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J Biol Chem. November 4, 2011; 286 (44): 38177-83.

Ouabain binding site in a functioning Na+/K+ ATPase.

Sandtner W , Egwolf B , Khalili-Araghi F , Sánchez-Rodríguez JE , Roux B , Bezanilla F , Holmgren M .

The Na(+)/K(+) ATPase is an almost ubiquitous integral membrane protein within the animal kingdom. It is also the selective target for cardiotonic derivatives, widely prescribed inhibitors for patients with heart failure. Functional studies revealed that ouabain-sensitive residues distributed widely throughout the primary sequence of the protein. Recently, structural work has brought some consensus to the functional observations. Here, we use a spectroscopic approach to estimate distances between a fluorescent ouabain and a lanthanide binding tag (LBT), which was introduced at five different positions in the Na(+)/K(+) ATPase sequence. These five normally functional LBT-Na(+)/K(+) ATPase constructs were expressed in the cell membrane of Xenopus laevis oocytes, operating under physiological internal and external ion conditions. The spectroscopic data suggest two mutually exclusive distances between the LBT and the fluorescent ouabain. From the estimated distances and using homology models of the LBT-Na(+)/K(+) ATPase constructs, approximate ouabain positions could be determined. Our results suggest that ouabain binds at two sites along the ion permeation pathway of the Na(+)/K(+) ATPase. The external site (low apparent affinity) occupies the same region as previous structural findings. The high apparent affinity site is, however, slightly deeper toward the intracellular end of the protein. Interestingly, in both cases the lactone ring faces outward. We propose a sequential ouabain binding mechanism that is consistent with all functional and structural studies.

PubMed ID: 21911500
PMC ID: PMC3207469
Article link: J Biol Chem.
Grant support: R01-GM030376 NIGMS NIH HHS , R01-GM062342 NIGMS NIH HHS , U54-GM087519 NIGMS NIH HHS , ZIA NS002993-10 NINDS NIH HHS , U54 GM087519 NIGMS NIH HHS , ZIA NS002993-10 Intramural NIH HHS, R01 GM062342 NIGMS NIH HHS , R01 GM030376 NIGMS NIH HHS

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, 2004, Pubmed[+]

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