Cited by 330Protease and Inhibitor MechanismsBlood Coagulation and Thrombosis MechanismsUbiquitin and proteasome pathways

Activity-Based Profiling of Proteases

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Sanman, Laura E., Bogyo, Matthew·2014·Annual Review of Biochemistry

Abstract

Proteolytic enzymes are key signaling molecules in both normal physiological processes and various diseases. After synthesis, protease activity is tightly controlled. Consequently, levels of protease messenger RNA and protein often are not good indicators of total protease activity. To more accurately assign function to new proteases, investigators require methods that can be used to detect and quantify proteolysis. In this review, we describe basic principles, recent advances, and applications of biochemical methods to track protease activity, with an emphasis on the use of activity-based probes (ABPs) to detect protease activity. We describe ABP design principles and use case studies to illustrate the application of ABPs to protease enzymology, discovery and development of protease-targeted drugs, and detection and validation of proteases as biomarkers.

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Crossref · 10.1146/annurev-biochem-060713-035352

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  • Some analytical techniques (click chemistry, activity probes, and mass spectrometry-based proteomics) to evaluate binding activity and selectivity in vitro and in vivo are only available for covalent compounds.

    “In addition, some analytical techniques such as click chemistry, activity probes, and mass spectrometry-based proteomics to evaluate binding activity and selectivity in vitro and in vivo are only available for covalent compounds [120–124].”

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References 125 · Cited by 330

Research works printed but not linked: 1

  1. Jessani N, Liu Y, Humphrey M, Cravatt BF. 2002. Enzyme activity profiles of the secreted and membrane proteome that depict cancer cell invasiveness. Proc. Natl. Acad. Sci. USA 99:10335-40 120.

Authors
Sanman, L. E., & Bogyo, M.
Affiliations
  • Departments of 1Chemical and Systems Biology,
  • Stanford Medicine (US)
Venue
Annual Review of Biochemistry
Published
2014-06-02
Volume
83
Issue
1
Pages
249-273
ISSN
  • 0066-4154 (ISSN-L)
  • 1545-4509
OpenAlex
W2159000061
Cited by
330
References
125
Citations by year
2026: 15 · 2025: 22 · 2024: 17 · 2023: 31 · 2022: 31 · 2021: 27 · 2020: 33 · 2019: 40 · 2018: 24 · 2017: 34 · 2016: 28 · 2015: 26 · 2014: 2
FWCI
3.03
Type
journal article
Language
en
Open access
Locations
  • Annual Review of Biochemistry (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • National Science Foundation
  • National Institutes of Health (DGE-114747)
  • National Institute of Biomedical Imaging and Bioengineering (R01EB005011)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Protease and Inhibitor Mechanisms
  • Health Sciences › Medicine › Hematology › Blood Coagulation and Thrombosis Mechanisms
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ubiquitin and proteasome pathways
Keywords
proteolytic enzymes, activity-based probes, protease activity detection
MeSH terms
Animals, Biochemistry, Chemistry, Pharmaceutical, Escherichia coli, Humans, Peptide Hydrolases, Peptides, Substrate Specificity, Drug Design, Biomarkers, Caspases, Proteomics

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