Photoluminescent diamond nanoparticles for cell labeling: study of the uptake mechanism in mammalian cells
arXiv:0907.1148 · doi:10.1021/nn901014j
Abstract
Diamond nanoparticles (nanodiamonds) have been recently proposed as new labels for cellular imaging. For small nanodiamonds (size <40 nm) resonant laser scattering and Raman scattering cross-sections are too small to allow single nanoparticle observation. Nanodiamonds can however be rendered photoluminescent with a perfect photostability at room temperature. Such a remarkable property allows easier single-particle tracking over long time-scales. In this work we use photoluminescent nanodiamonds of size <50 nm for intracellular labeling and investigate the mechanism of their uptake by living cells . By blocking selectively different uptake processes we show that nanodiamonds enter cells mainly by endocytosis and converging data indicate that it is clathrin mediated. We also examine nanodiamonds intracellular localization in endocytic vesicles using immunofluorescence and transmission electron microscopy. We find a high degree of colocalization between vesicles and the biggest nanoparticles or aggregates, while the smallest particles appear free in the cytosol. Our results pave the way for the use of photoluminescent nanodiamonds in targeted intracellular labeling or biomolecule delivery
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- Photophysics of single nitrogen-vacancy centers in diamond nanocrystals
- Spin-lattice relaxation of individual solid-state spins
- Tracking individual nanodiamonds in Drosophila melanogaster embryos
- Near-infrared-enhanced charge state conversion for low power optical nanoscopy with nitrogen vacancy center in diamond
- Nanoscale magnetometry through quantum control of nitrogen-vacancy centres in rotationally diffusing nanodiamonds
- Nanodiamond Landmarks for Subcellular Multimodal Optical and Electron Imaging
- Evidence of absorption dominating over scattering in light attenuation by nanodiamonds
- Lifetimes of Confined Optical Phonons and the Shape of a Raman Peak in Disordered Nanoparticles: I. Analytical Treatment
- Effects of bond disorder and surface amorphization on optical phonon lifetimes and Raman peak shape in crystalline nanoparticles
- Lifetimes of Confined Optical Phonons and the Shape of a Raman Peak in Disordered Nanoparticles: II. Numerical Treatment