4.3 Review

Serine Hydrolase Activity-Based Probes for use in Chemical Proteomics

Journal

ISRAEL JOURNAL OF CHEMISTRY
Volume 63, Issue 3-4, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ijch.202300016

Keywords

serine hydrolase; activity-based protein profiling; activity-based probes; serine hydrolase inhibitors; imaging

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Protein profiling and probe development in the field of serine hydrolases are crucial for studying biological processes. The use of activity-based protein profiling and probes has expanded our understanding of the SH proteome and led to the development of selective inhibitors and imaging agents with broad applications.
Serine hydrolases (SHs) comprise a large superfamily of enzymes that play critical roles in many biological processes. Despite their importance, many SHs remain uncharacterized and the vast majority of SHs lack selective inhibitors. In response, activity-based protein profiling (ABPP) and activity-based probes (ABPs) have been leveraged to construct a more comprehensive picture of the SH proteome. Since the utility of ABPP is largely dictated by the reactivity profile of the ABPs deployed, novel scaffolds and chemotypes are needed to expand the breadth and selectivity of SH-targeting ABPs. In this review, we highlight recent innovations in SH probe development, covering both established and emerging electrophilic warheads. We then discuss how strategic implementation of SH-targeting ABPs has yielded selective, potent inhibitors and imaging agents with broad use. Finally, we present methods for ABP diversification and explore cutting-edge applications in therapeutics development and discovery biology.

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