Abstract
Epstein-Barr virus (EBV) has been implicated in the development of many human neoplasias including B lymphomas and nasopharyngeal carcinoma (NPC). The EBV latent membrane protein 1 (LMP-1) has been found to participate in diverse cellular signaling pathways and is essential for virus-induced B-cell immortalization. In order to determine quantitatively the amount of LMP-1 in cells, five monoclonal antibodies (Mabs) specific to LMP-1 were generated. The epitopes recognized by these Mabs were found to cluster within the repeat region between the CTAR1 and CTAR2 domains, corresponding to amino acid positions 254-319 of LMP-1. These Mabs were capable of recognizing LMP-1 proteins of both lymphoid and epithelial origin as revealed by immunoblot, enzyme-linked immunosorbent assay (ELISA) and immunocytofluorescence analysis. A sandwich ELISA for the quantification of LMP-1 has been established using these Mabs. Taken together, our results indicate that the Mabs generated in this study are suitable for the detection of LMP-1 in biomedical research.
Original language | English |
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Pages (from-to) | 21-30 |
Number of pages | 10 |
Journal | Journal of Immunological Methods |
Volume | 287 |
Issue number | 1-2 |
DOIs | |
State | Published - 04 2004 |
Keywords
- 5-bromo-4-chloro-3- indolyl phosphate
- BCIP
- DMEM
- Dulbecco's modified Eagle's medium
- EBV
- ELISA
- Enzyme-linked immunosorbent assay
- Epstein-Barr virus
- FBS
- FITC
- Fetal bovine serum
- Fluorescein isothiocyanate
- LMP-1
- Monoclonal antibody
- Quantitative ELISA