Literature DB >> 9572840

Identification of unfolding domains in large proteins by their unfolding rates.

Y Deng1, D L Smith.   

Abstract

Three unfolding domains in rabbit muscle aldolase destabilized in 3 M urea have been identified from their unfolding rate constants (0.10, 0.036, and 0.0064 min-1). The populations of folded and various, partially unfolded forms were determined by amide hydrogen exchange and mass spectrometry. Results of this study show that unfolding domains may include multiple, noncontiguous segments of the backbone and that different regions of helices may belong to different unfolding domains. In addition, these results show that the domain unfolding most rapidly is located distant from the subunit binding surfaces and has the greatest access to the denaturant. The bimodal intermolecular distributions of deuterium found in this study show that unfolding of these domains is cooperative. It is proposed that these unfolding domains are correlated with local energy minima in the free-energy folding surface of aldolase. In addition to the three unfolding domains, there are three short segments that do not unfold in 3 M urea. These segments, which are located in the subunit binding surface, identify the most stable regions of aldolase. This study also demonstrates that it is now possible to identify and characterize unfolding domains in relatively large (Mr 158 000) proteins.

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Year:  1998        PMID: 9572840     DOI: 10.1021/bi972711o

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


  16 in total

Review 1.  The hydrogen exchange core and protein folding.

Authors:  R Li; C Woodward
Journal:  Protein Sci       Date:  1999-08       Impact factor: 6.725

2.  Scope and utility of hydrogen exchange as a tool for mapping landscapes.

Authors:  Sheila S Jaswal; Andrew D Miranker
Journal:  Protein Sci       Date:  2007-11       Impact factor: 6.725

3.  Analyzing protein dynamics using hydrogen exchange mass spectrometry.

Authors:  Nikolai Hentze; Matthias P Mayer
Journal:  J Vis Exp       Date:  2013-11-29       Impact factor: 1.355

Review 4.  Hydrogen exchange mass spectrometry: are we out of the quicksand?

Authors:  Roxana E Iacob; John R Engen
Journal:  J Am Soc Mass Spectrom       Date:  2012-04-03       Impact factor: 3.109

5.  Comparison of continuous and pulsed labeling amide hydrogen exchange/mass spectrometry for studies of protein dynamics.

Authors:  Y Deng; Z Zhang; D L Smith
Journal:  J Am Soc Mass Spectrom       Date:  1999-08       Impact factor: 3.109

6.  Matrix-assisted laser desorption ionization hydrogen/deuterium exchange studies to probe peptide conformational changes.

Authors:  I D Figueroa; D H Russell
Journal:  J Am Soc Mass Spectrom       Date:  1999-08       Impact factor: 3.109

7.  Allosteric suppression of HIV-1 reverse transcriptase structural dynamics upon inhibitor binding.

Authors:  James M Seckler; Mary D Barkley; Patrick L Wintrode
Journal:  Biophys J       Date:  2011-01-05       Impact factor: 4.033

8.  The folding energy landscape of the dimerization domain of Escherichia coli Trp repressor: a joint experimental and theoretical investigation.

Authors:  B Robert Simler; Yaakov Levy; José N Onuchic; C Robert Matthews
Journal:  J Mol Biol       Date:  2006-08-02       Impact factor: 5.469

9.  Investigating solution-phase protein structure and dynamics by hydrogen exchange mass spectrometry.

Authors:  Christopher R Morgan; John R Engen
Journal:  Curr Protoc Protein Sci       Date:  2009-11

10.  The gramicidin dimer shows both EX1 and EX2 mechanisms of H/D exchange.

Authors:  Raghu K Chitta; Don L Rempel; Michael L Gross
Journal:  J Am Soc Mass Spectrom       Date:  2009-06-21       Impact factor: 3.109

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