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Luminescent Amphiphilic Aminoglycoside Probes to Study Transfection
Authors:Alexander Zimmermann  Qais Z. Jaber  Dr. Johannes Koch  Steffen Riebe  Dr. Cecilia Vallet  Dr. Kateryna Loza  Matthias Hayduk  Dr. Kfir B. Steinbuch  Prof. Shirley K. Knauer  Prof. Micha Fridman  Jun.-Prof. Jens Voskuhl
Affiliation:1. Faculty of chemistry (Organic Chemistry) and, Centre for Nanointegration Duisburg-Essen (CENIDE), University of Duisburg-Essen, Universitätsstrasse 7, 45117 Essen, Germany

These authors authors contributed equally to this work.;2. School of Chemistry, Raymond and Beverly Sackler Faculty of Exact Sciences, Tel Aviv University, Tel Aviv, 6997801 Israel;3. Center for Medical Biotechnology (ZMB), University of Duisburg Essen, Universitätsstrasse 2, 45141 Essen, Germany;4. Faculty of chemistry (Organic Chemistry) and, Centre for Nanointegration Duisburg-Essen (CENIDE), University of Duisburg-Essen, Universitätsstrasse 7, 45117 Essen, Germany;5. Institute for Molecular Biology, Centre for Medical Biotechnology (ZMB), University of Duisburg-Essen, Universitätsstrasse 2, 45117 Essen, Germany;6. Inorganic Chemistry and Centre for Nanointegration Duisburg-Essen (CeNIDE), University of Duisburg-Essen, Universitätsstrasse 7, 45141 Essen, Germany

Abstract:We report the characterization of amphiphilic aminoglycoside conjugates containing luminophores with aggregation-induced emission properties as transfection reagents. These inherently luminescent transfection vectors are capable of binding plasmid DNA through electrostatic interactions; this binding results in an emission “on” signal due to restriction of intramolecular motion of the luminophore core. The luminescent cationic amphiphiles effectively transferred plasmid DNA into mammalian cells (HeLa, HEK 293T), as proven by expression of a red fluorescent protein marker. The morphologies of the aggregates were investigated by microscopy as well as ζ-potential and dynamic light-scattering measurements. The transfection efficiencies using luminescent cationic amphiphiles were similar to that of the gold-standard transfection reagent Lipofectamine® 2000.
Keywords:aggregation-induced emission  bioimaging  cationic amphiphiles  self-assembly  transfection agents
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