Investigation of the Bcl-2 multimerisation process: Structural and functional implications

被引:54
作者
Camperchioli, Alessia [2 ]
Mariani, Marisa [2 ]
Bartollino, Silvia [2 ]
Petrella, Lella [2 ]
Persico, Marco [1 ]
Orteca, Nausicaa [1 ]
Scambia, Giovanni [2 ]
Shahabi, Shohreh [3 ]
Ferlini, Cristiano [1 ,2 ,3 ]
Fattorusso, Caterina [1 ]
机构
[1] Univ Naples Federico 2, Fac Pharm, Dept Nat Prod Chem, Lab Computat Chem, I-80131 Naples, Italy
[2] Univ Sacred Hearth, Mol Oncol Lab, I-86100 Campobasso, Italy
[3] Danbury Hosp Res Inst, Danbury, CT 06810 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH | 2011年 / 1813卷 / 05期
关键词
Bcl-2; structure/function; Multimeric protein complexes; Apoptosis; INDUCED APOPTOSIS; FAMILY; PROTEIN; CHANNEL; DOMAIN; HOMODIMERIZATION; CLEAVAGE; COMPLEX; DEATH; CELLS;
D O I
10.1016/j.bbamcr.2011.02.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Bcl-2 plays a prominent role in regulating the function of mitochondria during respiration and in determining the threshold of apoptotic sensitivity. Despite its relevance, the mechanism through which these processes are achieved is still unknown. Using surface plasmon resonance technology to monitor Bcl-2 multimerisation we discovered that a simple dimeric model does not fit with experimental data. A molecular model of the experimentally observed Bcl-2 homomeric complex has been developed. Accordingly, using a panel of mutants we identified in the loop a critical region for the process of Bcl-2 multimerisation. Our results indicate that the Bcl-2 loop posttranscriptional changes can modulate its ability to make homo and hetero-complexes, ultimately leading to functional modulation, suggesting an intriguing relationship between the ability of Bcl-2 to form multimeric complexes and its multi-functional role as a membrane channel. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:850 / 857
页数:8
相关论文
共 33 条
[1]
The Bcl-2 protein family: Arbiters of cell survival [J].
Adams, JM ;
Cory, S .
SCIENCE, 1998, 281 (5381) :1322-1326
[2]
Expresso: automatic incorporation of structural information in multiple sequence alignments using 3D-coffee [J].
Armougom, Fabrice ;
Moretti, Sebastien ;
Poirot, Olivier ;
Audic, Stephane ;
Dumas, Pierre ;
Schaeli, Basile ;
Keduas, Vladimir ;
Notredame, Cedric .
NUCLEIC ACIDS RESEARCH, 2006, 34 :W604-W608
[3]
Posttranslational modifications of Bcl2 family members - a potential therapeutic target for human malignancy [J].
Basu, A ;
DuBois, G ;
Haldar, S .
FRONTIERS IN BIOSCIENCE-LANDMARK, 2006, 11 :1508-1521
[4]
Identification of a novel regulatory domain in Bcl-x(L) and Bcl-2 [J].
Chang, BS ;
Minn, AJ ;
Muchmore, SW ;
Fesik, SW ;
Thompson, CB .
EMBO JOURNAL, 1997, 16 (05) :968-977
[5]
Conversion of Bcl-2 to a Bax-like death effector by caspases [J].
Cheng, EHY ;
Kirsch, DG ;
Clem, RJ ;
Ravi, R ;
Kastan, MB ;
Bedi, A ;
Ueno, K ;
Hardwick, JM .
SCIENCE, 1997, 278 (5345) :1966-1968
[6]
Bcl-2 is a monomeric protein:: prevention of homodimerization by structural constraints [J].
Conus, S ;
Kaufmann, T ;
Fellay, I ;
Otter, I ;
Rossé, T ;
Borner, C .
EMBO JOURNAL, 2000, 19 (07) :1534-1544
[7]
Cleavage of Bcl-2 in oxidant- and cisplatin-induced apoptosis of human melanoma cells [J].
Del Bello, B ;
Valentini, MA ;
Zunino, F ;
Comporti, M ;
Maellaro, E .
ONCOGENE, 2001, 20 (33) :4591-4595
[8]
Cleavage of Bcl-2 is an early event in chemotherapy-induced apoptosis of human myeloid leukemia cells [J].
Fadeel, B ;
Hassan, Z ;
Hellström-Lindberg, E ;
Henter, JI ;
Orrenius, S ;
Zhivotovsky, B .
LEUKEMIA, 1999, 13 (05) :719-728
[9]
Bcl-2 down-regulation is a novel mechanism of paclitaxel resistance [J].
Ferlini, C ;
Raspaglio, G ;
Mozzetti, S ;
Distefano, M ;
Filippetti, F ;
Martinelli, E ;
Ferrandina, G ;
Gallo, D ;
Ranelletti, FO ;
Scambia, G .
MOLECULAR PHARMACOLOGY, 2003, 64 (01) :51-58
[10]
Paclitaxel Directly Binds to Bcl-2 and Functionally Mimics Activity of Nur77 [J].
Ferlini, Cristiano ;
Cicchillitti, Lucia ;
Raspaglio, Giuseppina ;
Bartollino, Silvia ;
Cimitan, Samanta ;
Bertucci, Carlo ;
Mozzetti, Simona ;
Gallo, Daniela ;
Persico, Marco ;
Fattorusso, Caterina ;
Campiani, Giuseppe ;
Scambia, Giovanni .
CANCER RESEARCH, 2009, 69 (17) :6906-6914