Submit Manuscript  

Article Details


V-ATPase Subunit Interactions: The Long Road to Therapeutic Targeting

[ Vol. 13 , Issue. 2 ]

Author(s):

Norbert Kartner and Morris F. Manolson   Pages 164 - 179 ( 16 )

Abstract:


Over the last three decades, V-ATPases have emerged from the obscurity of poorly understood membrane proton transport phenomena to being recognized as ubiquitous proton pumps that underlie vital cellular processes in all eukaryotic and many prokaryotic cells. These exquisitely complex molecular motors also engage in diverse specialized roles contributing to development, tissue function and pH homeostasis within complex organisms. Increasingly, mutations and misappropriation of V-ATPase function have been linked to diseases, ranging from sclerosing bone pathologies and renal tubular acidosis to bone-loss disorders and cancer metastasis. Much remains to be learned about the details of V-ATPase cell and molecular biology; nevertheless, interest in V-ATPases as potential therapeutic targets has burgeoned in recent years. In this review, we present a history of our involvement and contributions to the understanding of V-ATPase structure and function and our nascent and ongoing contributions to translating the knowledge gained from basic research on the nature of V-ATPases into tools for drug discovery. We focus here primarily on the treatment of bone-loss pathologies, like osteoporosis, and present proof-of-concept for a drug screening strategy based on targeting a3-B2 subunit interactions within the V-ATPase complex.

Keywords:

Bone loss pathology, drug discovery, high throughput screening, membrane transport, osteolysis, osteoporosis, protein interaction, tumor metastasis, vacuolar proton-translocating ATPase, vesicular proton pump, V-type H+-ATPase

Affiliation:

Bonelab, Dental Research Institute, Faculty of Dentistry, University of Toronto, Toronto, ON M5G 1G6, Canada.



Read Full-Text article