Utilisation of bacteriophage display libraries to identify peptide sequences recognised by equine herpesvirus type 1 specific equine sera
| Autor: | F. M. Cancellotti, M Marault, Stéphan Zientara, C Cruciere, Matthew M. Binns, Nicholas Davis-Poynter, L. Ceglie, L Taylor, J. A. Mumford, S Ryder, G. Koptopoulos, Duncan Hannant, Ian Birch-Machin, P Iniguez |
|---|---|
| Rok vydání: | 2000 |
| Předmět: |
Phage display
medicine.drug_class Sequence analysis Molecular Sequence Data Enzyme-Linked Immunosorbent Assay Biopanning Biology Monoclonal antibody Antibodies Viral Sensitivity and Specificity Epitope Peptide Library Virology medicine Animals Bacteriophages Amino Acid Sequence Horses Peptide library Peptide sequence Antigens Viral Herpesviridae Infections Sequence Analysis DNA Molecular biology Epitope mapping Horse Diseases Peptides Epitope Mapping Herpesvirus 1 Equid |
| Zdroj: | Journal of virological methods. 88(1) |
| ISSN: | 0166-0934 |
| Popis: | Three filamentous phage random peptide display libraries were used in biopanning experiments with purified IgG from the serum of a gnotobiotic foal infected with equine herpesvirus-1 (EHV-1) to enrich for epitopes binding to anti-EHV-1 antibodies. The sequences of the amino acids displayed were aligned with protein sequences of EHV-1, thereby identifying a number of potential antibody binding regions. Presumptive epitopes were identified within the proteins encoded by genes 7 (DNA helicase/primase complex protein), 11 (tegument protein), 16 (glycoprotein C), 41 (integral membrane protein), 70 (glycoprotein G), 71 (envelope glycoprotein gp300), and 74 (glycoprotein E). Two groups of sequences, which aligned with either glycoprotein C (gC) or glycoprotein E (gE), identified type-specific epitopes which could be used to distinguish between sera from horses infected with either EHV-1 or EHV-4 in an ELISA using either the phage displaying the peptide or synthetic peptides as antigen. The gC epitope had been previously identified as an immunogenic region by conventional monoclonal antibody screening whereas the gE antibody binding region had not been previously identified. This demonstrates that screening of phage display peptide libraries with post-infection polyclonal sera is a suitable method for identifying diagnostic antigens for viral infections such as EHV-1. |
| Databáze: | OpenAIRE |
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