Zhang Hong, Shi Xiaoqing, Pelech Steven
Kinexus Bioinformatics Corporation, Suite 1, 8755 Ash Street, Vancouver, British Columbia, Canada, V6P 6T3.
Department of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
Methods Mol Biol. 2016;1360:107-22. doi: 10.1007/978-1-4939-3073-9_9.
Fuelled by advances in our understanding of the human kinome and phosphoproteome and the increasing availability of pan- and phosphosite-specific antibodies, antibody microarrays have emerged as powerful tools for interrogating protein phosphorylation-mediated signaling systems in ex vivo studies. This economical platform permits ultra-sensitive, semiquantitative measurements of the levels of hundreds of protein kinases and their substrates along with their phosphorylation status simultaneously with minute amounts of specimens. Recent technological innovations in the design and fabrication of antibody microarrays and sample preparation have permitted further refinements of the technology to yield improvements in data quality. In this chapter, we describe a detailed protocol that we have developed for tracking the expression and phosphorylation of protein kinases and their substrates in crude cell lysate samples using a high-content antibody microarray.
随着我们对人类激酶组和磷酸化蛋白质组认识的不断进步,以及泛位点和磷酸化位点特异性抗体的可得性日益增加,抗体微阵列已成为离体研究中用于探究蛋白质磷酸化介导的信号系统的强大工具。这个经济的平台允许使用微量样本同时对数百种蛋白激酶及其底物的水平以及它们的磷酸化状态进行超灵敏、半定量测量。抗体微阵列设计与制造以及样品制备方面的最新技术创新使该技术得以进一步完善,从而提高了数据质量。在本章中,我们描述了一个详细的方案,该方案是我们利用高内涵抗体微阵列跟踪粗细胞裂解物样本中蛋白激酶及其底物的表达和磷酸化而开发的。