Thiele Alexandra, Weiwad Matthias, Zerweck Johannes, Fischer Gunter, Schutkowski Mike
Max Planck Research Unit for Enzymology of Protein Folding, Halle, Germany.
Methods Mol Biol. 2010;669:173-81. doi: 10.1007/978-1-60761-845-4_14.
Protein function is highly regulated in pathways that are responsible for complex biochemical mechanisms such as growth, metabolism, and signal transduction. One of the most important mechanisms is posttranslational modification (PTM) changing protein surfaces by phosphorylation, sulfation, acetylation, methylation, glycosylation, and sumoylation resulting in a more than 100-fold higher complexity (Geiss-Friedlander and Melchior, Nat Rev Mol Cell Biol 8, 947-956, 2007; Hunter, Mol Cell 28, 730-738, 2007). This chapter presents a very efficient way to detect potential phosphorylation sites in protein families using overlapping peptides covering the complete primary structures (peptide scans) immobilized on glass slides. Results of kinase activity fingerprinting of cell lysates using peptide microarrays displaying peptide scans through all human peptidyl-prolyl-cis/trans-isomerases are shown.
蛋白质功能在负责复杂生化机制(如生长、代谢和信号转导)的途径中受到高度调控。最重要的机制之一是翻译后修饰(PTM),通过磷酸化、硫酸化、乙酰化、甲基化、糖基化和类泛素化改变蛋白质表面,导致其复杂性增加100多倍(盖斯-弗里德兰德和梅尔基奥尔,《自然综述:分子细胞生物学》8卷,947 - 956页,2007年;亨特,《分子细胞》28卷,730 - 738页,2007年)。本章介绍了一种非常有效的方法,利用覆盖完整一级结构的重叠肽段(肽扫描)固定在载玻片上,来检测蛋白质家族中潜在的磷酸化位点。展示了使用肽微阵列对细胞裂解物进行激酶活性指纹分析的结果,该肽微阵列展示了通过所有人类肽基脯氨酰顺/反异构酶的肽扫描。