Heltweg Birgit, Trapp Johannes, Jung Manfred
Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.
Methods. 2005 Aug;36(4):332-7. doi: 10.1016/j.ymeth.2005.03.003.
Histone deacetylases are important regulators of transcription and an emerging target for anticancer drugs. We present an overview over various assay formats that include radiolabelled histones, oligopeptides, and small molecules as substrates. The advantages and disadvantages of the various formats in terms of, e.g., substrate availability, throughput or subtype selectivity are discussed. Detailed procedures for various assay types that can be used for different problems, such as library screening or fluorescent inhibitor testing, are given. We present a new protocol for a simple high-throughput assay for NAD+-dependent (class III) histone deacetylases, also termed sirtuins.
组蛋白脱乙酰酶是转录的重要调节因子,也是抗癌药物的一个新兴靶点。我们概述了各种检测形式,包括以放射性标记的组蛋白、寡肽和小分子作为底物。讨论了各种形式在底物可用性、通量或亚型选择性等方面的优缺点。给出了可用于不同问题(如文库筛选或荧光抑制剂测试)的各种检测类型的详细程序。我们提出了一种用于NAD+依赖性(III类)组蛋白脱乙酰酶(也称为沉默调节蛋白)的简单高通量检测的新方案。