On the measurement of 15N-{1H} nuclear Overhauser effects

被引:32
作者
Ferrage, Fabien [1 ,2 ]
Piserchio, Andrea [2 ,3 ]
Cowburn, David [2 ]
Ghose, Ranajeet [3 ,4 ]
机构
[1] Ecole Normale Super, CNRS, UMR 8642, Dept Chim, F-75231 Paris 05, France
[2] New York Struct Biol Ctr, New York, NY 10027 USA
[3] CUNY City Coll, Dept Chem, New York, NY 10031 USA
[4] CUNY, Grad Ctr, New York, NY 10016 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
cross-relaxation; nuclear Overhauser effect; Average Liouvillian Theory; biomolecular dynamics; protein dynamics;
D O I
10.1016/j.jmr.2008.03.011
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Accurate quantification of the N-15-{H-1}steady-state NOE is central to current methods for the elucidation of protein backbone dynamics on the fast, sub-nanosecond time scale. This experiment is highly susceptible to systematic errors arising from multiple sources. The nature of these errors and their effects on the determined NOE ratio is evaluated by a detailed analysis of the spin dynamics during the pair of experiments used to measure this ratio and possible improvements suggested. The experiment that includes 1H irradiation, is analyzed in the framework of Average Liouvillian Theory and a modified saturation scheme that generates a stable steady-state and eliminates the need to completely saturate H-1 nuclei is presented. The largest source of error, however, in H-1-dilute systems at ultra-high fields is found to be an overestimation of the steady-state NOE value as a consequence of the incomplete equilibration of the magnetization in the so-called "reference experiment". The use of very long relaxation delays is usually an effective, but time consuming, solution. Here, we introduce an alternative reference experiment, designed for larger, deuterated systems, that uses the fastest relaxing component of the longitudinal magnetization as a closer approximation to the equilibrium state for shorter relaxation delays. The utility of the modified approach is illustrated through simulations on realistic spin systems over a wide range of time scales and experimentally verified using a perdeuterated sample of human ubiquitin. (c) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:302 / 313
页数:12
相关论文
共 38 条
[1]   RELAXATION EFFECTS IN NUCLEAR MAGNETIC RESONANCE ABSORPTION [J].
BLOEMBERGEN, N ;
PURCELL, EM ;
POUND, RV .
PHYSICAL REVIEW, 1948, 73 (07) :679-712
[2]   Measurement of 15N relaxation in the detergent-solubilized tetrameric KcsA potassium channel [J].
Chill, Jordan H. ;
Louis, John M. ;
Baber, James L. ;
Bax, Ad .
JOURNAL OF BIOMOLECULAR NMR, 2006, 36 (02) :123-136
[3]   DEVIATIONS FROM THE SIMPLE 2-PARAMETER MODEL-FREE APPROACH TO THE INTERPRETATION OF N-15 NUCLEAR MAGNETIC-RELAXATION OF PROTEINS [J].
CLORE, GM ;
SZABO, A ;
BAX, A ;
KAY, LE ;
DRISCOLL, PC ;
GRONENBORN, AM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1990, 112 (12) :4989-4991
[4]   SPECTRAL DENSITY-FUNCTION MAPPING USING N-15 RELAXATION DATA EXCLUSIVELY [J].
FARROW, NA ;
ZHANG, OW ;
SZABO, A ;
TORCHIA, DA ;
KAY, LE .
JOURNAL OF BIOMOLECULAR NMR, 1995, 6 (02) :153-162
[5]   THEORY OF THE ROTATIONAL BROWNIAN MOTION OF A FREE RIGID BODY [J].
FAVRO, LD .
PHYSICAL REVIEW, 1960, 119 (01) :53-62
[6]   Highly selective excitation in biomolecular NMR by frequency-switched single-transition cross-polarization [J].
Ferrage, F ;
Eykyn, TR ;
Bodenhausen, G .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (10) :2076-2077
[7]   An approach to direct determination of protein dynamics from 15N NMR relaxation at multiple fields, independent of variable 15N chemical shift anisotropy and chemical exchange contributions [J].
Fushman, D ;
Tjandra, N ;
Cowburn, D .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (37) :8577-8582
[8]   The main-chain dynamics of the dynamin pleckstrin homology (PH) domain in solution: Analysis of N-15 relaxation with monomer/dimer equilibration [J].
Fushman, D ;
Cahill, S ;
Cowburn, D .
JOURNAL OF MOLECULAR BIOLOGY, 1997, 266 (01) :173-194
[9]   The use of 2H, 13C, 15N multidimensional NMR to study the structure and dynamics of proteins [J].
Gardner, KH ;
Kay, LE .
ANNUAL REVIEW OF BIOPHYSICS AND BIOMOLECULAR STRUCTURE, 1998, 27 :357-406
[10]   Determination of the rotational diffusion tensor of macromolecules in solution from NMR relaxation data with a combination of exact and approximate methods - Application to the determination of interdomain orientation in multidomain proteins [J].
Ghose, R ;
Fushman, D ;
Cowburn, D .
JOURNAL OF MAGNETIC RESONANCE, 2001, 149 (02) :204-217