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通过13C非共振旋转框架自旋晶格弛豫评估溶液中蛋白质的重定向扩散:各向异性翻滚的影响。

Assessment of protein reorientational diffusion in solution by 13C off-resonance rotating frame spin-lattice relaxation: effect of anisotropic tumbling.

作者信息

Morgan C F, Schleich T, Caines G H, Michael D

机构信息

Department of Chemistry, University of California, Santa Cruz 95064.

出版信息

Biopolymers. 1990 Feb 15;29(3):469-80. doi: 10.1002/bip.360290302.

Abstract

The 13C off-resonance rotating frame spin-lattice relaxation technique is applicable to the study of protein rotational diffusion behavior 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.

摘要

13C 非共振旋转框架自旋 - 晶格弛豫技术适用于在各种实验情况下研究蛋白质的旋转扩散行为。James及其同事(1978年)(《美国化学会志》100, 3590 - 3594)的原始形式体系受到随机各向同性重取向运动假设的限制。在此,我们在形式体系中纳入了各向异性翻滚,并给出了计算机模拟结果,这些结果说明了非共振旋转框架自旋 - 晶格弛豫实验中各向异性和各向同性重取向运动之间的差异。此外,我们还将肽羰基碳的化学位移各向异性作为额外的弛豫机制贡献纳入其中,以实现高场核磁共振蛋白质旋转扩散测量。

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