Abstract
The present paper summarizes some of our activities in the field of plasmonic DNA and genetic diagnosis, presenting our system and its capabilities before showing data related to the design and use of functionalized biochips of increasing complexity along with various experimental hybridization conditions, including solutions containing one type of purified synthetic short oligonucleotides or PCR-amplified DNA samples from patients. The diagnosis capability of our system was evaluated by detecting several point mutations that alter the function of the CFTR gene and cause cystic fibrosis, a frequent monogenic disorder selected as a clinical model system.
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Acknowledgments
The authors are thankful to past Ph.D. students, especially Nathalie Bassil, Emmanuel Maillart, and Pierre Lecaruyer, as well as postdoctorates, especially Ilaria Mannelli and Virginie Courtois. They also acknowledge the work of many other colleagues, especially Alain Bellemain and Alain Aide from Laboratoire Charles Fabry de l’Institut d’Optique (LCFIO) for the optimization of the experimental SPR imaging set-up and Laure Lecerf, Valérie Velayoudame, and Serge Pissard from Institut National de la Santé et de la Recherche Médicale (INSERM) and Mohamed Guerrouache from Systèmes Polymères Complexes (SPC) for the surface modification. The authors also acknowledge INSERM, Centre National de la Recherche Scientifique, Vaincre la Mucoviscidose [French association (Defeat CF)], and French Ministère de la Recherche for external support through funding of the research program. Jerome Hottin is currently funded as a Ph.D. student in the MaCSyBio (Material, Components, and System for Biophotonics) team of LCFIO by the GenOptics Company, localized in Orsay, France, the core activity of which is the valorization of SPRI biosensor systems.
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Hottin, J., Moreau, J., Roger, G. et al. Plasmonic DNA: Towards Genetic Diagnosis Chips. Plasmonics 2, 201–215 (2007). https://doi.org/10.1007/s11468-007-9039-6
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DOI: https://doi.org/10.1007/s11468-007-9039-6