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公开(公告)号:US20060003939A1
公开(公告)日:2006-01-05
申请号:US10431638
申请日:2003-05-08
申请人: Hermann Steller , Hyung Ryoo , Aaron Ciechanover , Hedva Gonen
发明人: Hermann Steller , Hyung Ryoo , Aaron Ciechanover , Hedva Gonen
CPC分类号: C07K14/4747 , A61K38/00 , C07K7/06 , C07K7/08 , C12N2799/026
摘要: The present invention provides novel peptides, nucleic acids, compounds, compositions and methods for regulating apoptosis, and screening methods for identifying same. Regulation of apoptosis is mediated via IAPi-derived proteins, peptide fragments thereof, and nucleic acids encoding same, stimulating/accelerating or downmodulating/suppressing apoptosis. For stimulation/acceleration of apoptosis, the IAPi-derived proteins or peptide fragments thereof comprise RHG and Trp-box amino acid consensus sequences. Stimulation/acceleration results in self-ubiquitination and auto-degradation of an IAP. For downmodulation/suppression of apoptosis, IAPi-derived proteins or peptide fragments thereof comprising either RHG or Trp-box amino acid consensus sequences, or both, failing to stimulate or suppressing self-ubiquitination and auto-degradation of an IAP, result in suppression of apoptosis.
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公开(公告)号:US20060058229A1
公开(公告)日:2006-03-16
申请号:US10513465
申请日:2003-05-08
申请人: Hermann Steller , Hyung Ryoo , Aaron Ciechanover , Hedva Gonen
发明人: Hermann Steller , Hyung Ryoo , Aaron Ciechanover , Hedva Gonen
IPC分类号: A61K38/17
CPC分类号: C07K14/4747 , A61K38/00
摘要: The present invention provides novel peptides, nucleic acids, compounds, compositions and methods for regulating apoptosis, and screening methods for identifying same. Regulation of apoptosis is mediated via IAPi-derived proteins, peptide fragments thereof, and nucleic acids encoding same, stimulating/accelerating or downmodulating/suppressing apoptosis. For stimulation/acceleration of apoptosis, the IAPi-derived proteins or peptide fragments thereof comprise RHG and Trp-box amino acid consensus sequences. Stimulation/acceleration results in self-ubiquitination and auto-degradation of an IAP. For downmodulation/suppression of apoptosis, IAPi-derived proteins or peptide fragments thereof comprising either RHG or Trp-box amino acid consensus sequences, or both, failing to stimulate or suppressing self-ubiquitination and auto-degradation of an IAP, result in suppression of apoptosis.
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