K.-S. Csizi, A.E. Frackowiak, et al.
Biomicrofluidics
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. © 2008 Elsevier Inc. All rights reserved.
K.-S. Csizi, A.E. Frackowiak, et al.
Biomicrofluidics
Martin Zimmermann, Patrick Hunziker, et al.
Biomedical Microdevices
Roger D. Traub, Miles A. Whittington, et al.
Reviews in the Neurosciences
E.W. Grundke, D. Henderson, et al.
Molecular Physics