The global analysis of DEER data

被引:75
作者
Brandon, Suzanne [1 ]
Beth, Albert H. [1 ]
Hustedt, Eric J. [1 ]
机构
[1] Vanderbilt Univ, Dept Mol Physiol & Biophys, Nashville, TN 37232 USA
关键词
DEER; PELDOR; Global analysis; ELECTRON DOUBLE-RESONANCE; CYTOPLASMIC DOMAIN; ERYTHROCYTE BAND-3; SPIN-LABELS; PROTEIN; SPECTROSCOPY; ORIENTATION; DISTANCES; RADICALS; PELDOR;
D O I
10.1016/j.jmr.2012.03.006
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Double Electron-Electron Resonance (DEER) has emerged as a powerful technique for measuring long range distances and distance distributions between paramagnetic centers in biomolecules. This information can then be used to characterize functionally relevant structural and dynamic properties of biological molecules and their macromolecular assemblies. Approaches have been developed for analyzing experimental data from standard four-pulse DEER experiments to extract distance distributions. However, these methods typically use an a priori baseline correction to account for background signals. In the current work an approach is described for direct fitting of the DEER signal using a model for the distance distribution which permits a rigorous error analysis of the fitting parameters. Moreover, this approach does not require a priori background correction of the experimental data and can take into account excluded volume effects on the background signal when necessary. The global analysis of multiple DEER data sets is also demonstrated. Global analysis has the potential to provide new capabilities for extracting distance distributions and additional structural parameters in a wide range of studies. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:93 / 104
页数:12
相关论文
共 41 条
[1]   High-resolution distance mapping in rhodopsin reveals the pattern of helix movement due to activation [J].
Altenbach, Christian ;
Kusnetzow, Ana Karin ;
Ernst, Oliver P. ;
Hofmann, Klaus Peter ;
Hubbell, Wayne L. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (21) :7439-7444
[2]  
APPELL KC, 1981, J BIOL CHEM, V256, P1104
[3]  
BEECHEM JM, 1992, METHOD ENZYMOL, V210, P37
[4]   Monitoring Inhibitor-Induced Conformational Population Shifts in HIV-1 Protease by Pulsed EPR Spectroscopy [J].
Blackburn, Mandy E. ;
Veloro, Angelo M. ;
Fanucci, Gail E. .
BIOCHEMISTRY, 2009, 48 (37) :8765-8767
[5]   Protein structure determination using long-distance constraints from double-quantum coherence ESR: Study of T4 lysozyme [J].
Borbat, PP ;
Mchaourab, HS ;
Freed, JH .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (19) :5304-5314
[6]   Visualization of distance distribution from pulsed double electron-electron resonance data [J].
Bowman, MK ;
Maryasov, AG ;
Kim, N ;
DeRose, VJ .
APPLIED MAGNETIC RESONANCE, 2004, 26 (1-2) :23-39
[7]   The determination of pair distance distributions by pulsed ESR using Tikhonov regularization [J].
Chiang, YW ;
Borbat, PP ;
Freed, JH .
JOURNAL OF MAGNETIC RESONANCE, 2005, 172 (02) :279-295
[8]   Ion/substrate-dependent conformational dynamics of a bacterial homolog of neurotransmitter: sodium symporters [J].
Claxton, Derek P. ;
Quick, Matthias ;
Shi, Lei ;
de Carvalho, Fernanda Delmondes ;
Weinstein, Harel ;
Javitch, Jonathan A. ;
Mchaourab, Hassane S. .
NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2010, 17 (07) :822-U68
[9]   High-field pulsed electron-electron double resonance spectroscopy to determine the orientation of the tyrosyl radicals in ribonucleotide reductase [J].
Denysenkov, V. P. ;
Prisner, T. F. ;
Stubbe, J. ;
Bennati, M. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (36) :13386-13390
[10]   Pulsed Electron-Electron Double-Resonance Determination of Spin-Label Distances and Orientations on the Tetrameric Potassium Ion Channel KcsA [J].
Endeward, Burkhard ;
Butterwick, Joel A. ;
MacKinnon, Roderick ;
Prisner, Thomas F. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2009, 131 (42) :15246-15250