基于肽的表观遗传蛋白抑制剂。

3区 生物学 Q2 Biochemistry, Genetics and Molecular Biology
Jordi C J Hintzen, Jasmin Mecinović
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引用次数: 0

摘要

在过去二十年里,表观遗传药物发现已成为药物化学不可或缺的一部分。靶向表观遗传蛋白--修饰组蛋白和 DNA 的酶类(书写者和擦除者)以及识别此类修饰的蛋白(阅读者)--已被确定为治疗包括癌症和神经系统疾病在内的多种人类疾病的药物策略。在本章中,我们将系统介绍基于肽的表观遗传蛋白抑制剂,这些抑制剂在结构和功能上具有多样性。我们的研究表明,DNA 甲基转移酶、组蛋白甲基转移酶和组蛋白乙酰转移酶等表观遗传作者可以被具有非蛋白源氨基酸的多肽有效抑制。此外,包括 TET 酶、组蛋白去甲基化酶和组蛋白去乙酰化酶在内的表观遗传清除剂的活性可被多种线性和环状肽选择性地调节。此外,我们还讨论了可被组蛋白模拟肽抑制的染色质结合表观遗传阅读蛋白。总之,本章强调肽为学术界和工业界的表观遗传药物发现计划提供了一个重要的分子平台。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Peptide-based inhibitors of epigenetic proteins.

Epigenetic drug discovery has become an integral part of medicinal chemistry in the past two decades. Targeting epigenetic proteins-enzymes that modify histone proteins and DNA (writers and erasers) and proteins that recognize such modifications (readers)-has been firmly established as a medicinal strategy for treatment of many human diseases, including cancer and neurological disorders. In this chapter, we systematically describe peptide-based inhibitors of structurally and functionally diverse classes of epigenetic proteins. We show that epigenetic writers, such as DNA methyltransferases, histone methyltransferases and histone acetyltransferases, can be efficiently inhibited by peptides possessing nonproteinogenic amino acids. Moreover, the activity of epigenetic erasers, including TET enzymes, histone demethylases, and histone deacetylases, can be selectively modulated by diverse linear and cyclic peptides. Furthermore, we discuss chromatin-binding epigenetic reader proteins that can be inhibited by histone-mimicking peptides. Overall, this chapter highlights that peptides provide an important molecular platform for epigenetic drug discovery programmes in academia and industry.

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来源期刊
CiteScore
6.90
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: Progress in Molecular Biology and Translational Science (PMBTS) provides in-depth reviews on topics of exceptional scientific importance. If today you read an Article or Letter in Nature or a Research Article or Report in Science reporting findings of exceptional importance, you likely will find comprehensive coverage of that research area in a future PMBTS volume.
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