Literature DB >> 24214077

The complexation of protonated peptides with saccharides in the gas phase decreases the rates of hydrogen/deuterium exchange reactions.

M Kirk Green1, S G Penn, C B Lebrilla.   

Abstract

Gas-phase noncovalently bound complexes are probed by hydrogen/deuterium exchange. The complexes, composed of a protonated amino acid and a monosaccharide, are investigated to observe the effects of complexation on the rates of exchange. Rate constants are determined and compared for complexed and uncomplexed amino acids. The overall rate constant, which corresponds to exchange of a specific number of hydrogens, is deconvoluted to yield site-specific rate constants. Complexation of amino acids with saccharides significantly decreases the rate constants of the exchange. Results of molecular orbital calculations are provided to explain the decrease in the rates.

Entities:  

Year:  1995        PMID: 24214077     DOI: 10.1016/1044-0305(95)00632-X

Source DB:  PubMed          Journal:  J Am Soc Mass Spectrom        ISSN: 1044-0305            Impact factor:   3.109


  2 in total

1.  Gas-phase hydrogen/deuterium exchange as a molecular probe for the interaction of methanol and protonated peptides.

Authors:  E Gard; M K Green; J Bregar; C B Lebrilla
Journal:  J Am Soc Mass Spectrom       Date:  1994-07       Impact factor: 3.109

2.  Coexisting stable conformations of gaseous protein ions.

Authors:  D Suckau; Y Shi; S C Beu; M W Senko; J P Quinn; F M Wampler; F W McLafferty
Journal:  Proc Natl Acad Sci U S A       Date:  1993-02-01       Impact factor: 11.205

  2 in total
  4 in total

1.  Gas-phase H/D exchange reactions of polyamine complexes: (M + H)+, (M + alkali metal+), and (M + 2H)2+

Authors: 
Journal:  J Am Soc Mass Spectrom       Date:  2000-08       Impact factor: 3.109

2.  The role of acidic residues and of sodium ion adduction on the gas-phase H/D exchange of peptides and peptide dimers.

Authors:  John C Jurchen; Russell E Cooper; Evan R Williams
Journal:  J Am Soc Mass Spectrom       Date:  2003-12       Impact factor: 3.109

3.  Further studies on the origins of asymmetric charge partitioning in protein homodimers.

Authors:  John C Jurchen; David E Garcia; Evan R Williams
Journal:  J Am Soc Mass Spectrom       Date:  2004-10       Impact factor: 3.109

4.  High-order structure and dissociation of gaseous peptide aggregates that are hidden in mass spectra.

Authors:  A E Counterman; S J Valentine; C A Srebalus; S C Henderson; C S Hoaglund; D E Clemmer
Journal:  J Am Soc Mass Spectrom       Date:  1998-08       Impact factor: 3.109

  4 in total

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