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The Anti-Apoptotic Bcl-xL Protein, a New Piece in the Puzzle of Cytochrome C Interactome.

Authors :
Bertini, Ivano
Chevance, Soizic
Del Conte, Rebecca
Lalli, Daniela
Turano, Paola
Source :
PLoS ONE; 2011, Vol. 6 Issue 4, p1-7, 7p
Publication Year :
2011

Abstract

A structural model of the adduct between human cytochrome c and the human anti-apoptotic protein Bcl-x<subscript>L</subscript>, which defines the protein-protein interaction surface, was obtained from solution NMR chemical shift perturbation data. The atomic level information reveals key intermolecular contacts identifying new potentially druggable areas on cytochrome c and Bcl-x<subscript>L</subscript>. Involvement of residues on cytochrome c other than those in its complexes with electron transfer partners is apparent. Key differences in the contact area also exist between the Bcl-x<subscript>L</subscript> adduct with the Bak peptide and that with cytochrome c. The present model provides insights to the mechanism by which cytochrome c translocated to cytosol can be intercepted, so that the apoptosome is not assembled. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
19326203
Volume :
6
Issue :
4
Database :
Complementary Index
Journal :
PLoS ONE
Publication Type :
Academic Journal
Accession number :
61167690
Full Text :
https://doi.org/10.1371/journal.pone.0018329