X-ray and NMR structure of human Bcl-xL, an inhibitor of programmed cell death - PubMed (original) (raw)
. 1996 May 23;381(6580):335-41.
doi: 10.1038/381335a0.
M Sattler, H Liang, R P Meadows, J E Harlan, H S Yoon, D Nettesheim, B S Chang, C B Thompson, S L Wong, S L Ng, S W Fesik
Affiliations
- PMID: 8692274
- DOI: 10.1038/381335a0
X-ray and NMR structure of human Bcl-xL, an inhibitor of programmed cell death
S W Muchmore et al. Nature. 1996.
Abstract
THE Bcl-2 family of proteins regulate programmed cell death by an unknown mechanism. Here we describe the crystal and solution structures of a Bcl-2 family member, Bcl-xL (ref. 2). The structures consist of two central, primarily hydrophobic alpha-helices, which are surrounded by amphipathic helices. A 60-residue loop connecting helices alpha1 and alpha2 was found to be flexible and non-essential for anti-apoptotic activity. The three functionally important Bcl-2 homology regions (BH1, BH2 and BH3) are in close spatial proximity and form an elongated hydrophobic cleft that may represent the binding site for other Bcl-2 family members. The arrangement of the alpha-helices in Bcl-xL is reminiscent of the membrane translocation domain of bacterial toxins, in particular diphtheria toxin and the colicins. The structural similarity may provide a clue to the mechanism of action of the Bcl-2 family of proteins.
Similar articles
- Membrane-insertion fragments of Bcl-xL, Bax, and Bid.
García-Sáez AJ, Mingarro I, Pérez-Payá E, Salgado J. García-Sáez AJ, et al. Biochemistry. 2004 Aug 31;43(34):10930-43. doi: 10.1021/bi036044c. Biochemistry. 2004. PMID: 15323553 - A conserved hydrophobic core at Bcl-xL mediates its structural stability and binding affinity with BH3-domain peptide of pro-apoptotic protein.
Feng Y, Zhang L, Hu T, Shen X, Ding J, Chen K, Jiang H, Liu D. Feng Y, et al. Arch Biochem Biophys. 2009 Apr 1;484(1):46-54. doi: 10.1016/j.abb.2009.01.003. Epub 2009 Jan 10. Arch Biochem Biophys. 2009. PMID: 19161970 - Identification of core structural residues in the sequentially diverse and structurally homologous Bcl-2 family of proteins.
Lama D, Sankararamakrishnan R. Lama D, et al. Biochemistry. 2010 Mar 23;49(11):2574-84. doi: 10.1021/bi100029k. Biochemistry. 2010. PMID: 20141168 - Structural biology of the Bcl-2 family of proteins.
Petros AM, Olejniczak ET, Fesik SW. Petros AM, et al. Biochim Biophys Acta. 2004 Mar 1;1644(2-3):83-94. doi: 10.1016/j.bbamcr.2003.08.012. Biochim Biophys Acta. 2004. PMID: 14996493 Review. - Homology Modeling and Docking Studies of Bcl-2 and Bcl-xL with Small Molecule Inhibitors: Identification and Functional Studies.
Salam AAA, Nayek U, Sunil D. Salam AAA, et al. Curr Top Med Chem. 2018;18(31):2633-2663. doi: 10.2174/1568026619666190119144819. Curr Top Med Chem. 2018. PMID: 30659540 Review.
Cited by
- Bcl-xL is translocated to the nucleus via CtBP2 to epigenetically promote metastasis.
Zhang T, Li S, Tan YA, Chen X, Zhang C, Chen Z, Mishra B, Na JH, Choi S, Shin SJ, Damle P, Chougoni KK, Grossman SR, Wang D, Jiang X, Li Y, Hissong E, Chen YT, Xiang JZ, Du YN. Zhang T, et al. Cancer Lett. 2024 Nov 1;604:217240. doi: 10.1016/j.canlet.2024.217240. Epub 2024 Sep 10. Cancer Lett. 2024. PMID: 39265800 - Structure-destabilizing mutations unleash an intrinsic perforation activity of antiapoptotic Bcl-2 in the mitochondrial membrane enabling apoptotic cell death.
Gao P, Zhang Z, Wang R, Huang L, Wu H, Qiao Z, Wang X, Jin H, Peng J, Liu L, Chen Q, Lin J. Gao P, et al. Mitochondrial Commun. 2023;1:48-61. doi: 10.1016/j.mitoco.2023.08.001. Epub 2023 Aug 9. Mitochondrial Commun. 2023. PMID: 39239250 Free PMC article. - Mastering Death: The Roles of Viral Bcl-2 in dsDNA Viruses.
Suraweera CD, Espinoza B, Hinds MG, Kvansakul M. Suraweera CD, et al. Viruses. 2024 May 30;16(6):879. doi: 10.3390/v16060879. Viruses. 2024. PMID: 38932171 Free PMC article. Review. - Underlying Mechanism of Lysosomal Membrane Permeabilization in CNS Injury: A Literature Review.
Xiang L, Lou J, Zhao J, Geng Y, Zhang J, Wu Y, Zhao Y, Tao Z, Li Y, Qi J, Chen J, Yang L, Zhou K. Xiang L, et al. Mol Neurobiol. 2024 Jun 18. doi: 10.1007/s12035-024-04290-6. Online ahead of print. Mol Neurobiol. 2024. PMID: 38888836 Review. - Experimental methods to study the structure and dynamics of intrinsically disordered regions in proteins.
Maiti S, Singh A, Maji T, Saibo NV, De S. Maiti S, et al. Curr Res Struct Biol. 2024 Mar 21;7:100138. doi: 10.1016/j.crstbi.2024.100138. eCollection 2024. Curr Res Struct Biol. 2024. PMID: 38707546 Free PMC article. Review.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases
Research Materials