Boyle Scott N, Koleske Anthony J
Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, CT 06520, United States.
Drug Discov Today. 2007 Sep;12(17-18):717-24. doi: 10.1016/j.drudis.2007.07.019. Epub 2007 Aug 23.
Aberrant protein kinase signaling is a hallmark of many human diseases including cancer, diabetes, and neurological disorders. Kinase inhibitors have shown to be successful at treating some of these diseases, implying that understanding kinase signaling pathways may lead to additional, non-kinase drug targets. However, identifying substrates of protein kinases is difficult due to the universality of the chemical mechanism kinases utilize and the ability of multiple kinases to phosphorylate the same protein substrates. In this review, we explore the advantages and disadvantages of several techniques for identifying kinase substrates. Once putative substrates are identified, their validation as physiological substrates remains a major challenge. We propose three criteria for confirming the physiological relevance of a putative substrate's interaction with a kinase.
异常的蛋白激酶信号传导是包括癌症、糖尿病和神经疾病在内的许多人类疾病的一个标志。激酶抑制剂已被证明在治疗其中一些疾病方面取得了成功,这意味着了解激酶信号通路可能会带来其他非激酶药物靶点。然而,由于激酶利用的化学机制具有普遍性,且多种激酶能够磷酸化相同的蛋白质底物,因此鉴定蛋白激酶的底物很困难。在本综述中,我们探讨了几种用于鉴定激酶底物的技术的优缺点。一旦确定了假定的底物,将其验证为生理底物仍然是一项重大挑战。我们提出了三个标准来确认假定底物与激酶相互作用的生理相关性。