The Na+/Ca2+ exchanger protein was first isolated from cardiac sarcolemma in 1988 and cloned in 1990. This allowed study of Na+/Ca2+ exchange at the molecular level to begin. I will review the story leading to the cloning of NCX and the research that resulted from this event. This will include structure-function studies such as determination of the numbers of transmembrane segments and topological arrangement. Information on ion transport sites has been gathered from site-directed mutagenesis. The regions involved in Ca2+ regulation have been identified, analyzed, and crystallized. We have also generated genetically altered mice to study the role of NCX in the myocardium. Of special interest are mice with atrial- or ventricular-specific KO of NCX that reveal new information on the role of NCX in excitation-contraction coupling and in cardiac pacemaker activity. © Springer Science+Business Media New York 2013.
CITATION STYLE
Nicoll, D. A., Ottolia, M., Goldhaber, J. I., & Philipson, K. D. (2013). 20 Years from NCX purification and cloning: Milestones. In Advances in Experimental Medicine and Biology (Vol. 961, pp. 17–23). Springer Science and Business Media, LLC. https://doi.org/10.1007/978-1-4614-4756-6_2
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