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Protease research in the era of systems biology

  • Ulrich auf dem Keller , Alain Doucet and Christopher M. Overall
Published/Copyright: November 2, 2007
Biological Chemistry
From the journal Volume 388 Issue 11

Abstract

Proteases are specific modulators of signaling molecules and their underlying pathways in addition to their degradative roles. However, proteases do not act alone, but form cascades, circuits and networks that all dynamically interconnect to form the protease web, which defines the proteolytic potential of a cell or tissue in a defined condition. To describe the protease web and its net activity several novel high-throughput proteomic techniques, in the field termed degradomics, have been developed. Emerging systems biology methods to evaluate the expression, activity and substrate discovery of proteases are presented. Understanding the protease web and its perturbations in pathology will help to develop new therapeutics for the treatment of diseases, such as cancer, arthritis and chronic obstructive pulmonary diseases.


Corresponding author

Published Online: 2007-11-02
Published in Print: 2007-11-01

©2007 by Walter de Gruyter Berlin New York

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  3. Cysteine cathepsin non-inhibitory binding partners: modulating intracellular trafficking and function
  4. Cysteine proteases: destruction ability versus immunomodulation capacity in immune cells
  5. ‘Species’ of peptidases
  6. Protease research in the era of systems biology
  7. Human and mouse homo-oligomeric meprin A metalloendopeptidase: substrate and inhibitor specificities
  8. Association of cathepsin E with tumor growth arrest through angiogenesis inhibition and enhanced immune responses
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  10. Cellular localization of MAGI-1 caspase cleavage products and their role in apoptosis
  11. Differential methylation kinetics of individual target site strands by T4Dam DNA methyltransferase
  12. Characterisation of zinc-binding domains of peroxisomal RING finger proteins using size exclusion chromatography/inductively coupled plasma-mass spectrometry
  13. Defining the extended substrate specificity of kallikrein 1-related peptidases
  14. Latent MMP-9 is bound to TIMP-1 before secretion
  15. Novel expression of kallikreins, kallikrein-related peptidases and kinin receptors in human pleural mesothelioma
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  17. Clinical chemistry reference database for Wistar rats and C57/BL6 mice
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