in the HX mass spectrometry experiment, which show that varying sampling depths, instruments, and peptide search strategies yield the highest coverage of exchangeable amides, are examined. Patterns of regional deuteration in p38alpha are consistent with tertiary structure and similar to deuteration patterns previously determined for extracellular-signal-regulated kinase (ERK) 2, indicating that MAPKs are conserved with respect to the extent of local amide HX. Activation of p38alpha alters HX in five regions, which are interpreted by comparing X-ray structures of unphosphorylated p38alpha and X-ray structures of phosphorylated p38gamma. Conformational differences account for altered HX within the activation lip, the P+1 site, and the active site. In contrast, HX alterations are ascribed to activation-induced effects on conformational mobility, within substrate-docking sites (alphaF-alphaG, beta7-beta8), the C-terminal core (alphaE), and the N-terminal core region (beta4-beta5, alphaL16, alphaC). Activation also decreases HX in a 3-10 helix at the C-terminal extension of p38alpha. Although this helix in ERK2 forms a dimerization interface that becomes protected from HX upon activation, analytical ultracentrifugation shows that this does not occur in p38alpha because both unphosphorylated and diphosphorylated forms are monomeric. Finally, HX patterns in monophosphorylated p38alpha are similar to those in unphosphorylated kinase, indicating that the major activation lip remodeling events occur only after diphosphorylation. Importantly, patterns of activation-induced HX show differences between p38alpha and ERK2 despite their similarities in overall deuteration, suggesting that although MAPKs are closely related with respect to primary sequence and tertiary structure, they have distinct mechanisms for dynamic control of enzyme function.

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Year:  2008        PMID: 18501927      PMCID: PMC2782421          DOI: 10.1016/j.jmb.2008.04.044

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


  44 in total

1.  Phosphorylation-dependent changes in structure and dynamics in ERK2 detected by SDSL and EPR.

Authors:  Andrew N Hoofnagle; James W Stoner; Thomas Lee; Sandra S Eaton; Natalie G Ahn
Journal:  Biophys J       Date:  2004-01       Impact factor: 4.033

2.  Prediction of low-energy collision-induced dissociation spectra of peptides with three or more charges.

Authors:  Zhongqi Zhang
Journal:  Anal Chem       Date:  2005-10-01       Impact factor: 6.986

3.  Activation mechanism of the MAP kinase ERK2 by dual phosphorylation.

Authors:  B J Canagarajah; A Khokhlatchev; M H Cobb; E J Goldsmith
Journal:  Cell       Date:  1997-09-05       Impact factor: 41.582

Review 4.  Inhibition of p38 MAP kinase as a therapeutic strategy.

Authors:  J C Lee; S Kumar; D E Griswold; D C Underwood; B J Votta; J L Adams
Journal:  Immunopharmacology       Date:  2000-05

5.  Structures of p38alpha active mutants reveal conformational changes in L16 loop that induce autophosphorylation and activation.

Authors:  Ron Diskin; Mario Lebendiker; David Engelberg; Oded Livnah
Journal:  J Mol Biol       Date:  2006-08-22       Impact factor: 5.469

6.  Activation of the MAP kinase homologue RK requires the phosphorylation of Thr-180 and Tyr-182 and both residues are phosphorylated in chemically stressed KB cells.

Authors:  Y N Doza; A Cuenda; G M Thomas; P Cohen; A R Nebreda
Journal:  FEBS Lett       Date:  1995-05-08       Impact factor: 4.124

7.  Dynamics of cAPK type IIbeta activation revealed by enhanced amide H/2H exchange mass spectrometry (DXMS).

Authors:  Yoshimoto Hamuro; Kerri M Zawadzki; Jack S Kim; David D Stranz; Susan S Taylor; Virgil L Woods
Journal:  J Mol Biol       Date:  2003-04-11       Impact factor: 5.469

8.  Ordered phosphorylation of p42mapk by MAP kinase kinase.

Authors:  T A Haystead; P Dent; J Wu; C M Haystead; T W Sturgill
Journal:  FEBS Lett       Date:  1992-07-13       Impact factor: 4.124

9.  The structure of mitogen-activated protein kinase p38 at 2.1-A resolution.

Authors:  Z Wang; P C Harkins; R J Ulevitch; J Han; M H Cobb; E J Goldsmith
Journal:  Proc Natl Acad Sci U S A       Date:  1997-03-18       Impact factor: 11.205

10.  Pro-inflammatory cytokines and environmental stress cause p38 mitogen-activated protein kinase activation by dual phosphorylation on tyrosine and threonine.

