Diffusion Dynamics of Glycine Receptors Revealed by Single-Quantum Dot Tracking
By M. Dahan, S. Lévi, C. Luccardini, P. Rostaing, B. Riveau, A. Triller. Science, 2003
1,029 citations recorded by the source corpus.
Subfields: Cellular and Molecular Neuroscience, Electrochemistry, Materials Chemistry
View Paper: https://www.semanticscholar.org/paper/5b234b9da7ac68d46f4b4cb5ea5592dc8d62e130
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In Cellular and Molecular Neuroscience
In Materials Chemistry
- Igor L. Medintz
- H. Mattoussi
- Ron C. Hardman
- Moungi G. Bawendi
- Rakesh K. Jain
- T. Hyeon
- Edward H. Sargent
Citations in the corpus
- Comparison of the photoluminescence properties of semiconductor quantum dots and non-blinking diamond nanoparticles. Observation of the diffusion of diamond nanoparticles in living cells (2009, methodology): “In such experiments, QDs have already been used as biomarkers to study the dynamics of biomolecules [22, 23].”
- Dynamic multiple-target tracing to probe spatiotemporal cartography of cell membranes (2008, background): “has considerably increased the sensitivity of detection and greatly facilitated biological investigations of cellular processe”
- Compact high-quality CdSe/CdS core/shell nanocrystals with narrow emission linewidths and suppressed blinking (2013, methodology): “To demonstrate the benefit of using our QDs for in vivo imaging, two samples underwent the same ligand-exchange reaction (supplementary information): (1) conventional CdSe/CdS QDs (QDconv.”
- Quantum dot bioconjugates for imaging, labelling and sensing (2005, background): “These include tracking the diffusion dynamics of individual glycine receptors in neuronal cells over long periods of time (min), which provided unique information on single-protein movement, and interestingly, the authors used blinking to identify single QDs and differentiate them from aggregate”
- A Toxicologic Review of Quantum Dots: Toxicity Depends on Physicochemical and Environmental Factors (2005, background): “Dahan et al. (2003) found that QDs conjugated with glycine receptor (GlyR1) ligands exhibited specificity for endogenous GlyR1 subunits on cultured spinal neurons.”