Suppr超能文献

来自质膜钙泵ATP酶的C末端、类钙调蛋白调节结构域。

A C-terminal, calmodulin-like regulatory domain from the plasma membrane Ca2+-pumping ATPase.

作者信息

Brandt P, Zurini M, Neve R L, Rhoads R E, Vanaman T C

机构信息

Department of Biochemistry, University of Kentucky Medical Center, Lexington 40536-0084.

出版信息

Proc Natl Acad Sci U S A. 1988 May;85(9):2914-8. doi: 10.1073/pnas.85.9.2914.

Abstract

A cDNA that encodes what appears to be the inhibitory domain of the plasma membrane calcium-pumping ATPase (Ca2+-ATPase) has been isolated by screening a lambda gt11 bovine brain cDNA library with antibodies prepared against the human erythrocyte membrane Ca2+-ATPase. This screening resulted in isolation of a bacteriophage containing a 1.5-kilobase cDNA insert encoding a 71-residue polypeptide, the remainder being a large 3' terminal noncoding region. A portion of this deduced peptide sequence was identical to that of a peptide isolated from a V8 protease digest of the human erythrocyte Ca2+-ATPase except for 1 residue. Antibodies purified by immunoabsorption to the fusion protein containing this cDNA-encoded polypeptide reacted only with those fragments of a limited trypsin digest of the human erythrocyte Ca2+-ATPase that contain the inhibitory domain. Moreover, these antibodies were able to partially stimulate basal enzyme activity and block further activation by calmodulin. The encoded polypeptide bears homology to the glutamic acid-rich regions N-terminal to the Ca2+-binding loops of calmodulin and to a lesser extent with the loops themselves. This encoded polypeptide also represents the C terminus of the Ca2+-ATPase. Portions of the isolated cDNA were homologous to the 3' noncoding region of the sarcoplasmic reticulum Ca2+-ATPase cDNA, indicating a possible mechanism for the evolution of these distinct membrane Ca2+ pumps.

摘要

通过用针对人红细胞膜钙泵ATP酶(Ca2+-ATP酶)制备的抗体筛选λgt11牛脑cDNA文库,分离出了一个编码质膜钙泵ATP酶抑制结构域的cDNA。该筛选导致分离出一种噬菌体,其含有一个1.5千碱基的cDNA插入片段,编码一个71个氨基酸残基的多肽,其余部分是一个大的3'末端非编码区。该推导肽序列的一部分与从人红细胞Ca2+-ATP酶的V8蛋白酶消化产物中分离出的一种肽的序列相同,仅一个残基不同。通过免疫吸附纯化的针对含有该cDNA编码多肽的融合蛋白的抗体,仅与人红细胞Ca2+-ATP酶有限胰蛋白酶消化产物中含有抑制结构域的那些片段发生反应。此外,这些抗体能够部分刺激基础酶活性并阻断钙调蛋白的进一步激活。编码的多肽与钙调蛋白Ca2+结合环N端富含谷氨酸的区域具有同源性,与这些环本身的同源性较低。该编码多肽也代表Ca2+-ATP酶的C末端。分离出的cDNA的部分与肌浆网Ca2+-ATP酶cDNA的3'非编码区同源,表明了这些不同的膜钙泵进化的一种可能机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e5f/280113/7f7f389fc301/pnas00261-0044-a.jpg

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