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单克隆抗体对人血小板中蛋白激酶C两种亚型形式的识别。

Monoclonal antibody recognition of two subtype forms of protein kinase C in human platelets.

作者信息

Watanabe M, Hagiwara M, Onoda K, Hidaka H

机构信息

Department of Molecular and Cellular Pharmacology, Mie University School of Medicine, Japan.

出版信息

Biochem Biophys Res Commun. 1988 Apr 29;152(2):642-8. doi: 10.1016/s0006-291x(88)80087-1.

Abstract

Using a hydroxylapatite column chromatographic technique, we obtained the evidence for two subtype forms of protein kinase C in human platelets. These subtypes had a similar chromatographic property to Type II, Type III protein kinase C from the rabbit brain. In addition, in monoclonal antibodies (MC-1a, 2a, 3a) (1) which reacted with specifically Type I, II, III rabbit brain protein kinase C, respectively, only MC-2a and MC-3a reacted with human platelet protein kinase C. All these brain and platelet subtypes have a similar Km value for ATP, the range being from 8.0 to 20.0 microM and a similar IC50 value with regard to the effect of the protein kinase C inhibitor, H-7. Thus, the possibility that specific functions of platelet may be derived from a deficiency of Type I protein kinase C warrants attention.

摘要

利用羟基磷灰石柱色谱技术,我们获得了人血小板中蛋白激酶C两种亚型形式的证据。这些亚型与兔脑中的II型、III型蛋白激酶C具有相似的色谱特性。此外,在分别与兔脑I型、II型、III型蛋白激酶C特异性反应的单克隆抗体(MC-1a、2a、3a)中,只有MC-2a和MC-3a与人血小板蛋白激酶C发生反应。所有这些脑和血小板亚型对ATP的Km值相似,范围为8.0至20.0微摩尔,并且在蛋白激酶C抑制剂H-7的作用方面具有相似的IC50值。因此,血小板的特定功能可能源于I型蛋白激酶C缺乏的可能性值得关注。

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