Reynolds L J, Hughes L L, Yu L, Dennis E A
Department of Chemistry, University of California at San Diego, La Jolla 92093-0601.
Anal Biochem. 1994 Feb 15;217(1):25-32. doi: 10.1006/abio.1994.1079.
Human cytosolic phospholipase A2 (cPLA2) is an 85-kDa protein which displays a preference for arachidonoyl phospholipids as substrates. This substrate preference and the assay characteristics of the enzyme are quite different from those of the smaller, more well-studied extracellular PLA2s. We now report the development of a nonradioactive, spectrophotometric, microtiterplate assay for human cPLA2 using a novel synthetic thio-phospholipid analog as a substrate. This substrate is a phosphatidylcholine derivative with an arachidonoylthioester in the sn-2 position and an alkyl-ether in the sn-1 position. The use of an sn-1 alkyl-ether in the substrate ensures that the assay will only measure PLA2 activity and will not be complicated by the metabolism of the lysophospholipid product by the enzyme's lysophospholipase activity. cPLA2 is assayed at pH 7.4 and 37 degrees C with a mixed micellar substrate consisting of 2 mM thio-phospholipid and 4 mM Triton X-100 in 30% glycerol. Under these conditions, the assay is fairly linear for over 1 h.
人胞质磷脂酶A2(cPLA2)是一种85 kDa的蛋白质,它对花生四烯酰磷脂表现出底物偏好性。这种底物偏好性以及该酶的检测特性与较小的、研究更为充分的细胞外磷脂酶A2有很大不同。我们现在报告一种用于人cPLA2的非放射性分光光度法微孔板检测方法的开发,该方法使用一种新型合成硫代磷脂类似物作为底物。这种底物是一种磷脂酰胆碱衍生物,在sn-2位有花生四烯酰硫酯,在sn-1位有烷基醚。底物中使用sn-1烷基醚可确保该检测仅测量磷脂酶A2活性,且不会因该酶的溶血磷脂酶活性对溶血磷脂产物的代谢而变得复杂。在pH 7.4和37℃条件下,使用由2 mM硫代磷脂和4 mM Triton X-100在30%甘油中组成的混合胶束底物来检测cPLA2。在这些条件下,该检测在1小时以上相当线性。