Application of cryo-electron microscopy for investigation of Bax-induced pores in apoptosis

• Published in: Nanotechnology reviews (Berlin) Vol. 6; no. 1; pp. 47 - 55
• Main Author: Kuwana, Tomomi
• Format: Journal Article
• Language: English
• Published: Berlin De Gruyter 01.02.2017; Walter de Gruyter GmbH
• Subjects: Apoptosis; Atomic structure; BAK protein; Bax; BAX protein; Cancer; cryo-EM; Data processing; Electron microscopes; Electron microscopy; Lipids; Liposomes; Major outer membrane protein; Membrane structure; Membrane structures; Membrane vesicles; Membranes; Mitochondria; Molecular modelling; Pores; Transmission electron microscopy; Vesicles
• ISSN: 2191-9089; 2191-9097
• DOI: 10.1515/ntrev-2016-0070

Mitochondrial outer membrane permeabilization (MOMP) is a critical step in apoptosis, the molecular mechanisms of which have been a subject of intensive study. This process is important for therapeutic intervention in various diseases, such as cancer. Pro-apoptotic Bax and Bak are functionally redundant and structurally homologous. When activated at the mitochondrial outer membrane, they cause the membrane to permeabilize and release apoptogenic proteins from the intermembrane space. To unravel the molecular mechanisms of this unique and important event, we systematically reduced the experimental system. Simple outer membrane vesicles and liposomes recapitulated many features of MOMP. Although conventional transmission electron microscopy could not detect any membrane changes during MOMP in these vesicles, cryo-electron microscopy successfully revealed Bax-induced delicate pores, owing to its ability to preserve native, hydrated membrane structure. The data are consistent with the idea that Bax is unfolded and embedded in the bilayer and deforms the membrane to form a large pore. Together with the biochemical and structure data in the literature, we now have more comprehensive models of the key function of Bax. We hope that new tools, such as lipid nanodiscs, will give us an atomic-level resolution and finally solve Bax structure in the membrane, where it functions.