alpha-latrotoxin (alpha-LTX) binding sites to functionally active monoclona
l antibodies (MA) A4 and A24 were localized using three approaches: hydroly
sis of the toxin followed by the N-terminal sequencing of immunoreactive pe
ptides; the study of antibody interaction with several recombinant alpha-LT
X fragments; and Western immunoblotting of synthetic overlapping peptides (
6-8 aa) whose structures correspond to that of the immunoreactive alpha-LTX
fragment. It was shown that the MA A4 epitope is located within the F-234-
M-294 protein fragment and that of MA A24 interacts with the fragment (FDKD
IT352)-F-347.