Free Content Peptides corresponding to helices 5 and 6 of Bax can independently form large lipid pores

Authors: García-Sáez, Ana J.1; Coraiola, Manuela2; Serra, Mauro Dalla2; Mingarro, Ismael1; Müller, Peter3; Salgado, Jesús

Source: FEBS Journal, Volume 273, Number 5, March 2006 , pp. 971-981(11)

Publisher: Wiley-Blackwell

Buy & download fulltext article:

You have access to the full text article on a website external to ingentaconnect.

Please click here to view this article on Wiley Online Library.

You may be required to register and activate access on Wiley Online Library before you can obtain the full text. If you have any queries please visit Wiley Online Library

Abstract:

Proteins of the B-cell lymphoma protein 2 (Bcl2) family are key regulators of the apoptotic cascade, controlling the release of apoptotic factors from the mitochondrial intermembrane space. A helical hairpin found in the core of water-soluble folds of these proteins has been reported to be the pore-forming domain. Here we show that peptides including any of the two α-helix fragments of the hairpin of Bcl2 associated protein X (Bax) can independently induce release of large labelled dextrans from synthetic lipid vesicles. The permeability promoted by these peptides is influenced by intrinsic monolayer curvature and accompanied by fast transbilayer redistribution of lipids, supporting a toroidal pore mechanism as in the case of the full-length protein. However, compared with the pores made by complete Bax, the pores made by the Bax peptides are smaller and do not need the concerted action of tBid. These data indicate that the sequences of both fragments of the hairpin contain the principal physicochemical requirements for pore formation, showing a parallel between the permeabilization mechanism of a complex regulated protein system, such as Bax, and the much simpler pore-forming antibiotic peptides.

Keywords: amphipathic peptides; apoptosis; Bcl2 proteins; membrane proteins; toroidal pores

Document Type: Research article

DOI: http://dx.doi.org/10.1111/j.1742-4658.2006.05123.x

Affiliations: 1: Department of Biochemistry and Molecular Biology, University of Valencia, Spain 2: ITC-CNR Institute of Biophysics, Trento, Italy 3: Institut für Biologie/Biophysik, Humboldt-Universität zu Berlin, Germany

Publication date: 2006-03-01

Tools

Key

Free Content
Free content
New Content
New content
Open Access Content
Open access content
Subscribed Content
Subscribed content
Free Trial Content
Free trial content

Text size:

A | A | A | A
Share this item with others: These icons link to social bookmarking sites where readers can share and discover new web pages. print icon Print this page