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204千道尔顿的平滑肌肌球蛋白重链在完整细胞中被酪蛋白激酶II在靠近羧基末端的一个丝氨酸上磷酸化。

The 204-kDa smooth muscle myosin heavy chain is phosphorylated in intact cells by casein kinase II on a serine near the carboxyl terminus.

作者信息

Kelley C A, Adelstein R S

机构信息

Laboratory of Molecular Cardiology, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland 20892.

出版信息

J Biol Chem. 1990 Oct 15;265(29):17876-82.

PMID:2170399
Abstract

The heavy chain of smooth muscle myosin was found to be phosphorylated following immunoprecipitation from cultured bovine aortic smooth muscle cells. Of a variety of serine/threonine kinases assayed, only casein kinase II and calcium/calmodulin-dependent protein kinase II phosphorylated the smooth muscle myosin heavy chain to a significant extent in vitro. Two-dimensional maps of tryptic peptides derived from heavy chains phosphorylated in cultured cells revealed one major and one minor phosphopeptide. Identical tryptic peptide maps were obtained from heavy chains phosphorylated in vitro with casein kinase II but not with calcium/calmodulin-dependent protein kinase II. Of note, the 204-kDa smooth muscle myosin heavy chain but not the 200-kDa heavy chain isoform was phosphorylated by casein kinase II. Partial sequence of the tryptic phosphopeptides generated following phosphorylation by casein kinase II yielded Val-Ile-Glu-Asn-Ala-Asp-Gly-Ser*-Glu-Glu-Glu-Val. The Ser* represents the Ser(PO4) which is in an acidic environment, as is typical for casein kinase II phosphorylation sites. By comparison with the deduced amino acid sequence for rabbit uterine smooth muscle myosin (Nagai, R., Kuro-o, M., Babij, P., and Periasamy, M. (1989) J. Biol. Chem. 264, 9734-9737), we have localized the phosphorylated serine residue to the non-helical tail of the 204-kDa isoform of the smooth muscle myosin heavy chain. The ability of the 204-kDa isoform, but not the 200-kDa isoform, to serve as a substrate for casein kinase II suggests that these two isoforms can be regulated differentially.

摘要

从培养的牛主动脉平滑肌细胞中进行免疫沉淀后,发现平滑肌肌球蛋白重链发生了磷酸化。在检测的多种丝氨酸/苏氨酸激酶中,只有酪蛋白激酶II和钙/钙调蛋白依赖性蛋白激酶II在体外能使平滑肌肌球蛋白重链发生显著磷酸化。来源于培养细胞中磷酸化重链的胰蛋白酶肽段的二维图谱显示有一个主要磷酸肽段和一个次要磷酸肽段。用酪蛋白激酶II体外磷酸化重链得到了相同的胰蛋白酶肽图谱,而用钙/钙调蛋白依赖性蛋白激酶II则未得到。值得注意的是,204 kDa的平滑肌肌球蛋白重链可被酪蛋白激酶II磷酸化,而200 kDa的重链异构体则不能。酪蛋白激酶II磷酸化后产生的胰蛋白酶磷酸肽段的部分序列为Val-Ile-Glu-Asn-Ala-Asp-Gly-Ser*-Glu-Glu-Glu-Val。Ser*代表处于酸性环境中的Ser(PO4),这是酪蛋白激酶II磷酸化位点的典型特征。通过与兔子宫平滑肌肌球蛋白的推导氨基酸序列(Nagai, R., Kuro-o, M., Babij, P., and Periasamy, M. (1989) J. Biol. Chem. 264, 9734 - 9737)进行比较,我们已将磷酸化的丝氨酸残基定位到204 kDa平滑肌肌球蛋白重链异构体的非螺旋尾部。204 kDa异构体而非200 kDa异构体作为酪蛋白激酶II底物的能力表明这两种异构体可能受到不同的调节。

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