Suppr超能文献

通过胰蛋白酶切割含有磷酸化位点的片段来激活嗜盐杜氏藻质膜H(+) -ATP酶。

Activation of the Dunaliella acidophila plasma membrane H(+)-ATPase by trypsin cleavage of a fragment that contains a phosphorylation site.

作者信息

Sekler I, Weiss M, Pick U

机构信息

Department of Biochemistry, Weizmann Institute of Science, Rehovot, Israel.

出版信息

Plant Physiol. 1994 Aug;105(4):1125-32. doi: 10.1104/pp.105.4.1125.

Abstract

Trypsin treatment of purified H(+)-ATPase from plasma membranes of the extreme acidophilic alga Dunaliella acidophila enhances ATP hydrolysis and H+ pumping activities. The activation is associated with an alkaline pH shift, an increase in Vmax, and a decrease in Km(ATP). The activation is correlated with cleavage of the 100-kD ATPase polypeptide to a fragment of approximately 85 kD and the appearance of three minor hydrophobic fragments of 7 to 8 kD, which remain associated with the major 85-kD polypeptide. The N-terminal sequence of the small fragments has partial homology to residues 713 to 741 of Arabidopsis thaliana plasma membrane H(+)-ATPases. Incubation of cells with 32P-labeled orthophosphate (32Pi) results in incorporation of 32P into the ATPase 100-kD polypeptide. Trypsin treatment of the 32Pi-labeled ATPase leads to complete elimination of label from the approximately 85-kD polypeptide. Cleavage of the phosphorylated enzyme with endoproteinase Glu-C (V-8) yields a phosphorylated 12-kD fragment. Peptide mapping comparison between the 100-kD and the trypsinized 85-kD polypeptides shows that the 12-kD fragment is derived from the trypsin-cleaved part of the enzyme. The N-terminal sequence of the 12-kD fragment closely resembles a C-terminal stretch of an ATPase from another Dunaliella species. It is suggested that trypsin activation of the D. acidophila plasma membrane H(+)-ATPase results from elimination of an autoinhibitory domain at the C-terminal end of the enzyme that carries a vicinal phosphorylation site.

摘要

用胰蛋白酶处理极端嗜酸藻类杜氏盐藻质膜纯化的H(+)-ATP酶,可增强ATP水解和H+泵浦活性。这种激活作用与碱性pH值的变化、Vmax的增加以及Km(ATP)的降低有关。激活作用与100-kD ATP酶多肽裂解为约85 kD的片段以及出现三个7至8 kD的较小疏水片段有关,这些小片段仍与主要的85-kD多肽相关联。小片段的N端序列与拟南芥质膜H(+)-ATP酶的713至741位残基具有部分同源性。用32P标记的正磷酸盐(32Pi)孵育细胞会导致32P掺入ATP酶的100-kD多肽中。用胰蛋白酶处理32Pi标记的ATP酶会导致约85-kD多肽上的标记完全消除。用内蛋白酶Glu-C(V-8)切割磷酸化酶会产生一个12-kD的磷酸化片段。100-kD和经胰蛋白酶处理的85-kD多肽之间的肽图谱比较表明,12-kD片段源自酶的胰蛋白酶切割部分。12-kD片段的N端序列与另一种杜氏盐藻的ATP酶的C端序列非常相似。有人认为,胰蛋白酶对杜氏盐藻质膜H(+)-ATP酶的激活作用是由于消除了该酶C端携带邻近磷酸化位点的自抑制结构域所致。

相似文献

引用本文的文献

本文引用的文献

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验