Kortesuo P T, Nevalainen T J
Department of Pathology, University of Turku, Finland.
Biochem J. 1991 Aug 15;278 ( Pt 1)(Pt 1):263-7. doi: 10.1042/bj2780263.
A phospholipase A2 (PLA2, EC 3.1.1.4) was purified from human cell-free ascitic fluid (a-PLA2) by ion-exchange chromatography and h.p.l.c. on a reverse-phase column to apparent homogeneity. The enzyme had an Mr of approx. 10,000 as determined by SDS/PAGE. Polyclonal antibodies raised in a rabbit were specific to a-PLA2, as judged by immunoblotting. A time-resolved fluoroimmunoassay (TR-FIA) for measuring the concentration of a-PLA2 in various body fluids was developed. The detection limit of the assay was about 6 ng/ml. The antiserum did not cross-react with pancreatic secretory phospholipase A2 as measured by TR-FIA. The enzyme content was studied in various samples, including normal human serum, buffy-coat leucocytes, synovial fluid, and pancreas and spleen homogenates.
通过离子交换色谱法和反相柱高效液相色谱法从人无细胞腹水(a-PLA2)中纯化出一种磷脂酶A2(PLA2,EC 3.1.1.4),达到表观均一性。通过SDS/PAGE测定,该酶的Mr约为10,000。通过免疫印迹判断,在兔体内产生的多克隆抗体对a-PLA2具有特异性。开发了一种时间分辨荧光免疫分析法(TR-FIA)用于测量各种体液中a-PLA2的浓度。该分析方法的检测限约为6 ng/ml。通过TR-FIA测量,抗血清与胰腺分泌性磷脂酶A2无交叉反应。对包括正常人血清、血沉棕黄层白细胞、滑液以及胰腺和脾脏匀浆在内的各种样品中的酶含量进行了研究。