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环磷酸腺苷(cAMP)依赖性蛋白激酶催化亚基相互作用的抑制蛋白。复合物形成参数。

The inhibitor protein of the cAMP-dependent protein kinase-catalytic subunit interaction. Parameters of complex formation.

作者信息

Van Patten S M, Fletcher W H, Walsh D A

出版信息

J Biol Chem. 1986 Apr 25;261(12):5514-23.

PMID:3082887
Abstract

The formation of a complex between the catalytic subunit of the cAMP-dependent protein kinase and the Inhibitor Protein of this enzyme has been examined by means of nondenaturing gel electrophoresis. Two forms of complex were identified, both containing a 1:1 molar ratio of the component proteins. The formation of the major of the two forms is markedly enhanced by the presence of nucleotide triphosphate and divalent cation. Either Mg2+ or Mn2+ serves to promote complex formation. With Mg2+, only ATP is effective for enhancing complex formation, whereas with Mn2+ complex formation occurs to an equal extent with ATP, GTP, ITP, and adenyl-5'-yl imidodiphosphate. The formation of the two complexes is only minimally dependent upon nucleotide triphosphate. It is suggested that the two types of complex are a result of different species of catalytic subunit. Two principal forms of the complex have been detected occurring maximally in approximately a 2.5:1 ratio. In the accompanying paper (Fletcher, W.H., Van Patten, S.M., Cheng, H-C., and Walsh, D.A. (1986) J. Biol. Chem. 261, 5504-5513), we have described the use of a fluoresceinated derivative of catalytic subunit as a cytochemical probe to localize the Inhibitor Protein and the regulatory subunit of the protein kinase. The integrity of this fluorophore has been further characterized using the method of examining catalytic subunit-Inhibitor Protein interaction delineated here.

摘要

通过非变性凝胶电泳法研究了环磷酸腺苷依赖性蛋白激酶催化亚基与该酶抑制蛋白之间复合物的形成。鉴定出两种复合物形式,两者均含有等摩尔比的组成蛋白。三磷酸核苷酸和二价阳离子的存在显著增强了两种形式中主要形式的形成。Mg2+或Mn2+均有助于促进复合物的形成。对于Mg2+,只有ATP能有效增强复合物的形成,而对于Mn2+,ATP、GTP、ITP和腺苷-5'-亚氨基二磷酸在同等程度上促进复合物的形成。两种复合物的形成仅轻微依赖于三磷酸核苷酸。有人提出这两种复合物类型是不同种类催化亚基的结果。已检测到两种主要形式的复合物,其最大比例约为2.5:1。在随附的论文中(弗莱彻,W.H.,范·帕滕,S.M.,程,H-C.,和沃尔什,D.A.(1986年)《生物化学杂志》261,5504 - 5513),我们描述了使用催化亚基的荧光素化衍生物作为细胞化学探针来定位蛋白激酶的抑制蛋白和调节亚基。使用此处描述的检测催化亚基 - 抑制蛋白相互作用的方法进一步表征了这种荧光团的完整性。

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