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四种主要不同类型的人类磷脂酶A综述。

Review of four major distinct types of human phospholipase A.

作者信息

Vasquez Alexis M, Mouchlis Varnavas D, Dennis Edward A

机构信息

Department of Chemistry and Biochemistry and Department of Pharmacology, School of Medicine, University of California, San Diego, La Jolla, CA 92093-0601, United States.

Department of Chemistry and Biochemistry and Department of Pharmacology, School of Medicine, University of California, San Diego, La Jolla, CA 92093-0601, United States.

出版信息

Adv Biol Regul. 2018 Jan;67:212-218. doi: 10.1016/j.jbior.2017.10.009. Epub 2017 Oct 23.

Abstract

The phospholipase A superfamily of enzymes plays a significant role in the development and progression of numerous inflammatory diseases. Through their catalytic action on membrane phospholipids, phospholipases are the upstream regulators of the eicosanoid pathway releasing free fatty acids for cyclooxygenases, lipoxygenases, and cytochrome P450 enzymes which produce various well-known inflammatory mediators including leukotrienes, thromboxanes and prostaglandins. Elucidating the association of phospholipases A with the membrane, the extraction and binding of phospholipid substrates, and their interactions with small-molecule inhibitors is crucial for the development of new anti-inflammatory therapeutics. Studying phospholipases has been challenging because they act on the surface of cellular membranes and micelles. Multidisciplinary approaches including hydrogen/deuterium exchange mass spectrometry, molecular dynamics simulations, and other computer-aided drug design techniques have been successfully employed by our laboratory to study interactions of phospholipases with membranes, phospholipid substrates and inhibitors. This review summarizes the application of these techniques to study four human recombinant phospholipases A.

摘要

磷脂酶A超家族的酶在众多炎症性疾病的发生和发展中起着重要作用。通过对膜磷脂的催化作用,磷脂酶是类花生酸途径的上游调节因子,可释放游离脂肪酸供环氧化酶、脂氧合酶和细胞色素P450酶使用,这些酶可产生包括白三烯、血栓素和前列腺素在内的各种著名的炎症介质。阐明磷脂酶A与膜的关联、磷脂底物的提取和结合以及它们与小分子抑制剂的相互作用对于开发新的抗炎疗法至关重要。研究磷脂酶具有挑战性,因为它们作用于细胞膜和微团的表面。我们实验室成功采用了包括氢/氘交换质谱、分子动力学模拟和其他计算机辅助药物设计技术在内的多学科方法来研究磷脂酶与膜、磷脂底物和抑制剂的相互作用。本综述总结了这些技术在研究四种人重组磷脂酶A中的应用。

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