Abstract
An antigenic mimic of the Ebola glycoprotein was synthesized and tested for its ability to be recognized by an anti-Ebola glycoprotein antibody. Epitope-mapping procedures yielded a suitable epitope that, when presented on the surface of a nanoparticle, forms a structure that is recognized by an antibody specific for the native protein. This mimic-antibody interaction has been quantitated through ELISA and QCM-based methods and yielded an affinity (Kd = 12 × 10−6 M) within two orders of magnitude of the reported affinity of the native Ebola glycoprotein for the same antibody. These results suggest that the rational design approach described herein is a suitable method for the further development of protein-based antigenic mimics with potential applications in vaccine development and sensor technology.
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Acknowledgments
This work is funded in part by the National Institutes of Health (NIH; Grant RO1 GM 076479) and the NIH Southeast Regional Center of Excellence for Biodefense (Grant 5 U54 AI57157). We also acknowledge Larry Liao and Bart Haynes for providing the monoclonal antibody 15H10.
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Appendix: Design and Synthesis of an Immunological Mimic of the Ebola Glycoprotein
Appendix: Design and Synthesis of an Immunological Mimic of the Ebola Glycoprotein
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Rutledge, R.D., Huffman, B.J., Cliffel, D.E. et al. Design and synthesis of an antigenic mimic of the Ebola glycoprotein. Journal of Materials Research 23, 3161–3168 (2008). https://doi.org/10.1557/JMR.2008.0384
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DOI: https://doi.org/10.1557/JMR.2008.0384