The epitope for E44 monoclonal antibody (mAb) was mapped using mutated
ETS1 proteins lacking different carboxy-terminal regions and by the e
mployment of synthetic oligopeptides spanning the epitope region. This
epitope lies around Arg211 of the human ETS1 protein since substituti
on of Arg211 by Gln211 in the epitope region results in the loss of re
cognition of the mouse ETS1 protein by E44 mAb. Substitution of Leu214
by valine214 in the epitope region (as is found in the chicken ETS1 a
nd viral Ets proteins) does not alter the capacity of the E44 mAb to r
ecognize this antigen. Taken together, these results suggest that a sp
ecific ionic interaction is able to play a pivotal role in the recogni
tion of the ETS1 protein by the E44 mAb.