Department of Biological Sciences, East Tennessee State University, Johnson City, 37614, USA.
Curr Med Chem. 2010;17(25):2822-36. doi: 10.2174/092986710791859270.
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.
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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