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8-叠氮鸟苷3',5'-环一磷酸作为环鸟苷酸依赖性蛋白激酶的光亲和标记物的合成与应用。

Synthesis and use of 8-azidoguanosine 3',5'-cyclic monophosphate as photoaffinity label for cyclic GMP-dependent protein kinase.

作者信息

Geahlen R L, Haley B E, Krebs E G

出版信息

Proc Natl Acad Sci U S A. 1979 May;76(5):2213-7. doi: 10.1073/pnas.76.5.2213.

Abstract

8-Azidoguanosine 3',5'-cyclic monophosphate (8-N3cGMP) has been synthesized for use as a photoactive probe for the labeling of cGMP receptors. The ability of 8-N3cGMP to be bound at specific cGMP binding sites was demonstrated by its ability to activate cGMP-dependent protein kinase isolated from bovine lung (Ka = 1.1 x 10(-7) M) and to inhibit competitively the binding of [3H] cGMP to the enzyme [Kd (8 N3GMP)/Kd (cGMP) = 6]. Photolysis of 8-N3[32P]cGMP in the presence of a crude enzyme preparation resulted in the covalent attachment of analog to cGMP-dependent protein kinase. Half-maximal labeling occurred at 2.2 x 10(-7) M. The incorporation of the analog was completely inhibited by the addition of cGMP.

摘要

8-叠氮鸟苷3',5'-环一磷酸(8-N3cGMP)已被合成用作标记cGMP受体的光活性探针。8-N3cGMP在特定cGMP结合位点结合的能力通过其激活从牛肺中分离的cGMP依赖性蛋白激酶的能力得到证明(Ka = 1.1 x 10(-7) M),并竞争性抑制[3H]cGMP与该酶的结合[Kd(8 N3GMP)/Kd(cGMP) = 6]。在粗酶制剂存在下对8-N3[32P]cGMP进行光解导致类似物与cGMP依赖性蛋白激酶发生共价连接。半最大标记发生在2.2 x 10(-7) M。加入cGMP可完全抑制类似物的掺入。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b10d/383568/d3336cad26f4/pnas00005-0133-a.jpg

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