Epigenetic Histone Deacetylases Activity Assay in the Brain and Peripheral Organ Tissues

IF 2.2
Doodipala Samba Reddy, Hudson Boyd, Vinitha Karnati, Joon Kim, Sreevidhya Ramakrishnan, Xin Wu
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Abstract

Histone deacetylases (HDACs) are crucial epigenetic regulators involved in the modulation of gene expression and are promising therapeutic targets for treating various diseases, including central nervous system disorders and cancer. HDAC inhibitors exhibit neuroprotective, antiepileptogenic, and antidepressant properties in animal models, underscoring their clinical relevance. Quantifying HDAC activity is essential for identifying inhibitors and evaluating their effects under physiological or pathological conditions. This article outlines a comprehensive, sensitive, and robust assay to quantify HDAC activity in tissue lysates, with specific application to brain tissue. The assay is based on the catalytic removal of an acetyl group from the Boc-Lys(Ac)-AMC substrate by HDAC enzymes. Following nuclear protein extraction, tissue HDAC activity can be quantitatively assessed using a fluorometric Boc-Lys(Ac) HDAC activity kit. Adding a developer containing trypsin then converts the deacetylated product into a measurable fluorophore. This enables precise quantification of HDAC activity levels across different tissues, making the method suitable for screening putative HDAC inhibitors and assessing their effects on epigenetically modulated phenotypes. We validated these protocols using brain tissue samples from mice subjected to traumatic brain injury, a condition known to elevate HDAC activity levels. This assay provides an efficient, scalable tool for exploring HDAC function, evaluating therapeutic interventions, and advancing the understanding of HDAC-mediated mechanisms in animal models. © 2025 The Author(s). Current Protocols published by Wiley Periodicals LLC.

Basic Protocol 1: Isolation of nuclear protein from brain and other tissues

Support Protocol 1: Harvesting and microdissection of brain and other tissues

Support Protocol 2: Estimation of extracted protein using the Pierce bicinchoninic acid (BCA) assay

Basic Protocol 2: HDAC activity fluorometric assay in the brain and other tissues

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脑及外周器官组织表观遗传组蛋白去乙酰化酶活性测定
组蛋白去乙酰化酶(hdac)是参与基因表达调节的重要表观遗传调控因子,是治疗包括中枢神经系统疾病和癌症在内的各种疾病的有希望的治疗靶点。在动物模型中,HDAC抑制剂表现出神经保护、抗癫痫和抗抑郁的特性,强调了它们的临床相关性。定量测定HDAC活性对于识别抑制剂和评估其在生理或病理条件下的作用至关重要。这篇文章概述了一个全面的,敏感的,和强大的测定来量化组织裂解物中的HDAC活性,具体应用于脑组织。该分析是基于HDAC酶催化去除Boc-Lys(Ac)-AMC底物中的乙酰基。核蛋白提取后,可以使用荧光Boc-Lys(Ac) HDAC活性试剂盒定量评估组织HDAC活性。然后加入含有胰蛋白酶的显影剂,将去乙酰化产物转化为可测量的荧光团。这可以精确量化不同组织中的HDAC活性水平,使该方法适用于筛选假定的HDAC抑制剂并评估其对表观遗传调节表型的影响。我们使用创伤性脑损伤小鼠的脑组织样本验证了这些方案,这种情况已知会提高HDAC活性水平。该试验为探索HDAC功能、评估治疗干预措施以及在动物模型中推进对HDAC介导机制的理解提供了一种高效、可扩展的工具。©2025作者。Wiley期刊有限责任公司发表的当前协议基本协议1:从脑和其他组织中分离核蛋白支持协议1:从脑和其他组织中收获和显微解剖支持协议2:使用Pierce bicinchoninic酸(BCA)测定法估计提取的蛋白质基本协议2:脑和其他组织中的HDAC活性荧光测定
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