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Chemical Biology Approaches for Investigating the Functions of Lysine Acetyltransferases

机译:用于研究赖氨酸乙酰转移酶功能的化学生物学方法

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摘要

The side-chain acetylation of lysine residues in histones and non-histone proteins catalyzed by lysine acetyltransferases (KATs) represents a widespread posttranslational modification (PTM) in the eukaryotic cells. Lysine acetylation plays regulatory roles in major cellular pathways inside and outside the nucleus. In particular, KAT-mediated histone acetylation has an effect on all DNA-templated epigenetic processes. Aberrant expression and activation of KATs are commonly observed in human diseases, especially cancer. In recent years, the study of KAT functions in biology and disease has greatly benefited from chemical biology tools and strategies. In this Review, we present the past and current accomplishments in the design of chemical biology approaches for the interrogation of KAT activity and function. These methods and probes are classified according to their mechanisms of action and respective applications, with both strengths and limitations discussed.
机译:由赖氨酸乙酰转移酶(KATS)催化的组蛋白和非组蛋白蛋白中赖氨酸残基的侧链乙酰化代表了真核细胞中的广泛的后翻译改性(PTM)。 赖氨酸乙酰化在细胞核内外的主要细胞途径中起着调节作用。 特别地,KAT介导的组蛋白乙酰化对所有DNA模板化的表观遗传过程具有效果。 在人类疾病,尤其是癌症中通常观察到异常的表达和kats的活化。 近年来,生物学和疾病中KAT功能的研究极大地受益于化学生物学工具和策略。 在本次审查中,我们介绍了过去的化学生物学方法的过去和目前的成就,用于审查KAT活性和功能。 这些方法和探针根据其行动机制和各自的应用程序进行分类,讨论了强度和局限性。

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