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Structure-based reassessment of the caveolin signaling model: do caveolae regulate signaling through caveolin-protein
Brett M Collins1, Melissa J Davis, John F Hancock
1The Institute for Molecular Bioscience, The University of Queensland, Brisbane, QLD 4072, Australia. b.collins@imb.uq.edu.au
Abstract:
Caveolin proteins drive formation of caveolae, specialized cell-surface microdomains that influence cell signaling. Signaling proteins are proposed to use conserved caveolin-binding motifs (CBMs) to associate with caveolae via the caveolin scaffolding domain (CSD). However, structural and bioinformatic analyses argue against such direct physical interactions: in the majority of signaling proteins, the CBM is buried and inaccessible. Putative CBMs do not form a common structure for caveolin recognition, are not enriched among caveolin-binding proteins, and are even more common in yeast, which lack caveolae. We propose that CBM/CSD-dependent interactions are unlikely to mediate caveolar signaling, and the basis for signaling effects should therefore be reassessed.
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