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CK2α/CK1α嵌合体对CK2β亚基的调控敏感。

CK2alpha/CK1alpha chimeras are sensitive to regulation by the CK2beta subunit.

作者信息

Jedlicki Ana, Allende Catherine C, Allende Jorge E

机构信息

Programa de Biología Celular y Molecular, ICBM, Facultad de Medicina, Universidad de Chile, Independencia 1027, 8380453, Santiago, Chile.

出版信息

Mol Cell Biochem. 2008 Sep;316(1-2):25-35. doi: 10.1007/s11010-008-9825-2. Epub 2008 Jul 12.

Abstract

The effect of CK2beta on the activity of CK2alpha and other protein kinases that can bind this regulatory subunit is not fully understood. In an attempt to improve our understanding of this effect, chimeras of CK2alpha and CK1alpha have been constructed. These chimeras contain different portions of the CK2alpha amino terminal region that are involved in the interaction with CK2beta to form CK2 tetramers. In the case of chimeras 1 and 2, the portions of CK2alpha replace the corresponding segments of CK1alpha. In the case of chimera 3, the fragment of CK2alpha is added to the whole CK1alpha molecule with the exception of the initial methionine. Chimera 3 has 8% of the activity of CK1alphaWT, while chimeras 1 and 2 are 3 orders of magnitude less active than CK1alphaWT. All three chimeras bind tightly to CK2beta, but only chimeras 1 and 2 are significantly stimulated in their capacity to phosphorylate casein and canonical peptide substrates by addition of the regulatory subunit. No stimulation was observed with phosvitin or non-canonical peptides derived from beta-catenin. CK2beta protects chimeras 1 and 2 from thermal inactivation. Chimera 2 can phosphorylate CK2beta and autophosphorylate; however, salt concentrations above 150 mM NaCl eliminate the phosphorylation of CK2beta but not the autophosphorylation of chimera 2. Similarly, high salt decrease the stimulatory effect of CK2beta on the phosphorylation of casein.

摘要

CK2β对CK2α及其他可结合该调节亚基的蛋白激酶活性的影响尚未完全明确。为增进对这种影响的理解,构建了CK2α与CK1α的嵌合体。这些嵌合体包含CK2α氨基末端区域中参与与CK2β相互作用以形成CK2四聚体的不同部分。对于嵌合体1和2,CK2α的部分取代了CK1α的相应片段。对于嵌合体3,CK2α的片段添加到了整个CK1α分子上,但起始甲硫氨酸除外。嵌合体3具有CK1αWT活性的8%,而嵌合体1和2的活性比CK1αWT低3个数量级。所有三种嵌合体都能紧密结合CK2β,但只有嵌合体1和2在添加调节亚基后,其磷酸化酪蛋白和典型肽底物的能力受到显著刺激。对于卵黄高磷蛋白或源自β-连环蛋白的非典型肽,未观察到刺激作用。CK2β可保护嵌合体1和2免受热失活。嵌合体2可磷酸化CK2β并进行自身磷酸化;然而,NaCl浓度高于150 mM时会消除CK2β的磷酸化,但不会消除嵌合体2的自身磷酸化。同样,高盐会降低CK2β对酪蛋白磷酸化的刺激作用。

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