2016
DOI: 10.1021/jacs.5b13585
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Imaging Nanostructures by Single-Molecule Localization Microscopy in Organic Solvents

Abstract: The introduction of super-resolution fluorescence microscopy (SRM) opened an unprecedented vista into nanoscopic length scales, unveiling a new degree of complexity in biological systems in aqueous environments. Regrettably, supramolecular chemistry and material science benefited far less from these recent developments. Here we expand the scope of SRM to photoactivated localization microscopy (PALM) imaging of synthetic nanostructures that are highly dynamic in organic solvents. Furthermore, we characterize th… Show more

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Cited by 30 publications
(38 citation statements)
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“…Belov and co‐workers introduced caged rhodamines NN, which, after irradiation with UV‐light, form rhodamine derivatives. These dyes have been shown to be suitable for super‐resolution microscopy in different organic solvents when a small amount of a nucleophilic solvent such as an alcohol is added . STAR and CAGE dyes have also allowed the imaging of polymeric micelles in organic solvents by both STED and SMLM .…”
Section: Fluorophoresmentioning
confidence: 99%
“…Belov and co‐workers introduced caged rhodamines NN, which, after irradiation with UV‐light, form rhodamine derivatives. These dyes have been shown to be suitable for super‐resolution microscopy in different organic solvents when a small amount of a nucleophilic solvent such as an alcohol is added . STAR and CAGE dyes have also allowed the imaging of polymeric micelles in organic solvents by both STED and SMLM .…”
Section: Fluorophoresmentioning
confidence: 99%
“…Eight male BALB/c nude mice were subcutaneously injected with 5×10 6 HeLa cells on both sides of the back. The cells injected in the left side were pre-stimulated with 80 μg/mL NPs for 24 h before digestion.…”
Section: Biocompatibility and Stability Tests In Vivo Animal Preparationmentioning
confidence: 99%
“…32 Briefly, a single cell suspension of HeLa cells was prepared for tail vein injection. Mice were intravenously injected in the tail vein using insulin syringes with 1×10 6 tumor cells in 100 μL of PBS. Before injection, based on the uptake and degradation of NPs absorbed, 33,34 the cells in the experimental group were pre-stimulated with 80 μg/mL NPs for 24 h to ensure sufficient absorption.…”
Section: Further Confirmation Of Signaling Pathways By Inhibitorsmentioning
confidence: 99%
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“…The visualization, with the above described methods, of apolar structures found in material science is often impossible since the employed polar switching buffers cannot significantly access apolar structures, whereas fluorescent proteins, if appropriate to be used, would denature under such conditions. As a consequence, super‐resolution microscopy has so far not been used extensively to address topics in soft matter or polymer science …”
Section: Introductionmentioning
confidence: 99%