Life Sciences Institute and the Departments of Pharmacology and Biological Sciences, University of Michigan, Ann Arbor, MI 48109, United States.
Life Sciences Institute and the Departments of Pharmacology and Biological Sciences, University of Michigan, Ann Arbor, MI 48109, United States.
Curr Opin Cell Biol. 2014 Apr;27:25-31. doi: 10.1016/j.ceb.2013.10.009. Epub 2013 Nov 26.
The atomic structure of a protein can greatly advance our understanding of molecular recognition and catalysis, properties of fundamental importance in signal transduction. However, a single structure is incapable of fully describing how a protein functions, particularly when allostery is involved. Recent advances in the structure and function of G protein-coupled receptor (GPCR) kinases (GRKs) have concentrated on the mechanism of their inhibition by small and large molecules. These studies have generated a wealth of new information on the conformational flexibility of these enzymes, which opens new avenues for the development of selective chemical probes and provides deeper insights into the molecular basis for activation of these enzymes by GPCRs and phospholipids.
蛋白质的原子结构可以极大地促进我们对分子识别和催化的理解,这些性质在信号转导中至关重要。然而,单一结构并不能完全描述蛋白质的功能,特别是在涉及变构的情况下。近年来,G 蛋白偶联受体激酶(GRKs)的结构和功能的研究集中在小分子和大分子抑制它们的机制上。这些研究为这些酶的构象灵活性提供了丰富的新信息,为选择性化学探针的开发开辟了新途径,并深入了解了 GPCR 和磷脂激活这些酶的分子基础。