Three-dimensional structure of the apoptosome: Implications for assembly, procaspase-9 binding, and activation

被引:652
作者
Acehan, D
Jiang, XJ
Morgan, DG
Heuser, JE
Wang, XD
Akey, CW
机构
[1] Boston Univ, Sch Med, Dept Physiol & Biophys, Boston, MA 02118 USA
[2] Univ Texas, SW Med Ctr, Dept Biochem, Dallas, TX 75235 USA
[3] Univ Texas, SW Med Ctr, Howard Hughes Med Inst, Dallas, TX 75235 USA
[4] Harvard Univ, Sch Med, Howard Hughes Med Inst, Boston, MA 02115 USA
[5] Harvard Univ, Sch Med, Dept Cell Biol, Boston, MA 02115 USA
[6] Washington Univ, Sch Med, Dept Cell Biol, St Louis, MO 63110 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/S1097-2765(02)00442-2
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
The apoptosome is an Apaf-1 cytochrome c complex that activates procaspase-9. The three-dimensional structure of the apoptosome has been determined at 27 Angstrom resolution, to reveal a wheel-like particle with 7-fold symmetry. Molecular modeling was used to identify the caspase recruitment and WD40 domains within the apoptosome and to infer likely positions of the CED4 homology motif and cytochrome c. This analysis suggests a plausible role for cytochrome c in apoptosome assembly. In a subsequent structure, a noncleavable mutant of procaspase-9 was localized to the central region of the apoptosome. This complex promotes the efficient activation of procaspase-3. Therefore, the cleavage of procaspase-9 is not required to form an active cell death complex.
引用
收藏
页码:423 / 432
页数:10
相关论文
共 36 条
  • [1] The domains of death: evolution of the apoptosis machinery
    Aravind, L
    Dixit, VM
    Koonin, EV
    [J]. TRENDS IN BIOCHEMICAL SCIENCES, 1999, 24 (02) : 47 - 53
  • [2] Biochemical pathways of caspase activation during apoptosis
    Budihardjo, I
    Oliver, H
    Lutter, M
    Luo, X
    Wang, XD
    [J]. ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 1999, 15 : 269 - 290
  • [3] The structure of TolB, an essential component of the tol-dependent translocation system, and its protein-protein interaction with the translocation domain of colicin E9
    Carr, S
    Penfold, CN
    Bamford, V
    James, R
    Hemmings, AM
    [J]. STRUCTURE WITH FOLDING & DESIGN, 2000, 8 (01): : 57 - 66
  • [4] CHAL J, 2001, CELL, V107, P399
  • [5] Mitochondria as the central control point of apoptosis
    Desagher, S
    Martinou, JC
    [J]. TRENDS IN CELL BIOLOGY, 2000, 10 (09) : 369 - 377
  • [6] Insights into programmed cell death through structural biology
    Fesik, SW
    [J]. CELL, 2000, 103 (02) : 273 - 282
  • [7] SPIDER and WEB: Processing and visualization of images in 3D electron microscopy and related fields
    Frank, J
    Radermacher, M
    Penczek, P
    Zhu, J
    Li, YH
    Ladjadj, M
    Leith, A
    [J]. JOURNAL OF STRUCTURAL BIOLOGY, 1996, 116 (01) : 190 - 199
  • [8] Crystal structure at 2.4 angstrom resolution of the complex of transducin beta gamma and its regulator, phosducin
    Gaudet, R
    Bohm, A
    Sigler, PB
    [J]. CELL, 1996, 87 (03) : 577 - 588
  • [9] The coordinate release of cytochrome c during apoptosis is rapid, complete and kinetically invariant
    Goldstein, JC
    Waterhouse, NJ
    Juin, P
    Evan, GI
    Green, DR
    [J]. NATURE CELL BIOLOGY, 2000, 2 (03) : 156 - 162
  • [10] PROTOCOL FOR 3-D VISUALIZATION OF MOLECULES ON MICA VIA THE QUICK-FREEZE, DEEP-ETCH TECHNIQUE
    HEUSER, J
    [J]. JOURNAL OF ELECTRON MICROSCOPY TECHNIQUE, 1989, 13 (03): : 244 - 263