Literature DB >> 14993223

Pro-apoptotic proteins released from the mitochondria regulate the protein composition and caspase-processing activity of the native Apaf-1/caspase-9 apoptosome complex.

Davina Twiddy1, David G Brown, Colin Adrain, Rebekah Jukes, Seamus J Martin, Gerald M Cohen, Marion MacFarlane, Kelvin Cain.   

Abstract

The apoptosome is a large caspase-activating ( approximately 700-1400 kDa) complex, which is assembled from Apaf-1 and caspase-9 when cytochrome c is released during mitochondrial-dependent apoptotic cell death. Apaf-1 the core scaffold protein is approximately 135 kDa and contains CARD (caspase recruitment domain), CED-4, and multiple (13) WD40 repeat domains, which can potentially interact with a variety of unknown regulatory proteins. To identify such proteins we activated THP.1 lysates with dATP/cytochrome c and used sucrose density centrifugation and affinity-based methods to purify the apoptosome for analysis by MALDI-TOF mass spectrometry. First, we used a glutathione S-transferase (GST) fusion protein (GST-casp9(1-130)) containing the CARD domain of caspase-9-(1-130), which binds to the CARD domain of Apaf-1 when it is in the apoptosome and blocks recruitment/activation of caspase-9. This affinity-purified apoptosome complex contained only Apaf-1XL and GST-casp9(1-130), demonstrating that the WD40 and CED-4 domains of Apaf-1 do not stably bind other cytosolic proteins. Next we used a monoclonal antibody to caspase-9 to immunopurify the native active apoptosome complex from cell lysates, containing negligible levels of cytochrome c, second mitochondria-derived activator of caspase (Smac), or Omi/HtrA2. This apoptosome complex exhibited low caspase-processing activity and contained four stably associated proteins, namely Apaf-1, pro-p35/34 forms of caspase-9, pro-p20 forms of caspase-3, X-linked inhibitor of apoptosis (XIAP), and cytochrome c, which was only bound transiently to the complex. However, in lysates containing Smac and Omi/HtrA2, the caspase-processing activity of the purified apoptosome complex increased 6-8-fold and contained only Apaf-1 and the p35/p34-processed subunits of caspase-9. During apoptosis, Smac, Omi/HtrA2, and cytochrome c are released simultaneously from mitochondria, and thus it is likely that the functional apoptosome complex in apoptotic cells consists primarily of Apaf-1 and processed caspase-9.

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Year:  2004        PMID: 14993223     DOI: 10.1074/jbc.M311388200

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  22 in total

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Review 2.  Cell death controlling complexes and their potential therapeutic role.

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3.  A systems biology analysis of apoptosome formation and apoptosis execution supports allosteric procaspase-9 activation.

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Journal:  J Biol Chem       Date:  2014-08-08       Impact factor: 5.157

4.  The E3 ligase PARC mediates the degradation of cytosolic cytochrome c to promote survival in neurons and cancer cells.

Authors:  Vivian Gama; Vijay Swahari; Johanna Schafer; Adam J Kole; Allyson Evans; Yolanda Huang; Anna Cliffe; Brian Golitz; Noah Sciaky; Xin-Hai Pei; Yue Xiong; Mohanish Deshmukh
Journal:  Sci Signal       Date:  2014-07-15       Impact factor: 8.192

5.  PI3K/Akt pathway involving into apoptosis and invasion in human colon cancer cells LoVo.

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6.  Role of cytochrome C in apoptosis: increased sensitivity to tumor necrosis factor alpha is associated with respiratory defects but not with lack of cytochrome C release.

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7.  Systems analysis of cancer cell heterogeneity in caspase-dependent apoptosis subsequent to mitochondrial outer membrane permeabilization.

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8.  Clinical and experimental study of oxaliplatin in treating human gastric carcinoma.

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Journal:  World J Gastroenterol       Date:  2004-10-01       Impact factor: 5.742

9.  Cardiolipin modulates allosterically the nitrite reductase activity of horse heart cytochrome c.

Authors:  Paolo Ascenzi; Maria Marino; Fabio Polticelli; Roberto Santucci; Massimo Coletta
Journal:  J Biol Inorg Chem       Date:  2014-06-27       Impact factor: 3.358

10.  Sub-millimolar concentration of the novel phenol-based compound, 2-hydroxy benzoate zinc, induces apoptosis in human HT-1080 fibrosarcoma cells.

Authors:  J G Mahdi; C J Pepper; M A Alkarrawi; A J Mahdi; I D Bowen
Journal:  Cell Prolif       Date:  2009-11-17       Impact factor: 6.831

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