2018
DOI: 10.1038/s41467-018-06740-x
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Enhanced mRNA FISH with compact quantum dots

Abstract: Fluorescence in situ hybridization (FISH) is the primary technology used to image and count mRNA in single cells, but applications of the technique are limited by photophysical shortcomings of organic dyes. Inorganic quantum dots (QDs) can overcome these problems but years of development have not yielded viable QD-FISH probes. Here we report that macromolecular size thresholds limit mRNA labeling in cells, and that a new generation of compact QDs produces accurate mRNA counts. Compared with dyes, compact QD pr… Show more

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Cited by 38 publications
(60 citation statements)
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“…Ideally, it should be reduced to the range of 5-20 nm, which will be attractive for single particle tracking and superresolution imaging, where the particle size should be comparable with biological macromolecules. [207,251] This would require dramatic shift in the design strategy, for example with the use of more compact surfactants or combination of lipids with polymers. Another aspect is related to the improving of dye encapsulation, particle brightness, and stability, which would require development of dyes with higher lipophilicity, fluorescence quantum yield and photostability as well as minimized self-quenching.…”
Section: Discussionmentioning
confidence: 99%
“…Ideally, it should be reduced to the range of 5-20 nm, which will be attractive for single particle tracking and superresolution imaging, where the particle size should be comparable with biological macromolecules. [207,251] This would require dramatic shift in the design strategy, for example with the use of more compact surfactants or combination of lipids with polymers. Another aspect is related to the improving of dye encapsulation, particle brightness, and stability, which would require development of dyes with higher lipophilicity, fluorescence quantum yield and photostability as well as minimized self-quenching.…”
Section: Discussionmentioning
confidence: 99%
“…Most disease-associated genomic mutations are base substitutions and approximately half of pathogenic human single nucleotide polymorphisms (SNPs) are related to C-to-T substitutions in the ClinVar database. 1 Base editors (BEs), which combine Cas9-D10A nickase and APOBEC (apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like) or AID (activation-induced deaminase) cytidine deaminase family members, 2 have been successfully applied to mediate C-to-T conversion in vitro and in vivo, 3 providing a powerful tool to model or repair diseaserelated human SNPs. Yet, the editing scope of BE3 was limited by the low editing efficiency at GpC dinucleotides and/or in regions with high CpG methylation levels.…”
Section: Dear Editormentioning
confidence: 99%
“…The interior of cells appeared as porous media with a throat size of ~20 nm 21 . Imaging with quantum dots of various sizes also showed dramatic signal decrease as the hydrodynamic diameter increased 22 , 23 . