ABSTRACT
Introduction
Ubiquitin specific peptidase 30 (USP30) is a mitochondrial deubiquitinase that antagonizes ubiquitination-mediated mitophagy of damaged or impaired mitochondria driven by the activity of PARK2/Parkin ubiquitin ligase and PINK1 protein kinase. Researchers have related low levels of USP30 to enhanced mitophagy and therefore have been pursuing mitophagy activation utilizing USP30 inhibitors as an alternative approach to target neurodegenerative disorders and other human diseases associated with defective mitophagy.
Areas covered
This review covers the research and patent literature on the discovery and development of USP30 inhibitors since 2013.
Expert opinion
Strategies toward mitophagy activation utilizing small-molecule inhibitors of USP30 have emerged as alternative pathways for the potential treatment of many human diseases. Research efforts have led to identifying potent and selective small-molecule USP30 inhibitors. Most small-molecule USP30 inhibitors share a common N-cyano motif that binds covalently to the target. Non-covalently binding inhibitors have recently been disclosed as well. Lead compounds exhibit satisfactory inhibitory activities and are currently in preclinical development. Regrettably, complete pharmacological characterization and in vivo evaluation to validate and prove the therapeutic potential is lacking. Target validation could pave the way for discovering and developing USP30 inhibitors that could ultimately lead to marketed drugs.
Acknowledgments
The authors would like to thank Professor Shuya Fukai from Department of Chemistry, Graduate School of Science, Kyoto University, Kyoto, Japan and Dr Yusuke Sato from the Center for Research on Green Sustainable Chemistry, Department of Engineering, Tottori University, Tottori, Japan, for their excellent assistance in providing the re-worked, high-quality pictures of the overall crystal structures and the detailed views of the USP30-Lys6 linked diubiquitin complex, and their permission to use these.
Declaration of interests
The author(s) are employees of Janssen Pharmaceutica NV. The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript apart from those disclosed.
Reviewer disclosures
Peer reviewers on this manuscript have no relevant financial or other relationships to disclose.