In an initial
prescreen, up to 109 random peptides displayed
on phage were screened for their binding to serum antibodies, immobilized
on beads. Next, the identified epitope peptides were validated with
solid material-based peptide microarray technology. Finally, the validated
epitopes were fine mapped by comprehensive substitution analysis.
The resulting “binding fingerprints” enable the identification
of those proteins that match the antibody specificity, and, eventually,
the correlation to disease causing agents. Reprinted with permission
from ref (146). Copyright
2017 Elsevier B.V.