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Specific ligands for classical swine fever virus screened from landscape phage display library.
- Source :
-
Antiviral research [Antiviral Res] 2014 Sep; Vol. 109, pp. 68-71. Date of Electronic Publication: 2014 Jun 28. - Publication Year :
- 2014
-
Abstract
- Classical swine fever (CSF) is a devastating infectious disease caused by classical swine fever virus (CSFV). The screening of CSFV-specific ligands is of great significance for diagnosis and treatment of CSF. Affinity selection from random peptide libraries is an efficient approach to discover ligands with high stability and specificity. Here, we screened phage ligands for the CSFV E2 protein from f8/8 landscape phage display library by biopanning and obtained four phage clones specific for the E2 protein of CSFV. Viral blocking assays indicated that the phage clone displaying the octapeptide sequence DRATSSNA remarkably inhibited the CSFV replication in PK-15 cells at a titer of 10(10) transduction units, as evidenced by significantly decreased viral RNA copies and viral titers. The phage-displayed E2-binding peptides have the potential to be developed as antivirals for CSF.<br /> (Copyright © 2014 Elsevier B.V. All rights reserved.)
- Subjects :
- Amino Acid Sequence
Animals
Antiviral Agents chemistry
Antiviral Agents metabolism
Bacteriophages genetics
Bacteriophages metabolism
Classical Swine Fever virology
Classical Swine Fever Virus genetics
Classical Swine Fever Virus physiology
Drug Evaluation, Preclinical
Ligands
Molecular Sequence Data
Peptides chemistry
Peptides genetics
Peptides metabolism
Protein Binding
Swine
Viral Envelope Proteins genetics
Viral Envelope Proteins metabolism
Virus Replication drug effects
Antiviral Agents pharmacology
Classical Swine Fever Virus drug effects
Peptide Library
Peptides pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1872-9096
- Volume :
- 109
- Database :
- MEDLINE
- Journal :
- Antiviral research
- Publication Type :
- Academic Journal
- Accession number :
- 24977927
- Full Text :
- https://doi.org/10.1016/j.antiviral.2014.06.012