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对磷酸肌醇具有特异性的核磷脂酶C的纯化与特性分析

Purification and characterization of nuclear phospholipase C specific for phosphoinositides.

作者信息

Asano M, Tamiya-Koizumi K, Homma Y, Takenawa T, Nimura Y, Kojima K, Yoshida S

机构信息

First Department of Surgery, Nagoya University School of Medicine, Japan.

出版信息

J Biol Chem. 1994 Apr 22;269(16):12360-6.

PMID:8163540
Abstract

A phosphoinositide-specific phospholipase C (PLC) was solubilized from the isolated nuclei of rat ascites hepatoma AH7974 cells by ultrasonication in 2 M KCl. The extract was then subjected to five steps of column chromatographies in the order of Sephacryl S-300, phosphocellulose, Mono Q, Mono S, and Superose 6. Four forms of PLC (tentatively designated as N1, N2, N3, and N4) were purified 440-1400-fold. N1, N2, N3, and N4 showed apparent molecular masses of 85, 83, 80, and 88 kDa, respectively, on SDS-polyacrylamide gel electrophoresis. N1 cross-reacted with the antibody against the delta 1 isoform, while the other three forms did not cross-react with any of the antibodies against PLC-delta 1, -gamma 1, -gamma 2, and -beta 1. They hydrolyzed phosphatidylinositol (PI), phosphatidylinositol 4-monophosphate (PIP), and phosphatidylinositol 4,5-bisphosphate (PIP2) but did not show any activities against phosphatidylcholine and phosphatidylethanolamine. They showed the same optimal pH:pH 6.5 for PI hydrolysis and pH 7.0 for both PIP and PIP2 hydrolyses. They absolutely required Ca2+ for activity, with optimal concentrations of 10(-3)-10(-5) M for PIP and 10(-4)-10(-5) M for PIP2. For PI hydrolysis, N1, N2, and N3 required a Ca2+ concentration higher than 10(-2) M whereas N4 revealed significant activity even at 10(-5) M Ca2+ concentrations. Two forms of plasma membrane PLC and three forms of cytosolic PLC were purified from AH7974 cells by the same procedure as for nuclear PLC. Comparative study with these three groups revealed that all of the purified PLC isoforms shared similar enzymological properties except N4, which showed an exceptionally high affinity to Mono S column and was active at low concentrations of Ca2+ for PI as substrate. Furthermore, when PLC isoforms of nuclei from adult resting rat liver were compared with those from regenerating rat liver after partial hepatectomy, a PLC isoform corresponding to N4 of AH7974 cells was found only in regenerating liver nuclei. From these results, it was suggested that the nuclei of growing liver cells possessed a unique form of PLC (N4).

摘要

通过在2M KCl中超声处理,从大鼠腹水肝癌AH7974细胞的分离核中溶解出一种磷酸肌醇特异性磷脂酶C(PLC)。然后将提取物依次通过Sephacryl S - 300、磷酸纤维素、Mono Q、Mono S和Superose 6五步柱色谱法。四种形式的PLC(暂定为N1、N2、N3和N4)被纯化了440 - 1400倍。在SDS - 聚丙烯酰胺凝胶电泳上,N1、N2、N3和N4的表观分子量分别为85、83、80和88 kDa。N1与针对δ1同工型的抗体发生交叉反应,而其他三种形式与针对PLC - δ1、 - γ1、 - γ2和 - β1的任何抗体均不发生交叉反应。它们水解磷脂酰肌醇(PI)、磷脂酰肌醇4 - 单磷酸(PIP)和磷脂酰肌醇4,5 - 二磷酸(PIP2),但对磷脂酰胆碱和磷脂酰乙醇胺没有任何活性。它们显示出相同的最佳pH值:PI水解为pH 6.5,PIP和PIP2水解均为pH 7.0。它们的活性绝对需要Ca2 +,PIP的最佳浓度为10(-3)-10(-5)M,PIP2的最佳浓度为10(-4)-10(-5)M。对于PI水解,N1、N2和N3需要高于10(-2)M的Ca2 +浓度,而N4即使在10(-5)M Ca2 +浓度下也显示出显著活性。通过与核PLC相同的程序,从AH7974细胞中纯化出两种形式的质膜PLC和三种形式的胞质PLC。与这三组的比较研究表明,除了N4外,所有纯化的PLC同工型都具有相似的酶学性质,N4对Mono S柱具有异常高的亲和力,并且以低浓度的Ca2 +作为PI底物时具有活性。此外,当将成年静止大鼠肝脏核的PLC同工型与部分肝切除术后再生大鼠肝脏核的PLC同工型进行比较时,仅在再生肝核中发现了一种与AH7974细胞的N4相对应的PLC同工型。从这些结果表明,生长中肝细胞 的核具有一种独特形式的PLC(N4)。

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