Oxidative Protein Labeling with Analysis by Mass Spectrometry for the Study of Structure, Folding, and Dynamics

被引:6
作者
Liuni, Peter [1 ]
Zhu, Shaolong [1 ]
Wilson, Derek J. [1 ,2 ]
机构
[1] York Univ, Dept Chem, Toronto, ON M3J 1P3, Canada
[2] York Univ, Ctr Res Mass Spectrometry, Toronto, ON M3J 1P3, Canada
关键词
ELECTRON-CAPTURE DISSOCIATION; FAST PHOTOCHEMICAL OXIDATION; NUCLEAR-MAGNETIC-RESONANCE; SINGLE-RESIDUE RESOLUTION; INTEGRAL MEMBRANE-PROTEIN; HUMAN APOLIPOPROTEIN-E; BINDING SITES; CONFORMATIONAL-CHANGES; HYDROGEN-EXCHANGE; CRYSTAL-STRUCTURE;
D O I
10.1089/ars.2014.5850
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Significance: Analytical approaches that can provide insights into the mechanistic processes underlying protein folding and dynamics are few since the target analytes-high-energy structural intermediates-are short lived and often difficult to distinguish from coexisting structures. Folding "intermediates'' can be populated at equilibrium using weakly denaturing solvents, but it is not clear that these species are identical to those that are transiently populated during folding under "native'' conditions. Oxidative labeling with mass spectrometric analysis is a powerful alternative for structural characterization of proteins and transient protein species based on solvent exposure at specific sites. Recent Advances: Oxidative labeling is increasingly used with exceedingly short (mu s) labeling pulses, both to minimize the occurrence of artifactual structural changes due to the incorporation of label and to detect short-lived species. The recent introduction of facile photolytic approaches for producing reactive oxygen species is an important technological advance that will enable more widespread adoption of the technique. Critical Issues: The most common critique of oxidative labeling data is that even with brief labeling pulses, covalent modification of the protein may cause significant artifactual structural changes. Future Directions: While the oxidative labeling with the analysis by mass spectrometry is mature enough that most basic methodological issues have been addressed, a complete systematic understanding of side chain reactivity in the context of intact proteins is an avenue for future work. Specifically, there remain issues around the impact of primary sequence and side chain interactions on the reactivity of "solvent-exposed'' residues. Due to its analytical power, wide range of applications, and relative ease of implementation, oxidative labeling is an increasingly important technique in the bioanalytical toolbox.
引用
收藏
页码:497 / 510
页数:14
相关论文
共 123 条
[1]   PRINCIPLES THAT GOVERN FOLDING OF PROTEIN CHAINS [J].
ANFINSEN, CB .
SCIENCE, 1973, 181 (4096) :223-230
[2]   Nanosecond laser-induced photochemical oxidation method for protein surface mapping with mass spectrometry [J].
Aye, TT ;
Low, TY ;
Sze, SK .
ANALYTICAL CHEMISTRY, 2005, 77 (18) :5814-5822
[3]   PROTEIN-FOLDING INTERMEDIATES - NATIVE-STATE HYDROGEN-EXCHANGE [J].
BAI, YW ;
SOSNICK, TR ;
MAYNE, L ;
ENGLANDER, SW .
SCIENCE, 1995, 269 (5221) :192-197
[4]   Synchrotron protein footprinting supports substrate translocation by ClpA via ATP-induced movements of the D2 loop [J].
Bohon, Jen ;
Jennings, Laura D. ;
Phillips, Christine M. ;
Licht, Stuart ;
Chance, Mark R. .
STRUCTURE, 2008, 16 (08) :1157-1165
[5]   INTERMEDIATES IN THE FOLDING OF THE MEMBRANE-PROTEIN BACTERIORHODOPSIN [J].
BOOTH, PJ ;
FLITSCH, SL ;
STERN, LJ ;
GREENHALGH, DA ;
KIM, PS ;
KHORANA, HG .
NATURE STRUCTURAL BIOLOGY, 1995, 2 (02) :139-143
[6]   Intermediates in the assembly of bacteriorhodopsin investigated by time-resolved absorption spectroscopy [J].
Booth, PJ ;
Farooq, A .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1997, 246 (03) :674-680
[7]   Using microwave-assisted metal-catalyzed oxidation reactions and mass spectrometry to increase the rate at which the copper-binding sites of a protein are determined [J].
Bridgewater, JD ;
Vachet, RW .
ANALYTICAL CHEMISTRY, 2005, 77 (14) :4649-4653
[8]   Metal-catalyzed oxidation reactions and mass spectrometry: The roles of ascorbate and different oxidizing agents in determining Cu-protein-binding sites [J].
Bridgewater, JD ;
Vachet, RW .
ANALYTICAL BIOCHEMISTRY, 2005, 341 (01) :122-130
[9]   The effect of histidine oxidation on the dissociation patterns of peptide ions [J].
Bridgewater, Juma D. ;
Srikanth, R. ;
Lim, Jihyeon ;
Vachet, Richard W. .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 2007, 18 (03) :553-562
[10]   The crystal structure of plasma gelsolin: Implications for actin severing, capping, and nucleation [J].
Burtnick, LD ;
Koepf, EK ;
Grimes, J ;
Jones, EY ;
Stuart, DI ;
McLaughlin, PJ ;
Robinson, RC .
CELL, 1997, 90 (04) :661-670