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心肌肌浆网(Ca2+ + Mg2+)-ATP酶的调节

Regulation of cardiac sarcoplasmic reticulum (Ca2+ + Mg2+)-ATPase.

作者信息

Shamoo A E, Joshi N B, Lockwich T

机构信息

Department of Biological Chemistry, University of Maryland, School of Medicine, Baltimore 21201.

出版信息

Mol Cell Biochem. 1988 Jul-Aug;82(1-2):45-9. doi: 10.1007/BF00242514.

Abstract

The two high affinity calcium binding sites of the cardiac (Ca2+ + Mg2+)-ATPase have been identified with the use of Eu3+. Eu3+ competes for the two high affinity calcium sites on the enzyme. With the use of laser-pulsed fluorescent spectroscopy, the environment of the two sites appear to be heterogeneous and contain different numbers of H2O molecules coordinated to the ion. The ion appears to be occluded even further in the presence of ATP. Using non-radiative energy transfer studies, we were able to estimate the distance between the two Ca2+ sites to be between 9.4 to 10.2 A in the presence of ATP. Finally, from the assumption that the calcium site must contain four carboxylic side chains to provide the 6-8 ligands needed to coordinate calcium, and based on our recently published data, we predict the peptidic backbone of the two sites.

摘要

利用铕离子(Eu3+)已鉴定出心脏(Ca2+ + Mg2+)-ATP酶的两个高亲和力钙结合位点。Eu3+竞争该酶上的两个高亲和力钙位点。通过激光脉冲荧光光谱法,这两个位点的环境似乎是异质的,且含有与离子配位的不同数量的水分子。在ATP存在的情况下,离子似乎被进一步封闭。利用非辐射能量转移研究,我们能够估计在ATP存在时两个Ca2+位点之间的距离在9.4至10.2埃之间。最后,基于钙位点必须包含四个羧基侧链以提供配位钙所需的6-8个配体这一假设,并根据我们最近发表的数据,我们预测了这两个位点的肽主链。

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