串扰
蛋白质组
蛋白质组学
计算生物学
翻译后修饰
计算机科学
化学
生物
生物信息学
生物化学
电子工程
工程类
基因
酶
作者
Mario Leutert,Samuel Entwisle,Judit Villén
标识
DOI:10.1016/j.mcpro.2021.100129
摘要
Post-translational modification (PTM) of proteins allows cells to regulate protein functions, transduce signals and respond to perturbations. PTMs expand protein functionality and diversity, which leads to increased proteome complexity. PTM crosstalk describes the combinatorial action of multiple PTMs on the same or on different proteins for higher order regulation. Here we review how recent advances in proteomic technologies, mass spectrometry instrumentation, and bioinformatics spurred the proteome-wide identification of PTM crosstalk through measurements of PTM sites. We provide an overview of the basic modes of PTM crosstalk, the proteomic methods to elucidate PTM crosstalk, and approaches that can inform about the functional consequences of PTM crosstalk.
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