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芋螺地平-M,一种从海蜗牛芋螺毒液中分离出的新型磷脂酶A2。

Conodipine-M, a novel phospholipase A2 isolated from the venom of the marine snail Conus magus.

作者信息

McIntosh J M, Ghomashchi F, Gelb M H, Dooley D J, Stoehr S J, Giordani A B, Naisbitt S R, Olivera B M

机构信息

Department of Psychiatry, University of Utah, Salt Lake City 84112.

出版信息

J Biol Chem. 1995 Feb 24;270(8):3518-26. doi: 10.1074/jbc.270.8.3518.

Abstract

We describe the purification and first biochemical characterization of an enzymatic activity in venom from the marine snail Conus magus. This enzyme, named conodipine-M, is a novel phospholipase A2 with a molecular mass of 13.6 kDa and is comprised of two polypeptide chains linked by one or more disulfide bonds. The amino acid sequence of conodipine-M shows little if any homology to other previously sequenced phospholipase A2 enzymes (PLA2s). Conodipine-M thus represents a new group of PLA2s. This is remarkable, since conodipine-M displays a number of properties that are similar to those of previously characterized 14-kDa PLA2s. The enzyme shows little, if any, phospholipase A1, diacyglycerol lipase, triacylglycerol lipase, or lysophospholipase activities. Conodipine-M hydrolyzes the sn-2 ester of various preparations of phospholipid only in the presence of calcium and with specific activities that are comparable to those of well known 14-kDa snake venom and pancreatic PLA2s. The Conus enzyme binds tightly to vesicles of the negatively charged phospholipid 1,2-dimyristoyl-sn-glycero-3-phosphomethanol and catalyzes the hydrolysis of this substrate in a processive fashion. Conodipine-M does not significantly discriminate against phospholipids with unsaturated versus saturated fatty acids at the sn-2 position or with different polar head groups. Linoleoyl amide and a phospholipid analog containing an alkylphosphono group at the sn-2 position are potent inhibitors of conodipine-M. We suggest that the functional resemblance of conodipine-M to other PLA2s might be explained by the utilization of similar catalytic residues.

摘要

我们描述了从海洋蜗牛芋螺毒液中一种酶活性的纯化及首次生化特性分析。这种酶名为芋螺地平 - M,是一种新型磷脂酶A2,分子量为13.6 kDa,由一条或多条二硫键连接的两条多肽链组成。芋螺地平 - M的氨基酸序列与其他先前测序的磷脂酶A2(PLA2s)几乎没有同源性。因此,芋螺地平 - M代表了一类新的PLA2s。这很显著,因为芋螺地平 - M表现出许多与先前表征的14 kDa PLA2s相似的特性。该酶几乎没有磷脂酶A1、甘油二酯脂肪酶、甘油三酯脂肪酶或溶血磷脂酶活性。芋螺地平 - M仅在钙离子存在的情况下,以与著名的14 kDa蛇毒和胰腺PLA2s相当的比活性水解各种磷脂制剂的sn - 2酯。芋螺酶与带负电荷的磷脂1,2 - 二肉豆蔻酰 - sn - 甘油 - 3 - 磷酸甲醇的囊泡紧密结合,并以连续方式催化该底物的水解。芋螺地平 - M对sn - 2位具有不饱和脂肪酸与饱和脂肪酸或不同极性头部基团的磷脂没有明显的区分。亚油酰胺和在sn - 2位含有烷基膦酸基团的磷脂类似物是芋螺地平 - M的有效抑制剂。我们认为,芋螺地平 - M与其他PLA2s的功能相似性可能是由于利用了相似的催化残基来解释。

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