Selective transient heteronuclear cross relaxation in a selectively C-13(alpha)-labeled peptide

被引:2
作者
Allard, P
Jarvet, J
Graslund, A
机构
[1] UNIV STOCKHOLM,ARRHENIUS LABS,DEPT BIOPHYS,S-10691 STOCKHOLM,SWEDEN
[2] KAROLINSKA INST,NOVUM,CTR STRUCT BIOCHEM,S-14157 HUDDINGE,SWEDEN
[3] ROYAL INST TECHNOL,NOVUM,S-14157 HUDDINGE,SWEDEN
关键词
NUCLEAR-MAGNETIC-RESONANCE; PULSED-FIELD GRADIENTS; MODEL-FREE APPROACH; SPIN-DIFFUSION; SENSITIVITY IMPROVEMENT; NMR; MACROMOLECULES; SPECTRA; SPECTROSCOPY; ELIMINATION;
D O I
10.1006/jmre.1996.7478
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A new pulse sequence for the direct measurement of heteronuclear cross-relaxation rates is presented. The pulse sequence uses proton detection of transient carbon magnetization with sensitivity-enhanced transfer of magnetization and pulsed held gradients for coherence selection and water suppression. The heteronuclear cross-relaxation rate is measured using either nonselective or selective inversion of all or particular protons. A technique for the suppression of spin diffusion is also applied. The pulse sequence is tested on a peptide with a selectively C-13-labeled alpha-carbon. The directly measured rate is compared with and agrees well with the cross-relaxation rates as traditionally calculated from the steady-state NOE and carbon longitudinal-relaxation rate. (C) 1997 Academic Press.
引用
收藏
页码:97 / 103
页数:7
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