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Novel highly selective inhibitors of ubiquitin specific protease 30 (USP30) accelerate mitophagy
- Source :
- Bioorganicmedicinal chemistry letters. 28(15)
- Publication Year :
- 2018
-
Abstract
- Mitophagy is one of the processes that cells use to maintain overall health. An E3 ligase, parkin, ubiquitinates mitochondrial proteins prior to their degradation by autophagasomes. USP30 is an enzyme that de-ubiquitinates mitochondrial proteins; therefore, inhibiting this enzyme could foster mitophagy. Herein, we disclose the structure-activity relationships (SAR) within a novel series of highly selective USP30 inhibitors. Two structurally similar compounds, MF-094 (a potent and selective USP30 inhibitor) and MF-095 (a significantly less potent USP30 inhibitor), serve as useful controls for biological evaluation. We show that MF-094 increases protein ubiquitination and accelerates mitophagy.
- Subjects :
- 0301 basic medicine
Ubiquitin-Protein Ligases
Clinical Biochemistry
Pharmaceutical Science
Biochemistry
Parkin
Mitochondrial Proteins
03 medical and health sciences
Mice
Structure-Activity Relationship
Drug Discovery
Mitophagy
Ubiquitin specific protease
Animals
Protease Inhibitors
Molecular Biology
Mitochondrial protein
chemistry.chemical_classification
biology
Chemistry
Organic Chemistry
Ubiquitination
Highly selective
Protein ubiquitination
Ubiquitin ligase
Cell biology
Mitochondria
030104 developmental biology
Enzyme
biology.protein
Molecular Medicine
Thiolester Hydrolases
Subjects
Details
- ISSN :
- 14643405
- Volume :
- 28
- Issue :
- 15
- Database :
- OpenAIRE
- Journal :
- Bioorganicmedicinal chemistry letters
- Accession number :
- edsair.doi.dedup.....5b97527aa8a23c2e86ce12f953f1aa4a