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Role of MHC II affinity and molecular mimicry in defining anti-HER-2/neu MAb-3 linear peptide epitope

  • Alberta Lucchese
  • , Stefan Stevanovic
  • , Animesh A. Sinha
  • , Abraham Mittelman
  • , Darja Kanduc
  • CARSO Cancer Research Center
  • University of Tübingen
  • New York Medical College

Research output: Contribution to journalArticlepeer-review

17 Scopus citations

Abstract

With the aid of computational biology, we have studied the possibility of predicting the peptides able to evoke humoral immune response by using as experimental model the human HER-2/neu breast cancer-associated antigen. We already demonstrated that HER-2/neu peptides, that are the target of humoral human and mouse immune responses, correspond to those sequences having a low degree of sequence similarity to host's proteome. Here we report that the linear peptide determinant of the anti-HER-2/neu MAb-3 is characterized by a low degree of sequence similarity to mouse proteome in combination with high binding potential to specific MHC II molecule.

Original languageEnglish
Pages (from-to)193-197
Number of pages5
JournalPeptides
Volume24
Issue number2
DOIs
StatePublished - Feb 1 2003

Keywords

  • Computational biology
  • Epitope prediction
  • HER-2/neu
  • MHC binding potential
  • Molecular mimicry

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