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小鼠淋巴细胞的磷脂酰肌醇特异性磷脂酶C

Phosphatidylinositol-specific phospholipase C of murine lymphocytes.

作者信息

Kamisaka Y, Toyoshima S, Osawa T

出版信息

Arch Biochem Biophys. 1986 Sep;249(2):569-78. doi: 10.1016/0003-9861(86)90035-4.

Abstract

Phosphatidylinositol-specific phospholipase C (PI-phospholipase C) was found primarily in the cytosolic fraction of murine splenic lymphocytes. However, small but significant amounts of the activity of the enzyme were detected in the microsome and plasma membrane fractions. Both the cytosolic and membrane-bound phospholipases C specifically hydrolyzed inositol phospholipids, phosphatidylinositol, phosphatidylinositol 4-phosphate, and phosphatidylinositol 4,5-bisphosphate. PI-Phospholipase C activity was detected in the cytosolic and microsome fractions from both T-cell-enriched and B-cell-enriched spleen cells. The membrane-bound enzyme was distinguishable from the cytosolic enzyme in the following properties. The cytosolic PI-phospholipase C showed optimal activity at pH 6.0 while the membrane-bound enzyme had two pH optima between pH 5.0 and 7.0. The activity of the cytosolic enzyme was first detected at 1 microM Ca2+, and maximum activity was observed at 100 microM Ca2+, while the membrane-bound PI-phospholipase C required higher Ca2+ concentrations, of millimolar order. The membrane-bound enzyme could hardly be extracted with 1 M NaCl but was extracted with 0.4% cholate.A portion of the membrane-bound PI-phospholipase C activity in the cholate extract was absorbed by concanavalin A-Sepharose and specifically eluted with an alpha-methylmannoside solution. The cytosolic enzyme, which was water soluble, did not bind to concanavalin A-Sepharose. Trypsinization of lymphocytes before subcellular fractionation caused a significant decrease in the PI-phospholipase C activity in the microsome fraction but almost no loss at all of the cytosolic enzyme activity.

摘要

磷脂酰肌醇特异性磷脂酶C(PI-磷脂酶C)主要存在于小鼠脾淋巴细胞的胞质部分。然而,在微粒体和质膜部分也检测到了少量但显著的该酶活性。胞质和膜结合的磷脂酶C都能特异性水解肌醇磷脂、磷脂酰肌醇、磷脂酰肌醇4-磷酸和磷脂酰肌醇4,5-二磷酸。在富含T细胞和富含B细胞的脾细胞的胞质和微粒体部分均检测到了PI-磷脂酶C活性。膜结合酶与胞质酶在以下特性上有所不同。胞质PI-磷脂酶C在pH 6.0时表现出最佳活性,而膜结合酶在pH 5.0至7.0之间有两个最佳pH值。胞质酶的活性在1微摩尔Ca2+时首次被检测到,在100微摩尔Ca2+时观察到最大活性,而膜结合的PI-磷脂酶C需要更高浓度的Ca2+,达到毫摩尔级别。膜结合酶几乎不能用1 M NaCl提取,但能用0.4%胆酸盐提取。胆酸盐提取物中一部分膜结合的PI-磷脂酶C活性被伴刀豆球蛋白A-琼脂糖吸附,并用α-甲基甘露糖苷溶液特异性洗脱。水溶性的胞质酶不与伴刀豆球蛋白A-琼脂糖结合。在亚细胞分级分离前用胰蛋白酶处理淋巴细胞会导致微粒体部分的PI-磷脂酶C活性显著降低,但胞质酶活性几乎没有损失。

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