Publication | Open Access
Exploiting Fluorescence Lifetime Plasticity in FLIM: Target Molecule Localization in Cells and Tissues
39
Citations
15
References
2011
Year
NanotherapeuticsEngineeringMolecular BiologyAntagonist NaloxoneMolecular PharmacologyNanomedicineFluorescence Lifetime PlasticityTranslational Molecular ImagingBioimagingSingle MoleculeMolecular ImagingBiophysicsNovel Imaging MethodFluorescence ImagingBiological SystemsPharmacologyCell BiologySingle-molecule DetectionDrug TargetingPolymer-drug ConjugatePharmaceutical NanotechnologyDrug Delivery SystemsRmflim MethodNano-drug DeliveryCellular BiochemistryTarget Molecule LocalizationMedicineSmall MoleculesQuantitative Pharmacology
The mechanisms of drug-receptor interactions and the controlled delivery of drugs via biodegradable and biocompatible nanoparticulate carriers are active research fields in nanomedicine. Many clinically used drugs target G-protein coupled receptors (GPCRs) due to the fact that signaling via GPCRs is crucial in physiological and pathological processes and thus central for the function of biological systems. In this letter, a fast and reliable ratiometric fluorescence lifetime imaging microscopy (rmFLIM) approach is described to analyze the distribution of protein-ligand complexes in the cellular context. Binding of the fluorescently labeled antagonist naloxone to the G-protein coupled μ-opioid receptor is used as an example. To show the broad applicability of the rmFLIM method, we extended this approach to investigate the distribution of polymer-based nanocarriers in histological liver sections.
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