Specificity of ligand binding to transport sites:: Ca2+ binding to the Ca2+ transport ATPase and its dependence on H+ and Mg2+

被引:21
|
作者
Zafar, Sufi [1 ]
Hussain, Arif [2 ]
Liu, Yueyong [3 ]
Lewis, David [3 ]
Inesi, G. [3 ]
机构
[1] IBM Corp, Thomas J Watson Res Ctr, Yorktown Hts, NY 10598 USA
[2] Univ Maryland, Med Ctr, Greenebaum Canc Ctr, Baltimore, MD 21201 USA
[3] Calif Pacific Med Ctr, Res Inst, San Francisco, CA 94107 USA
关键词
Ca2+ ATPase; Ca2+ binding; H+/Ca2+ exchange; statistical analysis;
D O I
10.1016/j.abb.2008.04.035
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ligand binding to transport sites constitutes the initial step in the catalytic cycle of transport ATPases. Here, we consider the well characterized Ca2+ ATPase of sarcoplasmic reticulum (SERCA) and describe a series of Ca2+ binding isotherms obtained by equilibrium measurements in the presence of various H+ and Mg2+ concentrations. We subject the isotherms to statistical mechanics analysis, using a model based on a minimal number of mechanistic steps. The analysis allows satisfactory fits and yields information on occupancy of the specific Ca2+ sites under various conditions. It also provides a fundamental method for analysis of binding specificity to transport sites under equilibrium conditions that lead to tightly coupled catalytic activation. (c) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:87 / 94
页数:8
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