Gelb M H, Jain M K, Berg O G
Department of Chemistry, University of Washington, Seattle 98195.
FASEB J. 1994 Sep;8(12):916-24. doi: 10.1096/fasebj.8.12.8088457.
Phospholipases A2 are involved in inflammatory processes such as the liberation of free arachidonic acid from the membrane pool for the biosynthesis of eicosanoids. Inhibitors of these enzymes are proving useful in determining the biological roles of phospholipases A2 in complex cellular processes and may also have therapeutic potential. Inhibition of these lipolytic enzymes is more difficult to characterize as the enzymatic reaction occurs at a lipid/water interface. This review focuses on the description of a number of classes of rationally designed phospholipase A2 inhibitors. The development of a theoretical framework for the proper analysis of inhibitors is presented. Structural studies of phospholipase A2-inhibitor complexes suggest how the lipolysis reaction is catalyzed. Finally, some recent results on the use of phospholipase A2 inhibitors in living cells and tissues are revealed.
磷脂酶A2参与炎症过程,如从膜池中释放游离花生四烯酸用于类二十烷酸的生物合成。事实证明,这些酶的抑制剂在确定磷脂酶A2在复杂细胞过程中的生物学作用方面很有用,并且可能还具有治疗潜力。由于酶促反应发生在脂质/水界面,因此对这些脂解酶的抑制作用更难表征。本综述重点描述了几类合理设计的磷脂酶A2抑制剂。提出了用于正确分析抑制剂的理论框架的发展。磷脂酶A2-抑制剂复合物的结构研究表明了脂解反应是如何被催化的。最后,揭示了一些关于在活细胞和组织中使用磷脂酶A2抑制剂的最新结果。