ASSESSMENT OF PROTEIN REORIENTATIONAL DIFFUSION IN SOLUTION BY C-13 OFF-RESONANCE ROTATING FRAME SPIN-LATTICE RELAXATION - EFFECT OF ANISOTROPIC TUMBLING

被引:6
作者
MORGAN, CF
SCHLEICH, T
CAINES, GH
MICHAEL, D
机构
[1] Department of Chemistry, University of California, Santa Cruz, California
[2] CIBA VISON, Alpharetta, Georgia, 30201
关键词
D O I
10.1002/bip.360290302
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
The 13C off‐resonance rotating frame spin‐lattice relaxation technique is applicable to the study of protien rotational diffusion behaviour in a variety of experimental situations. The original formalism of James and co‐workers (1978) (J. Amer. Chem. Soc. 100, 3590–3594) was constrained by the assumption of random isotropic reorientational motion. Here we include in the formalism anisotropic tumbling, and present the results of computer simulations illustrating the differences between anisotropic and isotropic reorientational motion for the off‐resonance rotating frame spin–lattice relaxation experiment. In addition, We have included chemical shift anisotropy of the peptide carbonyl carbon as an additional relaxation mechanism contribution, to permit high field nmr protein rotational diffusion measurements. Copyright © 1990 John Wiley & Sons, Inc.
引用
收藏
页码:469 / 480
页数:12
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