13C spin relaxation measurements in RNA:: Sensitivity and resolution improvement using spin-state selective correlation experiments

被引:42
作者
Boisbouvier, J [1 ]
Brutscher, B [1 ]
Simorre, JP [1 ]
Marion, D [1 ]
机构
[1] CEA, CNRS, Inst Biol Struct Jean Pierre Ebel, F-38027 Grenoble, France
关键词
C-13; relaxation; conformational exchange; cross correlation; CSA; nucleic acids; TROSY;
D O I
10.1023/A:1008365712799
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
A set of new NMR pulse sequences has been designed for the measurement of C-13 relaxation rate constants in RNA and DNA bases: the spin-lattice relaxation rate constant R(C-z), the spin-spin relaxation rate constant R(C+), and the CSA-dipolar cross-correlated relaxation rate constant Gamma(C,CH)(xy). The use of spin-state selective correlation techniques provides increased sensitivity and spectral resolution. Sensitivity optimised C-C filters are included in the pulse schemes for the suppression of signals originating from undesired carbon isotopomers. The experiments are applied to a 15% C-13-labelled 33-mer RNA-theophylline complex. The measured R(C+)/Gamma(C,CH)(xy) ratios indicate that C-13 CSA tensors do not vary significantly for the same type of carbon (C-2, C-6, C-8), but that they differ from one type to another. In addition, conformational exchange effects in the RNA bases are detected as a change in the relaxation decay of the narrow C-13 doublet component when varying the spacing of a CPMG pulse train. This new approach allows the detection of small exchange effects with a higher precision compared to conventional techniques.
引用
收藏
页码:241 / 252
页数:12
相关论文
共 47 条
[1]  
Akke M, 1997, RNA, V3, P702
[2]   Monitoring macromolecular motions on microsecond to millisecond time scales by R(1)rho-R(1) constant relaxation time NMR spectroscopy [J].
Akke, M ;
Palmer, AG .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1996, 118 (04) :911-912
[3]   An α/β-HSQC-α/β experiment for spin-state selective editing of IS cross peaks [J].
Andersson, P ;
Annila, A ;
Otting, G .
JOURNAL OF MAGNETIC RESONANCE, 1998, 133 (02) :364-367
[4]   SPIN ECHOES AND CHEMICAL EXCHANGE [J].
BLOOM, M ;
REEVES, LW ;
WELLS, EJ .
JOURNAL OF CHEMICAL PHYSICS, 1965, 42 (05) :1615-&
[5]   C-13-NMR RELAXATION IN 3 DNA OLIGONUCLEOTIDE DUPLEXES - MODEL-FREE ANALYSIS OF INTERNAL AND OVERALL MOTION [J].
BORER, PN ;
LAPLANTE, SR ;
KUMAR, A ;
ZANATTA, N ;
MARTIN, A ;
HAKKINEN, A ;
LEVY, GC .
BIOCHEMISTRY, 1994, 33 (09) :2441-2450
[6]   Backbone dynamics and structural characterization of the partially folded A state of ubiquitin by H-1, C-13, and N-15 nuclear magnetic resonance spectroscopy [J].
Brutscher, B ;
Bruschweiler, R ;
Ernst, RR .
BIOCHEMISTRY, 1997, 36 (42) :13043-13053
[7]   Improved sensitivity and resolution in 1H-13C NMR experiments of RNA [J].
Brutscher, B ;
Boisbouvier, J ;
Pardi, A ;
Marion, D ;
Simorre, JP .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1998, 120 (46) :11845-11851
[8]   Crystal structure of a group I ribozyme domain: Principles of RNA packing [J].
Cate, JH ;
Gooding, AR ;
Podell, E ;
Zhou, KH ;
Golden, BL ;
Kundrot, CE ;
Cech, TR ;
Doudna, JA .
SCIENCE, 1996, 273 (5282) :1678-1685
[9]  
Cavanagh J., 1996, PROTEIN NMR SPECTROS
[10]   A doublet-separated sensitivity-enhanced HSQC for the determination of scalar and dipolar one-bond J-couplings [J].
Cordier, F ;
Dingley, AJ ;
Grzesiek, S .
JOURNAL OF BIOMOLECULAR NMR, 1999, 13 (02) :175-180