Literature DB >> 11863438

Salt bridges destabilize a leucine zipper designed for maximized ion pairing between helices.

Paul Phelan1, Alemayehu A Gorfe, Ilian Jelesarov, Daniel N Marti, James Warwicker, Hans Rudolf Bosshard.   

Abstract

Interhelical salt bridges are common in leucine zippers and are thought to stabilize the coiled coil conformation. Here we present a detailed thermodynamic investigation of the designed, disulfide-linked leucine zipper AB(SS) whose high-resolution NMR structure shows six interhelical ion pairs between heptad positions g of one helix and e' of the other helix but no ion pairing within single helices. The average pK(a) value of the Glu side chain carboxyl groups of AB(SS) is slightly higher than the pK(a) of a freely accessible Glu in an unfolded peptide [Marti, D. N., Jelesarov, I., and Bosshard, H. R. (2000) Biochemistry 39, 12804-12818]. This indicates that the salt bridges are destabilizing, a prediction we now have confirmed by determining the pH +/- stability profile of AB(SS). Circular dichroism-monitored unfolding by urea and by heating and differential scanning calorimetry show that the coiled coil conformation is approximately 5 kJ/mol more stable when salt bridges are broken by protonation of the carboxyl side chains. Using guanidinium chloride as the denaturant, the increase in the free energy of unfolding on protonation of the carboxyl side chains is larger, approximately 17 kJ/mol. The discrepancy between urea and guanidinium chloride unfolding can be ascribed to the ionic nature of guanidinium chloride, which screens charge-charge interactions. This work demonstrates the difficulty of predicting the energetic contribution of salt bridges from structural data alone even in a case where the ion pairs are seen in high-resolution NMR structures. The reason is that the contribution to stability results from a fine balance between energetically favorable Coulombic attractions and unfavorable desolvation of charges and conformational constraints of the residues involved in ion pairing. The apparent discrepancy between the results presented here and mutational studies indicating stabilization by salt bridges is discussed and resolved. An explanation is proposed for why interhelical salt bridges are frequently found in natural coiled coils despite evidence that they do not directly contribute to stability.

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Year:  2002        PMID: 11863438     DOI: 10.1021/bi011920c

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  9 in total

1.  Unique stabilizing interactions identified in the two-stranded alpha-helical coiled-coil: crystal structure of a cortexillin I/GCN4 hybrid coiled-coil peptide.

Authors:  Darin L Lee; Sergei Ivaninskii; Peter Burkhard; Robert S Hodges
Journal:  Protein Sci       Date:  2003-07       Impact factor: 6.725

2.  The effects of pK(a) tuning on the thermodynamics and kinetics of folding: design of a solvent-shielded carboxylate pair at the a-position of a coiled-coil.

Authors:  Wai Leung Lau; William F Degrado; Heinrich Roder
Journal:  Biophys J       Date:  2010-10-06       Impact factor: 4.033

3.  A localized specific interaction alters the unfolding pathways of structural homologues.

Authors:  Guoqiang Xu; Mahesh Narayan; Igor Kurinov; Daniel R Ripoll; Ervin Welker; Mey Khalili; Steven E Ealick; Harold A Scheraga
Journal:  J Am Chem Soc       Date:  2006-02-01       Impact factor: 15.419

4.  Influence of Glu/Arg, Asp/Arg, and Glu/Lys Salt Bridges on α-Helical Stability and Folding Kinetics.

Authors:  Heleen Meuzelaar; Jocelyne Vreede; Sander Woutersen
Journal:  Biophys J       Date:  2016-06-07       Impact factor: 4.033

5.  Critical interactions in the stability control region of tropomyosin.

Authors:  J Paul Kirwan; Robert S Hodges
Journal:  J Struct Biol       Date:  2010-02-06       Impact factor: 2.867

6.  Structural basis for the enhanced thermal stability of alcohol dehydrogenase mutants from the mesophilic bacterium Clostridium beijerinckii: contribution of salt bridging.

Authors:  Oren Bogin; Inna Levin; Yael Hacham; Shoshana Tel-Or; Moshe Peretz; Felix Frolow; Yigal Burstein
Journal:  Protein Sci       Date:  2002-11       Impact factor: 6.725

7.  Computational design of a collagen A:B:C-type heterotrimer.

Authors:  Fei Xu; Sohail Zahid; Teresita Silva; Vikas Nanda
Journal:  J Am Chem Soc       Date:  2011-09-14       Impact factor: 15.419

8.  Solvent-Exposed Salt Bridges Influence the Kinetics of α-Helix Folding and Unfolding.

Authors:  Heleen Meuzelaar; Martijn Tros; Adriana Huerta-Viga; Chris N van Dijk; Jocelyne Vreede; Sander Woutersen
Journal:  J Phys Chem Lett       Date:  2014-02-14       Impact factor: 6.475

9.  A new family of intrinsically disordered proteins: structural characterization of the major phasin PhaF from Pseudomonas putida KT2440.

Authors:  Beatriz Maestro; Beatriz Galán; Carlos Alfonso; Germán Rivas; Maria A Prieto; Jesús M Sanz
Journal:  PLoS One       Date:  2013-02-15       Impact factor: 3.240

  9 in total

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