SARS‐CoV‐2 Papain‐Like Protease: Structure, Function and Inhibition
Open Access
- 8 September 2022
- journal article
- review article
- Published by Wiley in ChemBioChem
- Vol. 23 (19) , e202200327
Abstract
Emerging variants of SARS‐CoV‐2 and potential novel epidemic coronaviruses underline the importance of investigating various viral proteins as potential drug targets. The papain‐like protease of coronaviruses has been less explored than other viral proteins; however, its substantive role in viral replication and impact on the host immune response make it a suitable target to study. This review article focuses on the structure and function of the papain‐like protease (PLpro) of SARS‐CoV‐2, including variants of concern, and compares it to those of other coronaviruses, such as SARS‐CoV‐1 and MERS‐CoV. The protease's recognition motif is mirrored in ubiquitin and ISG15, which are involved in the antiviral immune response. Inhibitors, including GRL0617 derivatives, and their prospects as potential future antiviral agents are also discussed.Keywords
Funding Information
- Australian Research Council (DE190100015, DP200100348)
This publication has 95 references indexed in Scilit:
- Genomic Characterization of a Newly Discovered Coronavirus Associated with Acute Respiratory Distress Syndrome in HumansmBio, 2012
- Coronavirus Genomics and Bioinformatics AnalysisViruses, 2010
- Requirements for a lead compound to become a clinical candidateBMC Neuroscience, 2008
- A noncovalent class of papain-like protease/deubiquitinase inhibitors blocks SARS virus replicationProceedings of the National Academy of Sciences, 2008
- Severe acute respiratory syndrome coronavirus papain-like protease: Structure of a viral deubiquitinating enzymeProceedings of the National Academy of Sciences, 2006
- UCSF Chimera—A visualization system for exploratory research and analysisJournal of Computational Chemistry, 2004
- WebLogo: A Sequence Logo Generator: Figure 1Genome Research, 2004
- Characterization of a Novel Coronavirus Associated with Severe Acute Respiratory SyndromeScience, 2003
- Regulatory functions of ubiquitination in the immune systemNature Immunology, 2002
- On the size of the active site in proteases. I. PapainBiochemical and Biophysical Research Communications, 1967