4.6 Review

Emerging challenges in the design of selective substrates, inhibitors and activity-based probes for indistinguishable proteases

Journal

FEBS JOURNAL
Volume 284, Issue 10, Pages 1518-1539

Publisher

WILEY
DOI: 10.1111/febs.14001

Keywords

activity-based probe; endopeptidase; exopeptidase; protease; substrate specificity

Funding

  1. Polish National Center of Science [2014/13/B/ST5/00240, 2014/14/M/ST5/00619, 2013/11/N/ST5/01995]
  2. European Union [661187]
  3. Foundation for Polish Science
  4. Marie Curie Actions (MSCA) [661187] Funding Source: Marie Curie Actions (MSCA)

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Proteases are enzymes that hydrolyze the peptide bond of peptide substrates and proteins. Despite significant progress in recent years, one of the greatest challenges in the design and testing of substrates, inhibitors and activity-based probes for proteolytic enzymes is achieving specificity toward only one enzyme. This specificity is particularly important if the enzyme is present with other enzymes with a similar catalytic mechanism and substrate specificity but completely different functionality. The cross-reactivity of substrates, inhibitors and activity-based probes with other enzymes can significantly impair or even prevent investigations of a target protease. In this review, we describe important concepts and the latest challenges, focusing mainly on peptide-based substrate specificity techniques used to distinguish individual enzymes within major protease families.

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