| Literature DB >> 32022538 |
Simon J Mountford1, Bethany M Anderson2,3, Bangyan Xu2, Elean S V Tay2, Monika Szabo1, My-Linh Hoang1, Jiayin Diao3, Luigi Aurelio1, Rhiannon I Campden4, Erik Lindström5, Erica K Sloan3, Robin M Yates4, Nigel W Bunnett3,6,7, Philip E Thompson1, Laura E Edgington-Mitchell2,3,8.
Abstract
Cathepsin X/Z/P is cysteine cathepsin with unique carboxypeptidase activity. Its expression is associated with cancer and neurodegenerative diseases, although its roles during normal physiology are still poorly understood. Advances in our understanding of its function have been hindered by a lack of available tools that can specifically measure the proteolytic activity of cathepsin X. We present a series of activity-based probes that incorporate a sulfoxonium ylide warhead, which exhibit improved specificity for cathepsin X compared to previously reported probes. We apply these probes to detect cathepsin X activity in cell and tissue lysates, in live cells and in vivo, and to localize active cathepsin X in mouse tissues by microscopy. Finally, we utilize an improved method to generate chloromethylketones, necessary intermediates for synthesis of acyloxymethylketones probes, by way of sulfoxonium ylide intermediates. In conclusion, the probes presented in this study will be valuable for investigating cathepsin X pathophysiology.Entities:
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Year: 2020 PMID: 32022538 PMCID: PMC8771941 DOI: 10.1021/acschembio.9b00961
Source DB: PubMed Journal: ACS Chem Biol ISSN: 1554-8929 Impact factor: 5.100