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ATP 合酶的药物化学:膳食多酚和两栖动物抗菌肽的潜在药物靶点。

Medicinal chemistry of ATP synthase: a potential drug target of dietary polyphenols and amphibian antimicrobial peptides.

机构信息

Department of Biological Sciences, East Tennessee State University, Johnson City, 37614, USA.

出版信息

Curr Med Chem. 2010;17(25):2822-36. doi: 10.2174/092986710791859270.


DOI:10.2174/092986710791859270
PMID:20586714
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4734657/
Abstract

In this review we discuss the inhibitory effects of dietary polyphenols and amphibian antimicrobial/antitumor peptides on ATP synthase. In the beginning general structural features highlighting catalytic and motor functions of ATP synthase will be described. Some details on the presence of ATP synthase on the surface of several animal cell types, where it is associated with multiple cellular processes making it an interesting drug target with respect to dietary polyphenols and amphibian antimicrobial peptides will also be reviewed. ATP synthase is known to have distinct polyphenol and peptide binding sites at the interface of α/β subunits. Molecular interaction of polyphenols and peptides with ATP synthase at their respective binding sites will be discussed. Binding and inhibition of other proteins or enzymes will also be covered so as to understand the therapeutic roles of both types of molecules. Lastly, the effects of polyphenols and peptides on the inhibition of Escherichia coli cell growth through their action on ATP synthase will also be presented.

摘要

在这篇综述中,我们讨论了膳食多酚和两栖动物抗菌/抗肿瘤肽对 ATP 合酶的抑制作用。首先,我们将描述 ATP 合酶的一般结构特征,突出其催化和马达功能。我们还将回顾一些关于几种动物细胞类型表面存在 ATP 合酶的细节,在这些细胞中,它与多种细胞过程相关联,使其成为一个有趣的药物靶点,涉及膳食多酚和两栖动物抗菌肽。已知 ATP 合酶在 α/β 亚基的界面上具有独特的多酚和肽结合位点。我们将讨论多酚和肽与 ATP 合酶在各自结合位点的分子相互作用。还将涵盖与其他蛋白质或酶的结合和抑制,以了解这两种类型分子的治疗作用。最后,我们还将介绍多酚和肽通过作用于 ATP 合酶对大肠杆菌细胞生长的抑制作用。

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本文引用的文献

[1]
Dietary bioflavonoids inhibit Escherichia coli ATP synthase in a differential manner.

Int J Biol Macromol. 2010-3-25

[2]
Concentration-dependent effect of (-) epicatechin in hypertensive patients.

Phytother Res. 2010-10

[3]
Inhibition of Escherichia coli ATP synthase by amphibian antimicrobial peptides.

Int J Biol Macromol. 2010-1-25

[4]
Novel Inhibitors of Fatty Acid Synthase with Anticancer Activity.

Clin Cancer Res. 2009-12-15

[5]
Multiple molecular targets of resveratrol: Anti-carcinogenic mechanisms.

Arch Biochem Biophys. 2009-6-15

[6]
Temporins and their synergism against Gram-negative bacteria and in lipopolysaccharide detoxification.

Biochim Biophys Acta. 2009-8

[7]
Inhibition of ATPase activity of Escherichia coli ATP synthase by polyphenols.

Int J Biol Macromol. 2009-7-1

[8]
Role of {alpha}-subunit VISIT-DG sequence residues Ser-347 and Gly-351 in the catalytic sites of Escherichia coli ATP synthase.

J Biol Chem. 2009-4-17

[9]
Identification and characterisation of a novel antimicrobial polypeptide from the skin secretion of a Chinese frog (Rana chensinensis).

Int J Antimicrob Agents. 2009-6

[10]
Hylin a1, the first cytolytic peptide isolated from the arboreal South American frog Hypsiboas albopunctatus ("spotted treefrog").

Peptides. 2009-2

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