Literature DB >> 17129173

Intermolecular interactions in biomolecular systems examined by mass spectrometry.

Thomas Wyttenbach1, Michael T Bowers.   

Abstract

With the development of electrospray and matrix-assisted laser desorption ionization, mass spectrometry (MS) evolved into a powerful tool in the field of biochemistry. Whereas MS is primarily analytical in nature, an increasing number of MS research groups employ the method to address fundamental biochemical questions. Probing the interaction of noncovalently bound molecules in the mass spectrometer is one of the most interesting MS-based experiments possible today, with the potential of making a significant contribution to the basic understanding of the structure and function of biochemical complexes. Here we review a number of current research efforts employing primarily MS techniques to investigate intermolecular interactions in biochemical systems. Examples chosen include the interaction of biomolecules with solvent molecules; interactions between nucleic-acid molecules, in particular, interactions in duplex and quadruplex structures; and interactions between proteins involved in neurodegenerative diseases. Finally we conclude by presenting a few examples of very large biomolecular assemblies in the mega-Dalton range analyzed by MS.

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Year:  2007        PMID: 17129173     DOI: 10.1146/annurev.physchem.58.032806.104515

Source DB:  PubMed          Journal:  Annu Rev Phys Chem        ISSN: 0066-426X            Impact factor:   12.703


  32 in total

1.  Solution and gas-phase H/D exchange of protein-small-molecule complexes: Cex and its inhibitors.

Authors:  Yang Kang; Peran Terrier; Chuanfan Ding; D J Douglas
Journal:  J Am Soc Mass Spectrom       Date:  2011-10-18       Impact factor: 3.109

2.  Mapping a noncovalent protein-peptide interface by top-down FTICR mass spectrometry using electron capture dissociation.

Authors:  David J Clarke; Euan Murray; Ted Hupp; C Logan Mackay; Pat R R Langridge-Smith
Journal:  J Am Soc Mass Spectrom       Date:  2011-05-11       Impact factor: 3.109

3.  Ion mobility-mass spectrometry reveals conformational changes in charge reduced multiprotein complexes.

Authors:  Russell E Bornschein; Suk-Joon Hyung; Brandon T Ruotolo
Journal:  J Am Soc Mass Spectrom       Date:  2011-07-16       Impact factor: 3.109

4.  Pseudorandom sequence modifications for ion mobility orthogonal time-of-flight mass spectrometry.

Authors:  Brian H Clowers; Mikhail E Belov; David C Prior; William F Danielson; Yehia Ibrahim; Richard D Smith
Journal:  Anal Chem       Date:  2008-03-01       Impact factor: 6.986

5.  Collisional activation of protein complexes: picking up the pieces.

Authors:  Justin L P Benesch
Journal:  J Am Soc Mass Spectrom       Date:  2008-11-27       Impact factor: 3.109

Review 6.  Integrating mass spectrometry of intact protein complexes into structural proteomics.

Authors:  Suk-Joon Hyung; Brandon T Ruotolo
Journal:  Proteomics       Date:  2012-05       Impact factor: 3.984

7.  Hydration energies of deprotonated amino acids from gas phase equilibria measurements.

Authors:  Henryk Wincel
Journal:  J Am Soc Mass Spectrom       Date:  2008-05-28       Impact factor: 3.109

8.  Biological chemistry: Dehydrated but unharmed.

Authors:  Justin L P Benesch; Carol V Robinson
Journal:  Nature       Date:  2009-12-03       Impact factor: 49.962

9.  Traveling-wave Ion Mobility-Mass Spectrometry Reveals Additional Mechanistic Details in the Stabilization of Protein Complex Ions through Tuned Salt Additives.

Authors:  Linjie Han; Brandon T Ruotolo
Journal:  Int J Ion Mobil Spectrom       Date:  2013-01-29

10.  On the zwitterionic nature of gas-phase peptides and protein ions.

Authors:  Roberto Marchese; Rita Grandori; Paolo Carloni; Simone Raugei
Journal:  PLoS Comput Biol       Date:  2010-05-06       Impact factor: 4.475

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