Schaller Michael D
Lineberger Comprehensive Cancer Center, Carolina Cardiovascular Biology Center, Comprehensive Center for Inflammatory Disorders, 534 Taylor Hall, CB 7090, University of North Carolina, Chapel Hill, NC 5799, USA. email
Biochem J. 2008 Mar 15;410(3):e3-4. doi: 10.1042/BJ20080133.
Pyk2 (proline-rich tyrosine kinase 2) and FAK (focal adhesion kinase) are highly related tyrosine kinases. One distinguishing feature is the differential regulation of the two enzymes in response to elevation of cytoplasmic calcium. In the latest issue of the Biochemical Journal, Sasaki and co-workers have provided insight into the calcium-dependent regulation of Pyk2. The findings suggest that calmodulin may bind the FERM (4.1/ezrin/radixin/moesin) domain to promote Pyk2 activation in response to calcium signals triggered by vasopressin. While the molecular details of the protein-protein interaction and mechanism of activation remain to be firmly established, this study is the first to provide mechanistic insight into the regulation of Pyk2 by calcium.
富含脯氨酸的酪氨酸激酶2(Pyk2)和粘着斑激酶(FAK)是高度相关的酪氨酸激酶。一个显著特征是这两种酶在细胞质钙升高时受到不同的调节。在最新一期的《生物化学杂志》上,佐佐木及其同事深入探讨了Pyk2的钙依赖性调节。研究结果表明,钙调蛋白可能与4.1/埃兹蛋白/根蛋白/膜突蛋白(FERM)结构域结合,以促进Pyk2在血管加压素触发的钙信号响应中被激活。虽然蛋白质-蛋白质相互作用的分子细节和激活机制仍有待确切确定,但这项研究首次为钙对Pyk2的调节提供了机制上的见解。