Abstract
Cystatin C is a human cysteine proteinase inhibitor present in extracellular fluids. Cystatin C and a tripeptide derivative (Z-LVG-CHN2) that mimics its proteinase-binding center, were tested for possible antiviral activity against herpes simplex virus type 1 (HSV) and poliovirus type 1. Both recombinant cystatin C and Z-LVG-CHN2 displayed strong inhibitory effects on HSV replication, whereas no significant effect on poliovirus replication was seen. The molar concentration of cystatin C that gave total inhibition of HSV replication was lower than that of either Z-LVG-CHN2 or of acyclovir, the drug currently most used against HSV infections. These results suggest that cysteine proteinase inhibitors might play a physiological role as inhibitors of viral replication and that such proteinase inhibitors, or peptide derivatives that mimic their proteinase-binding centers, might be used as antiviral agents.
MeSH Terms
Amino Acid Sequence
Animals
Antiviral Agents/pharmacology
Cell Line
Cerebrospinal Fluid Proteins/pharmacology
Cystatin C
Cystatins/pharmacology
Kinetics
Molecular Sequence Data
Oligopeptides/pharmacology
Simplexvirus/drug effects,growth & development,physiology
Virus Replication/drug effects
Chemicals
Antiviral Agents
CST3 protein, human
Cerebrospinal Fluid Proteins
Cystatin C
Cystatins
Oligopeptides
N-benzyloxycarbonyl-leucyl-valyl-glycine diazomethane
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Björck L
Department of Medical Microbiology, University of Lund, Sweden.
Grubb A
Kjellén L
References (13)
13 references, click to expand
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