NMR studies of ligand binding

被引:39
|
作者
Nitsche, Christoph [1 ]
Otting, Gottfried [1 ]
机构
[1] Australian Natl Univ, Res Sch Chem, Canberra, ACT 2601, Australia
基金
澳大利亚研究理事会;
关键词
PARAMAGNETIC RELAXATION ENHANCEMENT; VIRUS NS2B-NS3 PROTEASE; SOLID-STATE NMR; PSEUDOCONTACT SHIFTS; DRUG DISCOVERY; LEAD DISCOVERY; CHEMICAL-SHIFT; SPECTROSCOPY; COMPLEXES; PROTEINS;
D O I
10.1016/j.sbi.2017.09.001
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
NMR spectroscopy is an established tool in drug discovery, but its strength is commonly regarded to be largely confined to the early stages of hit discovery and fragment based drug design, where NMR offers unique capabilities of characterizing the binding modes of ligand molecules that bind sufficiently weakly to be in rapid exchange between bound and free state. Here we, first, provide a meta-review of recent reviews on NMR studies of ligand binding and, second, review recent progress towards NMR characterization of the ligand binding mode in stable protein-ligand complexes, with particular emphasis on the global positioning system (GPS) approach enabled by paramagnetic lanthanide tags.
引用
收藏
页码:16 / 22
页数:7
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