An improved method for suppressing protein background in PFG NMR experiments to determine ligand diffusion coefficients in the presence of receptor

被引:9
作者
Becker, Bridget A.
Morris, Kevin F.
Larive, Cynthia K.
机构
[1] Univ Calif Riverside, Dept Chem, Riverside, CA 92521 USA
[2] Carthage Coll, Dept Chem, Kenosha, WI 53140 USA
关键词
diffusion; PFG NMR; PGSE NMR; ALPHA(1)-ACID GLYCOPROTEIN; BINDING; SPECTROSCOPY; GRADIENT;
D O I
10.1016/j.jmr.2006.04.010
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In NMR diffusion experiments to study ligand-protein binding equilibria, the spectral background due to broad protein resonances can contribute significantly to the measured ligand signal intensity resulting in erroneous binding affinities. One method to suppress the protein spectral background involves coupling a CPMG pulse train before or after the BPPSTE pulse sequence to allow for differential T, relaxation of the broad protein resonances. Here, we present an improved method, the Gradient Phase Encoded Spin-lock (GraPES) experiment that integrates the relaxation filter into the diffusion period. Compared with sequential CPMG-BPPSTE pulse sequences, GraPES offers effective suppression of the protein background with improved signal-to-noise ratios and shorter experiment times. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:327 / 330
页数:4
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