A. Lecroisey et al., NMR-STUDIES ON THE FLEXIBILITY OF THE POLIOVIRUS C3 LINEAR EPITOPE INSERTED INTO DIFFERENT SITES OF THE MALTOSE-BINDING PROTEIN, The Journal of biological chemistry, 272(1), 1997, pp. 362-368
A set of permissive positions that tolerate insertions/deletions witho
ut major deleterious consequences for the binding activity of the prot
ein was previously identified in the maltose-binding protein, The C3 e
pitope from poliovirus VP1 protein ((93)DNPASTTNKDK(103)) was inserted
into eight of these positions and two nonpermissive control sites, NM
R studies were performed on the MalE protein, the insertion/deletion m
utants, and the C3MalE hybrids to selectively determine the flexible r
egions in these proteins. Comparison of the C3 epitope mobility in the
different hybrid proteins indicates that, whatever its insertion site
and independently from the specific sequences of its linkers, the epi
tope is mostly flexible, The vector protein was shown to unfold partia
lly only in the two C3MalE hybrids that correspond to nonpermissive po
sitions, For one of them (insertion at site 339), both sides of the in
sert are flexible, and at most one side for all the other hybrids, Thi
s result correlates with the antigenicity data on the inserted epitope
(Martineau, P., Leclerc, C., and Hofnung, M. (1997) Mol. Immunol, in
press.