相关实验视频
Updated: Jul 16, 2025

09:11
Assays for Validating Histone Acetyltransferase Inhibitors
Published on: August 6, 2020
6.6K
药物化学在准I类组素脱乙酶方面取得了进展
Diaaeldin I Abdallah1,2, Elvin D de Araujo1, Naman H Patel1
1Department of Chemical & Physical Sciences, University of Toronto Mississauga, Mississauga, Ontario L5L 1C6, Canada.
Exploration of targeted anti-tumor therapy
|September 15, 2023
概括
基因脱乙酶 (HDACs) 调节基因表达,并与癌症等疾病有关. 本综述侧重于开发HDAC抑制剂 (HDACis),特别是I类HDAC,检查药物化学和药理学.
科学领域:
- 生物化学 生物化学
- 表观遗传学 在表观遗传学中,表观遗传学是指表观遗传学.
- 药理学 药理学是指药理学的学科.
背景情况:
- 基因脱乙酶 (HDACs) 是依赖的酶,对基因表达的表观遗传调节至关重要.
- HDACs控制蛋白质的乙化/脱乙化,影响DNA卷积和基因活性.
- HDACs的失调与癌症,神经退行性疾病,艾滋病毒和炎症性疾病有关.
研究的目的:
- 审查针对HDAC抑制剂 (HDACis) 的药物开发工作.
- 专注于第一类HDAC抑制剂.
- 检查HDACis的药用化学,结构设计和药理学.
主要方法:
- 对HDAC抑制剂研究的文献综述.
- 对药物化学方法的分析.
- 对结构设计原则的评估.
- 对HDAC抑制剂的药理学评估.
主要成果:
- 由于它们在疾病中的作用,HDACs是经过验证的治疗点.
- 在开发HDAC抑制剂方面取得了重大进展.
- 第I类HDAC是抑制剂开发的关键焦点.
- 药物化学和结构生物学指导了抑制剂的设计.
结论:
- 在各种疾病中,HDAC 抑制剂是一个有前途的治疗策略.
- 在药物化学和药理学方面的持续研究对于优化HDACis.是必不可少的.
- 针对I类HDACs提供了一种可行的药物开发方法.
相关概念视频
Spreading of Chromatin Modifications
8.3K
The histone proteins in the nucleosomes are post-translationally modified (PTM) to increase or decrease access to DNA. The commonly observed PTMs are methylation, acetylation, phosphorylation, and ubiquitination of lysine amino acids in the histone H3 tail region. These histone modifications have specific meaning for the cell. Hence, they are called "histone code". The protein complex involved in histone modification is termed as "reader-writer" complex.
Writers
The writer...
Writers
The writer...
8.3K
Histone Modification
13.4K
The histone proteins have a flexible N-terminal tail extending out from the nucleosome. These histone tails are often subjected to post-translational modifications such as acetylation, methylation, phosphorylation, and ubiquitination. Particular combinations of these modifications form “histone codes” that influence the chromatin folding and tissue-specific gene expression.
Acetylation
The enzyme histone acetyltransferase adds acetyl group to the histones. Another enzyme, histone...
Acetylation
The enzyme histone acetyltransferase adds acetyl group to the histones. Another enzyme, histone...
13.4K
Histone Variants at the Centromere
4.4K
Histone variants are the histone proteins with structural and sequence variations. These variants may be regarded as “mutant” forms that replace their canonical histone counterparts in the nucleosomes. Specific post-translational modifications on the histone variants enable further chromatin complexity and regulate tissue-specific gene expression. The most common histone variants are from histone H2A, H2B, and linker histone H1 families. However, several variants of histone H3...
4.4K
Chromatin Modification in iPS Cells
1.7K
Chromatin modification alters gene expression; therefore, scientists can add histone-modifying enzymes, histone variants, and chromatin remodeling complexes to somatic cells to aid reprogramming into pluripotent stem (iPS) cells.
Compact chromatin makes reprogramming difficult. Enzymes, such as histone demethylases and acetyltransferases, are often added during reprogramming to loosen the chromatin, making the DNA more accessible to transcription factors. Molecules that inhibit histone...
Compact chromatin makes reprogramming difficult. Enzymes, such as histone demethylases and acetyltransferases, are often added during reprogramming to loosen the chromatin, making the DNA more accessible to transcription factors. Molecules that inhibit histone...
1.7K
Acid Suppressive Drugs for Peptic Ulcer Disease: Histamine H2-Receptor Antagonists
511
Histamine H2 receptors, which are intricately located on the basolateral membrane of parietal cells, play a crucial role in modulating gastric acid secretion. When released from enterochromaffin-like cells, histamine engages H2 receptors, initiating the cyclic AMP (cAMP) pathway. In this pathway, adenylyl cyclase converts ATP into cAMP, elevating intracellular cAMP levels. The activation of protein kinase A follows, stimulating the proton pump. This stimulation prompts the secretion of hydrogen...
511

