Studies on ligand binding to histidine triad nucleotide binding protein 1

被引:9
|
作者
Bai, Guoyun [1 ]
Feng, Bo [1 ]
Wang, Jia Bei [1 ]
Pozharski, Edwin [1 ]
Shapiro, Michael [1 ]
机构
[1] Univ Maryland, Dept Pharmaceut Sci, Baltimore, MD 21201 USA
关键词
NMR; HINT1; Ligand-protein interactions; HSQC chemical shift mapping; INTERACTIVE PROTEIN; FAMILY; KINASE; SCHIZOPHRENIA; EXPRESSION; DOMAIN; MEMBER; GENE; FHIT;
D O I
10.1016/j.bmc.2010.07.051
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
Histidine triad nucleotide binding protein (HINT1) is an intracellular protein that binds purine mononucleotides. Strong sequence conservation suggests that these proteins play a fundamental role in cell biology, however its exact cellular function continues to remain elusive. nuclear magnetic resonance (NMR) studies using STD and HSQC were conducted to observe ligand binding to HINT1. These studies were confirmed using fluorescence spectroscopy titrations. We found that AICAR, the first non-phosphate containing ligand, binds to mouse histidine triad nucleotide binding protein 1 (HINT1). Chemical shift perturbations are mapped onto the X-ray structure showing AICAR binds at the same site as GMP. The NMR results demonstrated that this method will be valuable for the future screening of small molecules that can be used to modulate the function of HINT1. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6756 / 6762
页数:7
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