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

被引:38
作者
Bertini, Ivano [1 ,2 ]
Chevance, Soizic [1 ]
Del Conte, Rebecca [1 ]
Lalli, Daniela [1 ,2 ]
Turano, Paola [1 ,2 ]
机构
[1] Univ Florence, Magnet Resonance Ctr CERM, Florence, Italy
[2] Univ Florence, Dept Chem, Florence, Italy
关键词
BCL-X-L; ESCHERICHIA-COLI; PEPTIDE COMPLEX; CELL-SURVIVAL; BINDING; FAMILY; NMR; ACTIVATION; REGULATORS; CASPASE-9;
D O I
10.1371/journal.pone.0018329
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
A structural model of the adduct between human cytochrome c and the human anti-apoptotic protein Bcl-x(L), 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(L). 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(L) 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.
引用
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页数:7
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