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Metalloprotoporphyrin Inhibition of HCV NS3-4A Protease: Structure–Activity Relationships
- Source :
- Drug Design, Development and Therapy
- Publication Year :
- 2020
- Publisher :
- Dove, 2020.
-
Abstract
- Background Antiviral actions of tetrapyrroles have been described in a number of systems. Our goal was to evaluate antagonism of the HCV NS3-4A protease by a variety of common porphyrins and characterize structure–activity relationships that may be useful for future drug design of HCV and related Flaviviruses. Methods Using fluorometric assays, common metalloprotoporphyrins (MPP) all inhibited NS3-4A protease with IC50 values in low micromolar ranges [CoPP (1.4 µM) < ZnPP = MnPP = SnPP < CuPP < FePP (6.5 µM) = protoporphyrin]. Results Lineweaver–Burk plots confirmed that MPP: NS3 inhibition was basically competitive. All tested MPPs inhibited HCV genotype 1A, 1B, 2A and 3A recombinant proteases with the same fidelity suggesting wide antagonistic capabilities. However, when the MPPs were tested in cellular incubations with HCV replicons only Zn, Fe and free-base protoporphyrin showed comparable EC50 and IC50 values suggesting that there may be critical differences in MPP uptake and intracellular availability. Meso, deutero, and isohematoporphyrin derivatives, with or without metal substitution, all showed less anti-protease and antiviral activities as compared to protoporphyrins, suggesting that the planar, vinyl side chains are important for protease active site binding. MPPs were also active against three common protease mutants (T54A, A156T, and V36M) with equivalent or better IC50 values as compared to wild type enzyme. Conclusion These findings document the versatility of MPPs as antiviral agents with an expanded sensitivity for HCV genotypes and resistance to some common viral mutations. The results also suggest that further study of MPP structure and function will be useful for the development of new antiviral agents.
- Subjects :
- hepatitis C virus
Dose-Response Relationship, Drug
Molecular Structure
Hepacivirus
Microbial Sensitivity Tests
Viral Nonstructural Proteins
porphyrins
Virus Replication
Antiviral Agents
Structure-Activity Relationship
Humans
Protease Inhibitors
Serine Proteases
hepatitis C genotype
Cells, Cultured
Original Research
Subjects
Details
- Language :
- English
- ISSN :
- 11778881
- Volume :
- 14
- Database :
- OpenAIRE
- Journal :
- Drug Design, Development and Therapy
- Accession number :
- edsair.pmid..........06475bf69fd056551d52923d4b603389