Transient binding of an activator BH3 domain to the Bak BH3-binding groove initiates Bak oligomerization

Haiming Dai, Alyson Smith, X. Wei Meng, Paula A. Schneider, Yuan Ping Pang, Scott H. Kaufmann

Research output: Contribution to journalArticle

98 Scopus citations

Abstract

The mechanism by which the proapoptotic Bcl-2 family members Bax and Bak release cytochrome c from mitochondria is incompletely understood. In this paper, we show that activator BH3-only proteins bind tightly but transiently to the Bak hydrophobic BH3-binding groove to induce Bak oligomerization, liposome permeabilization, mitochondrial cytochrome c release, and cell death. Analysis by surface plasmon resonance indicated that the initial binding of BH3-only proteins to Bak occurred with similar kinetics with or without detergent or mitochondrial lipids, but these reagents increase the strength of the Bak-BH3-only protein interaction. Point mutations in Bak and reciprocal mutations in the BH3-only proteins not only confirmed the identity of the interacting residues at the Bak-BH3-only protein interface but also demonstrated specificity of complex formation in vitro and in a cellular context. These observations indicate that transient protein-protein interactions involving the Bak BH3-binding groove initiate Bak oligomerization and activation.

Original languageEnglish (US)
Pages (from-to)39-48
Number of pages10
JournalJournal of Cell Biology
Volume194
Issue number1
DOIs
StatePublished - Jul 11 2011

ASJC Scopus subject areas

  • Cell Biology

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