Proteases are important targets for the treatment of human disease. Several protease inhibitors have failed in clinical trials due to a lack of in vivo specificity, indicating the need for studies of protease function and inhibition in complex, disease-related models. The tight post-translational regulation of protease activity complicates protease analysis by traditional proteomics methods. Activity-based protein profiling is a powerful technique that can resolve this issue. It uses small-molecule tools-activity-based probes-to label and analyze active enzymes in lysates, cells, and whole animals. Over the last twelve years, a wide variety of protease activity-based probes have been developed. These synthetic efforts have enabled techniques ranging from real-time in vivo imaging of protease activity to high-throughput screening of uncharacterized proteases. This Review introduces the general principles of activity-based protein profiling and describes the recent advancements in probe design and analysis techniques, which have increased the knowledge of protease biology and will aid future protease drug discovery.
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http://dx.doi.org/10.1002/cmdc.201200057 | DOI Listing |
Chembiochem
March 2025
Colorado School of Mines, Chemistry, 1500 Illinois St, 80403, Golden, UNITED STATES OF AMERICA.
We present the synthesis, properties, and imaging applications of a new class of diazaborine-based probes (Peroxynitrite Probe-1, PNP-1) for selective peroxynitrite (ONOO-) imaging in live cells. PNP-1 features a diazaborine-based reaction motif that provides excellent discrimination between H2O2 and ONOO-, solving a persistent challenge of organoboron-based fluorescent probes for oxidative metabolite imaging. We demonstrate the utility of PNP-1 to detect endogenously produced ONOO- in live RAW 264.
View Article and Find Full Text PDFAnal Chim Acta
April 2025
Faculty of Materials Science and Chemistry, China University of Geosciences, Wuhan, 430074, PR China; State Key Laboratory of Biogeology and Environmental Geology, China University of Geosciences, Wuhan, 430074, PR China.
Background: Methyl parathion, a potent organophosphorus insecticide, is extensively employed in agriculture and animal husbandry, leading to significant environmental contamination with pesticide residues, posing a grave threat to human health. This compound irreversibly inhibits acetylcholinesterase (AChE) in the human nervous system, resulting in the accumulation of acetylcholine (ACh), which is detrimental. Various enzyme activity-based assays have been explored due to its pathogenic mechanism, yet these methods are fraught with limitations.
View Article and Find Full Text PDFAnal Chim Acta
April 2025
School of Life Science and Technology, Wuhan Polytechnic University, Wuhan, 430023, China. Electronic address:
Background: UDG (Uracil-DNA glycosylase) is a pivotal enzyme in the base excision repair (BER) mechanism, and it is widely distributed across most organisms. Its primary function is to identify and excise uracil bases from DNA, thereby facilitating the repair of DNA and the creation of apurinic/apyrimidinic (AP) sites. Furthermore, abnormal expression or dysregulation of UDG activity has been closely associated with ageing, cancer, and other diseases such as immunodeficiency and lymphoma.
View Article and Find Full Text PDFCell Chem Biol
February 2025
Department of Chemistry, The University of Chicago, Chicago, IL 60637, USA; Chan Zuckerberg Biohub, Chicago, IL 60642, USA. Electronic address:
Peroxiredoxins (PRDXs) are a highly conserved family of peroxidases that serve as the primary scavengers of peroxides. Post-translational modifications play crucial roles modulating PRDX activities, tuning the balance between reactive oxygen species (ROS) signaling and stress. We previously reported that S-acylation occurs at the "peroxidatic" cysteine (Cp) site of PRDX5 and that it inhibits PRDX5 activity.
View Article and Find Full Text PDFJ Am Chem Soc
March 2025
Leiden Institute of Chemistry, Leiden University, 2300 RA Leiden, The Netherlands.
During infection, the human opportunistic pathogen Pseudomonas aeruginosa forms protective biofilms, whose matrix consists of proteins, nucleic acids, and polysaccharides such as alginate, Psl, and Pel. Psl, a polymeric pentasaccharide composed of mannose, rhamnose, and glucose, is produced during the early stages of biofilm formation, serving as a protective barrier against antibiotics and the immune system. The Psl biosynthesis gene cluster, besides encoding various glycosyltransferases, also includes an endoglycosidase, PslG.
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