Authors:  J Raingeaud; S Gupta; J S Rogers; M Dickens; J Han; R J Ulevitch; R J Davis
Journal:  J Biol Chem       Date:  1995-03-31       Impact factor: 5.157

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  21 in total

1.  Carboxyl-group footprinting maps the dimerization interface and phosphorylation-induced conformational changes of a membrane-associated tyrosine kinase.

Authors:  Hao Zhang; Wei Shen; Don Rempel; John Monsey; Ilan Vidavsky; Michael L Gross; Ron Bose
Journal:  Mol Cell Proteomics       Date:  2011-03-21       Impact factor: 5.911

2.  Phosphorylation in the catalytic cleft stabilizes and attracts domains of a phosphohexomutase.

Authors:  Jia Xu; Yingying Lee; Lesa J Beamer; Steven R Van Doren
Journal:  Biophys J       Date:  2015-01-20       Impact factor: 4.033

3.  Promotion of enzyme flexibility by dephosphorylation and coupling to the catalytic mechanism of a phosphohexomutase.

Authors:  Yingying Lee; Maria T Villar; Antonio Artigues; Lesa J Beamer
Journal:  J Biol Chem       Date:  2014-01-08       Impact factor: 5.157

4.  Analysis of MAP kinases by hydrogen exchange mass spectrometry.

Authors:  Kevin M Sours; Natalie G Ahn
Journal:  Methods Mol Biol       Date:  2010

Review 5.  Hydrogen tunneling links protein dynamics to enzyme catalysis.

Authors:  Judith P Klinman; Amnon Kohen
Journal:  Annu Rev Biochem       Date:  2013       Impact factor: 23.643

6.  Structural characterization of the catalytic γ and regulatory β subunits of phosphorylase kinase in the context of the hexadecameric enzyme complex.

Authors:  Mary Ashley Rimmer; Owen W Nadeau; Antonio Artigues; Gerald M Carlson
Journal:  Protein Sci       Date:  2017-11-21       Impact factor: 6.725

7.  p38β Mitogen-Activated Protein Kinase Modulates Its Own Basal Activity by Autophosphorylation of the Activating Residue Thr180 and the Inhibitory Residues Thr241 and Ser261.

Authors:  Jonah Beenstock; Dganit Melamed; Navit Mooshayef; Dafna Mordechay; Benjamin P Garfinkel; Natalie G Ahn; Arie Admon; David Engelberg
Journal:  Mol Cell Biol       Date:  2016-05-02       Impact factor: 4.272

Review 8.  Importance of protein dynamics during enzymatic C-H bond cleavage catalysis.

Authors:  Judith P Klinman
Journal:  Biochemistry       Date:  2013-02-12       Impact factor: 3.162

9.  T cell receptor-mediated activation of p38{alpha} by mono-phosphorylation of the activation loop results in altered substrate specificity.

Authors:  Paul R Mittelstadt; Hiroshi Yamaguchi; Ettore Appella; Jonathan D Ashwell
Journal:  J Biol Chem       Date:  2009-03-25       Impact factor: 5.157

10.  Global consequences of activation loop phosphorylation on protein kinase A.

Authors:  Jon M Steichen; Ganesh H Iyer; Sheng Li; S Adrian Saldanha; Michael S Deal; Virgil L Woods; Susan S Taylor
Journal:  J Biol Chem       Date:  2009-12-04       Impact factor: 5.157

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