Segmental charge distributions of Cytochrome c on transfer into the gas phase

被引:10
作者
Breuker, K.
机构
[1] Univ Innsbruck, Inst Organ Chem, A-6020 Innsbruck, Austria
[2] Univ Innsbruck, CMBI, A-6020 Innsbruck, Austria
基金
美国国家卫生研究院;
关键词
electrospray ionization; proton transfer;
D O I
10.1016/j.ijms.2006.04.004
中图分类号
O64 [物理化学(理论化学)、化学物理学]; O56 [分子物理学、原子物理学];
学科分类号
070203 ; 070304 ; 081704 ; 1406 ;
摘要
Segmental charge distributions of Cytochrome c ions in the transition from solution to gas phase are studied by native electron capture dissociation (NECD). The data suggest that the solution charge distribution of native Cytochrome c is partially preserved during the electrospray ionization process. Segments with charge values different from those in solution correspond to protein regions that are the first to unfold on transfer into the gas phase, consistent with an increased gas phase basicity of. and facile proton transfer to. the newly exposed sites. Changes in the charge distribution at elevated temperatures indicate further unfolding, as well as proton transfer as a result of the increased electrostatic interactions in a gas phase environment. (C) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:249 / 255
页数:7
相关论文
共 44 条
[1]   Evidence for unfolding and refolding of gas-phase cytochrome c ions in a Paul trap [J].
Badman, ER ;
Myung, S ;
Clemmer, DE .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 2005, 16 (09) :1493-1497
[2]   Solution structure of oxidized horse heart cytochrome c [J].
Banci, L ;
Bertini, I ;
Gray, HB ;
Luchinat, C ;
Reddig, T ;
Rosato, A ;
Turano, P .
BIOCHEMISTRY, 1997, 36 (32) :9867-9877
[3]   The thermal unfolding of native cytochrome c in the transition from solution to gas phase probed by native electron capture dissociation [J].
Breuker, K ;
McLafferty, FW .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2005, 44 (31) :4911-4914
[4]   Detailed unfolding and folding of gaseous ubiquitin ions characterized by electron capture dissociation [J].
Breuker, K ;
Oh, HB ;
Horn, DM ;
Cerda, BA ;
McLafferty, FW .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (22) :6407-6420
[5]   Nonergodic and conformational control of the electron capture dissociation of protein cations [J].
Breuker, K ;
Oh, HB ;
Lin, C ;
Carpenter, BK ;
McLafferty, FW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (39) :14011-14016
[6]   Native electron capture dissociation for the structural characterization of noncovalent interactions in native cytochrome c [J].
Breuker, K ;
McLafferty, FW .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2003, 42 (40) :4900-4904
[7]   PROBING CONFORMATIONAL-CHANGES IN PROTEINS BY MASS-SPECTROMETRY [J].
CHOWDHURY, SK ;
KATTA, V ;
CHAIT, BT .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1990, 112 (24) :9012-9013
[8]   NAKED PROTEIN CONFORMATIONS - CYTOCHROME-C IN THE GAS-PHASE [J].
CLEMMER, DE ;
HUDGINS, RR ;
JARROLD, MF .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1995, 117 (40) :10141-10142
[9]   BIRD (blackbody infrared radiative dissociation): Evolution, principles, and applications [J].
Dunbar, RC .
MASS SPECTROMETRY REVIEWS, 2004, 23 (02) :127-158
[10]   Origin and number of charges observed on multiply-protonated native proteins produced by ESI [J].
Felitsyn, N ;
Peschke, M ;
Kebarle, P .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY, 2002, 219 (01) :39-62