Abstract
Monoclonal antibodies 6C6 and 10D5 raised against the N-terminal of β- amyloid peptide interfere with the formation of β-amyloid and trigger reversal to its non-toxic components. The epitopes of these antibodies were localized employing a library composed of filamentous phage displaying random combinatorial hexapeptides. Among 44 positive phage-clones, selected from the library by both antibodies, 40 clones carried the consensus sequence EFRH. These EFRH phage-clones bind specifically mAbs 6C6 or 10D5 with an apparent binding constant of ~ 10-9 M. The peptide EFRH inhibits binding of mAbs 6C6 or 10D5 to β-amyloid peptide in affinities identical to those obtained, with the peptides corresponding to positions 1-9, 1-16 and 1-40 of β- peptide. These findings confirm that the peptide EFRH which is located at positions 3-6 within β-amyloid peptide represents the sequential epitope of mAbs 6C6 and 10D5.
Original language | English |
---|---|
Pages (from-to) | 85-90 |
Number of pages | 6 |
Journal | Journal of Neuroimmunology |
Volume | 88 |
Issue number | 1-2 |
DOIs | |
State | Published - 1 Aug 1998 |
Keywords
- Disaggregation
- Monoclonal antibody
- N-terminal
- Sequential epitope
- β- amyloid peptide