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来自蚊虫寄生虫巨大拉格孢菌的磷脂酶A2的固醇和固醇酯调节

Sterol and steryl ester regulation of phospholipase A2 from the mosquito parasite Lagenidium giganteum.

作者信息

Kerwin J L, MacKichan J K, Semon M J, Wiens A M, DeRose C C, Torvik J J

机构信息

Botany Department 351330, University of Washington, Seattle 98195-1330, USA.

出版信息

Lipids. 1996 Nov;31(11):1179-88. doi: 10.1007/BF02524293.

Abstract

Lagenidium giganteum, a facultative parasite of mosquito larvae, cannot synthesize sterols, and requires an exogenous source of these lipids in order to enter its reproductive cycle. This parasite grows vegetatively in the absence of sterols, but requires cholesterol or structurally related compounds to produce motile zoospores, which are the only stage capable of infecting mosquitoes. Sterols structurally related to cholesterol and some steryl esters inhibited the activity of L. giganteum phospholipase A2 (PLA2), an enzyme that hydrolyzes fatty acids from the sn-2 position of glycerophospholipids. Sterols that induce reproduction inhibited L. giganteum PLA2 activity, while sterols and steroids that do not support sporulation had minimal effect. Most steryl esters had no effect on enzyme activity, but cholesteryl arachidonate (CA) was a potent inhibitor of parasite PLA2. Not all enzymes partly purified using a DEAE-Sephacel column were affected by these lipids, demonstrating selective inhibition of specific enzymes. Potency was enhanced by up to several orders of magnitude if epoxy fatty acids were esterified to the cholesterol nucleus. The steryl ester pool was dynamic during morphogenesis, and the fatty acid composition of the steryl esters did not mimic total cell or membrane (glycerophospholipid) fatty acid composition as L. giganteum proceeded through its growth cycle. Synthesis of CA and monoepoxy CA by the parasite was confirmed using electrospray mass spectrometry and collision-induced dissociation. Steryl derivatives selectively inhibited PLA2 enzymes from bovine pancreas, snake venom, and human cytoplasmic 85-kDa PLA2.

摘要

巨大拉格孢菌是蚊子幼虫的兼性寄生虫,无法合成甾醇,需要外源脂质才能进入其繁殖周期。这种寄生虫在没有甾醇的情况下进行营养生长,但需要胆固醇或结构相关化合物来产生游动孢子,游动孢子是唯一能够感染蚊子的阶段。与胆固醇结构相关的甾醇和一些甾醇酯抑制了巨大拉格孢菌磷脂酶A2(PLA2)的活性,PLA2是一种从甘油磷脂的sn-2位水解脂肪酸的酶。诱导繁殖的甾醇抑制了巨大拉格孢菌PLA2的活性,而不支持孢子形成的甾醇和类固醇的影响最小。大多数甾醇酯对酶活性没有影响,但花生四烯酸胆固醇酯(CA)是寄生虫PLA2的有效抑制剂。并非所有使用DEAE-葡聚糖凝胶柱部分纯化的酶都受到这些脂质的影响,但证明了对特定酶的选择性抑制。如果环氧脂肪酸酯化到胆固醇核上,效力可提高几个数量级。在形态发生过程中,甾醇酯库是动态的,随着巨大拉格孢菌经历其生长周期,甾醇酯的脂肪酸组成并不模仿总细胞或膜(甘油磷脂)脂肪酸组成。利用电喷雾质谱和碰撞诱导解离证实了寄生虫对CA和单环氧CA的合成。甾醇衍生物选择性地抑制来自牛胰腺、蛇毒和人细胞质85-kDa PLA2的PLA2酶。

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