We previously reported that CSF114(Glc) detects diagnostic autoantibodies
in multiple sclerosis sera. We report herein a bioinformatic analysis of myelin proteins and
CSF114(Glc), which led to the identification of five sequences. These glucopeptides were
synthesized and tested in enzymatic assays, showing a common minimal epitope. Starting
from that, we designed an optimized sequence, SP077, showing a higher homology with
both CSF114(Glc) and the five sequences selected using the bioinformatic approach. SP077
was synthesized and tested on 50 multiple sclerosis patients’ sera, and was able to detect
higher antibody titers as compared to CSF114(Glc). Finally, the conformational properties
of SP077 were studied by NMR spectroscopy and structure calculations. Thus, the
immunological activity of SP077 in the recognition of specific autoantibodies in multiple
sclerosis patients’ sera may be ascribed to both the optimized design of its epitopic region
and the superior surface interacting properties of its C-terminal region
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