二核苷多磷酸对酪蛋白激酶II的抑制作用。

Enzyme & protein Pub Date : 1993-01-01 DOI:10.1159/000468651
S Pype, H Slegers
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引用次数: 7

摘要

在我们寻找青蒿中酪蛋白激酶II (CKII)的潜在抑制剂的过程中,我们已经表明,二核苷多磷酸是这种普遍存在的蛋白激酶的一类新型效应器。P1,P4-di(guanosine-5’)-tetraphosphate (Gp4G)是比P1,P4-di(adenosine-5’)-tetraphosphate (Ap4A)更好的CKII抑制剂。当GTP代替ATP作为磷酸供体时,这两种效应物的抑制作用更强。CKII的抑制作用随着连接鸟苷/腺苷部分的磷酸盐数量的增加而增加(n = 2-6)。Ap4A不与蛋白质底物竞争,导致表观KmATP增加和表观VmATP减少,表明对ATP的抑制是混合类型的。
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Inhibition of casein kinase II by dinucleoside polyphosphates.

In our search for potential inhibitors of casein kinase II (CKII) in Artemia, we have shown that dinucleoside polyphosphates are a novel class of effectors for this ubiquitous protein kinase. P1,P4-di(guanosine-5')-tetraphosphate (Gp4G) is a better CKII inhibitor than P1,P4-di(adenosine-5')-tetraphosphate (Ap4A). The inhibition by both effectors is more potent when GTP is used as phosphate donor instead of ATP. The inhibition of CKII increases with the number of phosphates linking the guanosine/adenosine moieties (for n = 2-6). Ap4A does not compete with the protein substrate and causes an increase in the apparent KmATP and a decrease in the apparent VmATP, indicating a mixed type of inhibition with respect to ATP.

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