| Literature DB >> 27932064 |
Katia Cosentino1, Ana J García-Sáez2.
Abstract
Bax and its homolog Bak are key regulators of the mitochondrial pathway of apoptosis. On cell stress Bax and Bak accumulate at distinct foci on the mitochondrial surface where they undergo a conformational change, oligomerize, and mediate cytochrome c release, leading to cell death. The molecular mechanisms of Bax and Bak assembly and mitochondrial permeabilization have remained a longstanding question in the field. Recent structural and biophysical studies at several length scales have shed light on key aspects of Bax and Bak function that have shifted how we think this process occurs. These discoveries reveal an unexpected molecular mechanism in which Bax (and likely Bak) dimers assemble into oligomers with an even number of molecules that fully or partially delineate pores of different sizes to permeabilize the mitochondrial outer membrane (MOM) during apoptosis.Entities:
Keywords: Bax; Bcl-2 proteins; apoptosis; cell death; mitochondrial outer membrane permeabilization; pore-forming proteins
Mesh:
Substances:
Year: 2016 PMID: 27932064 PMCID: PMC5898608 DOI: 10.1016/j.tcb.2016.11.004
Source DB: PubMed Journal: Trends Cell Biol ISSN: 0962-8924 Impact factor: 20.808