Cox Eric, Uzoma Ijeoma, Guzzo Catherine, Jeong Jun Seop, Matunis Michael, Blackshaw Seth, Zhu Heng
Biochemistry, Cellular and Molecular Biology Graduate Program, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Methods Mol Biol. 2015;1295:455-63. doi: 10.1007/978-1-4939-2550-6_32.
The functional protein microarray is a powerful and versatile systems biology and proteomics tool that allows the rapid activity profiling of thousands of proteins in parallel. We have recently developed a human proteome array, the HuProt array, which includes ~80 % of all the full-length proteins of the human proteome. In one recent application of the HuProt array, we identified numerous SUMO E3 ligase-dependent SUMOylation substrates. For many SUMO E3 ligases, only a small number of substrates have been identified and the target specificities of these ligases therefore remain poorly defined. In this protocol, we outline a method we developed using the HuProt array to screen the human proteome to identify novel SUMO E3 ligase substrates recognized by specific E3 ligases.
功能蛋白质微阵列是一种强大且通用的系统生物学和蛋白质组学工具,可实现数千种蛋白质的并行快速活性分析。我们最近开发了一种人类蛋白质组阵列,即HuProt阵列,它包含了人类蛋白质组中约80%的全长蛋白质。在HuProt阵列的一项最新应用中,我们鉴定出了众多依赖于SUMO E3连接酶的SUMO化底物。对于许多SUMO E3连接酶而言,仅鉴定出了少数底物,因此这些连接酶的靶标特异性仍不清楚。在本方案中,我们概述了一种利用HuProt阵列开发的方法,用于筛选人类蛋白质组,以鉴定由特定E3连接酶识别的新型SUMO E3连接酶底物。