Abstract
A structural model of the adduct between human cytochrome c and the human anti-apoptotic protein Bcl-xL, 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-xL. 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-xL 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. © 2011 Bertini et al.
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CITATION STYLE
Bertini, I., Chevance, S., Del Conte, R., Lalli, D., & Turano, P. (2011). The anti-apoptotic Bcl-xl protein, a new piece in the puzzle of cytochrome c interactome. PLoS ONE, 6(4). https://doi.org/10.1371/journal.pone.0018329
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