Journal article
Ensemble Properties of Bax Determine Its Function
AY Robin, S Iyer, RW Birkinshaw, J Sandow, A Wardak, CS Luo, M Shi, AI Webb, PE Czabotar, RM Kluck, PM Colman
Structure | Published : 2018
Abstract
BAX and BAK are essential mediators of intrinsic apoptosis that permeabilize the mitochondrial outer membrane. BAX activation requires its translocation from cytosol to mitochondria where conformational changes cause its oligomerization. To better understand the critical step of translocation, we examined its blockade by mutation near the C terminus (P168G) or by antibody binding near the N terminus. Similarities in the crystal structures of wild-type and BAX P168G but significant other differences suggest that cytosolic BAX exists as an ensemble of conformers, and that the distribution of conformers within the ensemble determines the different functions of wild-type and mutant proteins. We ..
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Funding Acknowledgements
Studies supported by grants and fellowships from the NHMRC, the Australian Cancer Research Foundation, the Leukemia and Lymphoma Society (US), Lady Tata Memorial Trust, and the Victorian State Government Operational Infrastructure Support and the Australian Government NHMRC IRIIS. We thank Tony Burgess, Shenggen Yao, Jeff Babon, Matthew Call, and Grant Dewson for discussions, and Robert Ninnis for input into the HDX-MS analysis. Crystallization experiments were performed at the CSIRO C3 Crystallisation Center, and diffraction data were collected at the Australian Synchrotron.