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Protein TAILS: when termini tell tales of proteolysis and function

Journal

CURRENT OPINION IN CHEMICAL BIOLOGY
Volume 17, Issue 1, Pages 73-82

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.cbpa.2012.11.025

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Funding

  1. Canadian Institutes of Health Research
  2. Canadian Breast Cancer Research Alliance
  3. Canadian Breast Cancer Foundation
  4. Cancer Research Society
  5. Canada Research Chair
  6. Michael Smith Foundation for Health Research
  7. Breast Cancer Society of Canada
  8. Alexander von Humboldt Foundation
  9. German Federal Ministry of Education and Research

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Among the hundreds of posttranslational modifications, limited proteolysis, also known as processing, is special: It is irreversible, near ubiquitous, and by trimming peptide chains from their ends or cutting proteins into two, proteolysis forms shorter chains displaying new termini. The unique chemistry and location of a-amino-termini and carboxyl-termini in a protein engender special chemical and physical properties to a protein. Hence, modification of protein termini is often associated with new biological activities of a protein. We highlight recent proteomic developments enabling high throughput identification of protein termini. This has revolutionized degradomics and protein characterization by mapping the specificity of terminal modifications and of proteases, and has been used to directly identify new protease substrates and molecular pathways altered by proteolysis.

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