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弗瑞德红白血病细胞的(钠,钾)-ATP酶在ATP水解附近被一种内源性膜结合激酶磷酸化。

The (Na,K)-ATPase of Friend erythroleukemia cells is phosphorylated near the ATP hydrolysis by an endogenous membrane-bound kinase.

作者信息

Ling L, Cantley L

出版信息

J Biol Chem. 1984 Apr 10;259(7):4089-95.

PMID:6323456
Abstract

Friend murine erythroleukemia cells (MEL cells) contain a cAMP-independent protein kinase which phosphorylates the 100,000-Da catalytic subunit of the (Na,K)-ATPase both in living cells and in the purified plasma membrane (Yeh, L.-A., Ling, L., English, L., and Cantley, L. (1983) J. Biol. Chem. 258, 6567-6574). We have taken advantage of the selective phosphorylation of the 100,000-Da subunit in purified plasma membranes and the similarity between the proteolysis patterns of the MEL cell and dog kidney (Na,K)-ATPase to map the site of kinase phosphorylation on the MEL cell enzyme. The chymotryptic and tryptic cleavage sites of the dog kidney (Na,K)-ATPase have previously been located (Castro, J., and Farley, R. A. (1979) J. Biol. Chem. 254, 2221-2228). The 100,000-Da catalytic subunits of the dog kidney and MEL cell enzymes were specifically labeled at the active site aspartate residue by incubation with (32P)orthophosphate in the presence of Mg2+ and ouabain. Digestion of these two enzymes with chymotrypsin or trypsin revealed similar active site aspartate containing proteolytic fragments indicating a similar structure for the two enzymes. Chymotryptic digestions of MEL cell (Na,K)-ATPase labeled in vitro with [gamma-32P]ATP localize the region of kinase phosphorylation to within a 35,000-Da peptide derived from the middle of the 100,000-Da subunit. Tryptic digestion of the MEL cell plasma membranes degraded the 100,000-Da subunit to an NH2-terminal 43,000-Da peptide which contained the active site aspartate but which did not contain the kinase-labeled region. These results further locate the region of kinase phosphorylation to the COOH-terminal half of the 35,000-Da chymotryptic peptide. This location places the site of phosphorylation between the active site aspartate residue which accepts the phosphate of ATP during turnover and an ATP-binding site which has previously been located by labeling with fluorescein 5'-isothiocyanate (Carilli, C. T., Farley, R. A., Perlman, D. M., and Cantley, L. C. (1982) J. Biol. Chem. 257, 5601-5606). Phosphorylation of the (Na,K)-ATPase in this region may serve to regulate the activity of this enzyme.

摘要

弗瑞德小鼠红白血病细胞(MEL细胞)含有一种不依赖cAMP的蛋白激酶,该激酶在活细胞以及纯化的质膜中均可使(Na,K)-ATP酶的100,000道尔顿催化亚基发生磷酸化(叶,L.-A.,凌,L.,英格利希,L.,和坎特利,L.(1983)《生物化学杂志》258,6567 - 6574)。我们利用纯化质膜中100,000道尔顿亚基的选择性磷酸化以及MEL细胞与犬肾(Na,K)-ATP酶蛋白水解模式的相似性,来确定MEL细胞酶上激酶磷酸化的位点。犬肾(Na,K)-ATP酶的胰凝乳蛋白酶和胰蛋白酶切割位点此前已确定(卡斯特罗,J.,和法利,R. A.(1979)《生物化学杂志》254,2221 - 2228)。通过在Mg2 +和哇巴因存在的情况下与(32P)正磷酸盐一起温育,犬肾和MEL细胞酶的100,000道尔顿催化亚基在活性位点天冬氨酸残基处被特异性标记。用胰凝乳蛋白酶或胰蛋白酶消化这两种酶,发现含有相似活性位点天冬氨酸的蛋白水解片段,表明这两种酶具有相似的结构。用[γ - 32P]ATP在体外标记的MEL细胞(Na,K)-ATP酶经胰凝乳蛋白酶消化后,将激酶磷酸化区域定位在源自100,000道尔顿亚基中部的一个35,000道尔顿肽段内。对MEL细胞质膜进行胰蛋白酶消化,将100,000道尔顿亚基降解为一个NH2末端的43,000道尔顿肽段,该肽段含有活性位点天冬氨酸,但不包含激酶标记区域。这些结果进一步将激酶磷酸化区域定位到35,000道尔顿胰凝乳蛋白酶肽段的COOH末端一半。该位置将磷酸化位点置于在周转过程中接受ATP磷酸基团的活性位点天冬氨酸残基与先前通过用异硫氰酸荧光素5'-标记确定的ATP结合位点之间(卡里利,C. T.,法利,R. A.,珀尔曼,D. M.,和坎特利,L. C.(1982)《生物化学杂志》257,5601 - 5606)。该区域的(Na,K)-ATP酶磷酸化可能用于调节该酶的活性。

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