Sequence and functional similarities between pro-apoptotic Bid and plant lipid transfer proteins

被引:27
作者
Esposti, MD [1 ]
机构
[1] Univ Manchester, Sch Biol Sci, Canc Res Campaign, Mol Pharmacol Grp, Manchester M13 9PT, Lancs, England
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS | 2002年 / 1553卷 / 03期
关键词
mitochondria; apoptosis; Bid; Bcl-2; Nix; protein sequence similarity; lipid transfer; cytochrome c;
D O I
10.1016/S0005-2728(02)00187-1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Pro-apoptotic proteins of the Bcl-2 family are known to act on mitochondria and facilitate the release of cytochrome c, but the biochemical mechanism of this action is unknown. Association with mitochondrial membranes is likely to be important in determining the capacity of releasing cytochrome c. The present work provides new evidence suggesting that some pro-apoptotic proteins like Bid have an intrinsic capacity of binding and exchanging membrane lipids. Detailed analysis indicates a significant sequence similarity, between a subset of Bcl-2 family proteins including Bid and Nix and plant lipid transfer proteins. The similar structural signatures could be related to common interactions with membrane lipids. Indeed, isolated Bid shows a lipid transfer activity that is even higher than that of plant lipid transfer proteins. To investigate the possible relevance of these structure-function correlations to the apoptotic action of Bid. cell free assays were established with isolated mitochondria. recombinant Bid and a variety of exogenous lipids. Micromolar concentrations of lysolipids such as lysophosphatidylcholine were found to change the association of Bid with mitochondria and also stimulate the release of cytochrome c promoted by Bid. The changes in mitochondrial association and cytochrome c release were enhanced by the presence of liposomes of lipid composition similar to that of mitochondrial membranes. Thus. a mixture of liposomes, mitochondria and key lysolipids could reproduce the conditions enabling Bid to transfer lipids between donor and acceptor membranes. and also change its reversible association with mitochondria. Bid was also found to enhance the incorporation of a fluorescent lysolipid. but not of a related fatty acid. into mitochondria. On the basis of the results presented here. it is hypothesised that Bid action may depend upon its capacity of exchanging lipids and lysolipids with mitochondrial membranes. The hypothesis is discussed in relation to current models for the integrated action of pro-apoptotic proteins of the Bcl-2 family. (C), 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:331 / 340
页数:10
相关论文
共 51 条
[1]   The Bcl-2 protein family: Arbiters of cell survival [J].
Adams, JM ;
Cory, S .
SCIENCE, 1998, 281 (5381) :1322-1326
[2]   Gapped BLAST and PSI-BLAST: a new generation of protein database search programs [J].
Altschul, SF ;
Madden, TL ;
Schaffer, AA ;
Zhang, JH ;
Zhang, Z ;
Miller, W ;
Lipman, DJ .
NUCLEIC ACIDS RESEARCH, 1997, 25 (17) :3389-3402
[3]   A trace amount of the human pro-apoptotic factor bax induces bacterial death accompanied by damage of DNA [J].
Asoh, S ;
Nishimaki, K ;
Nanbu-Wakao, R ;
Ohta, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (18) :11384-11391
[4]   Bax, but not Bcl-xL, decreases the lifetime of planar phospholipid bilayer membranes at subnanomolar concentrations [J].
Basañez, G ;
Nechushtan, A ;
Drozhinin, O ;
Chanturiya, A ;
Choe, E ;
Tutt, S ;
Wood, KA ;
Hsu, YT ;
Zimmerberg, J ;
Youle, RJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (10) :5492-5497
[5]   Leber's hereditary optic neuropathy: Biochemical effect of 11778/ND4 and 3460/ND1 mutations and correlation with the mitochondrial genotype [J].
Carelli, V ;
Ghelli, A ;
Ratta, M ;
Bacchilega, E ;
Sangiorgi, S ;
Mancini, R ;
Leuzzi, V ;
Cortelli, P ;
Montagna, P ;
Lugaresi, E ;
Esposti, MD .
NEUROLOGY, 1997, 48 (06) :1623-1632
[6]   BCL-2 FAMILY: Regulators of cell death [J].
Chao, DT ;
Korsmeyer, SJ .
ANNUAL REVIEW OF IMMUNOLOGY, 1998, 16 :395-419
[7]   Nix and Nip3 form a subfamily of pro-apoptotic mitochondrial proteins [J].
Chen, G ;
Cizeau, J ;
Velde, CV ;
Park, JH ;
Bozek, G ;
Bolton, J ;
Shi, L ;
Dubik, D ;
Greenberg, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (01) :7-10
[8]   BCL-2, BCL-XL sequester BH3 domain-only molecules preventing BAX- and BAK-mediated mitochondrial apoptosis [J].
Cheng, EHYA ;
Wei, MC ;
Weiler, S ;
Flavell, RA ;
Mak, TW ;
Lindsten, T ;
Korsmeyer, SJ .
MOLECULAR CELL, 2001, 8 (03) :705-711
[9]   A CONSERVED DOMAIN IN BAK, DISTINCT FROM BH1 AND BH2, MEDIATES CELL-DEATH AND PROTEIN-BINDING FUNCTIONS [J].
CHITTENDEN, T ;
FLEMINGTON, C ;
HOUGHTON, AB ;
EBB, RG ;
GALLO, GJ ;
ELANGOVAN, B ;
CHINNADURAI, G ;
LUTZ, RJ .
EMBO JOURNAL, 1995, 14 (22) :5589-5596
[10]   Solution structure of BID, an intracellular amplifier of apoptotic signaling [J].
Chou, JJ ;
Li, HL ;
Salvesen, GS ;
Yuan, JY ;
Wagner, G .
CELL, 1999, 96 (05) :615-624