Active Bax is organized at the membrane as assemblies of dimers. Two protein core domains build a stable interaction along helices 2–5. By contrast, helices 6 to 9 of Bax re-organize: they are dislodged from the core domain and adopt a dynamic configuration at the membrane. The most significant conformational change is the opening of the hairpin formed by helices 5-6 in each monomer to assemble a clamp-like dimeric structure. This new conformation is proposed to pinch the membrane bilayer forming a toroidal pore.
The model proposed by the Berlin-based scientist Enrica Bordignon and her colleagues emphasizes the significant transformation of Bax from the aqueous inactive state to the membrane-bound active state. This makes earlier models based on the permanent preservation of 5 to 6 hairpins obsolete. "If we understand how the Bax protein deforms the membrane and forms pores, we are one step closer to understanding how cells die, and thus one step closer to the development of new cancer drugs which should promote cell death," says Enrica Bordignon.
Enrica Bordignon was born in 1975 in Italy. She earned a degree in chemistry at the University of Padua, Italy, where she also completed a doctorate in physical chemistry in 2003. Her doctoral advisor was Prof. Dr. Donatella Carbonera. From 2003 to 2008 Bordignon was a postdoctoral researcher in the Prof. Dr. Heinz-Jürgen Steinhoff’s laboratory of the University of Osnabrück, where she started investigating the structure and dynamics of membrane proteins. From 2008 to 2013 she further specialized in this field while working as senior researcher in Prof. Dr. Gunnar Jeschke's laboratory at ETH Zurich in Switzerland. Bordignon has been a professor of biophysics at the Department of Physics, Freie Universität Berlin, since September 2013.
Stephanie Bleicken, Gunnar Jeschke, Carolin Stegmueller, Raquel Salvador-Gallego, Ana J. García-Sáez, Enrica Bordignon. 2014. Structural Model of Active Bax at the Membrane, in: Molecular Cell, Elsevier Inc.