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用于探测组蛋白去乙酰化酶(HDAC)活性的化学工具。

Chemical tools for probing histone deacetylase (HDAC) activity.

作者信息

Minoshima Masafumi, Kikuchi Kazuya

机构信息

Graduate School of Engineering, 2) Institute of Academic Initiatives, Osaka University 2-1 Yamadaoka, Suita, Osaka 565-0871, Japan..

出版信息

Anal Sci. 2015;31(4):287-92. doi: 10.2116/analsci.31.287.

Abstract

Histone deacetylases (HDACs) enzymes are responsible for removing epigenetic markers on histone proteins, which results in chromatin inactivation and gene repression. An evaluation of HDAC activity is essential for not only determining the physiological function of HDACs, but also for developing HDAC-targeting drugs. This review focuses on the chemical tools used to detect HDAC activity. We highlight activity-based probes and positron emission tomography probes based on the chemical structure of the inhibitors. We also summarize fluorogenic probes used in single-step methods for HDAC detection. These fluorogenic probes are designed based on the nucleophilicity of the amino group, aggregation via electrostatic interactions, and changes in the DNA binding properties. These fluorogenic systems may enable facile and rapid screening to evaluate HDAC inhibitors, which will contribute to the development of epigenetic drugs.

摘要

组蛋白去乙酰化酶(HDACs)负责去除组蛋白上的表观遗传标记,从而导致染色质失活和基因抑制。评估HDAC活性不仅对于确定HDAC的生理功能至关重要,而且对于开发靶向HDAC的药物也至关重要。本综述重点关注用于检测HDAC活性的化学工具。我们强调基于抑制剂化学结构的基于活性的探针和正电子发射断层扫描探针。我们还总结了用于HDAC单步检测方法的荧光探针。这些荧光探针是基于氨基的亲核性、通过静电相互作用的聚集以及DNA结合特性的变化而设计的。这些荧光系统可以实现简便快速的筛选以评估HDAC抑制剂,这将有助于表观遗传药物的开发。

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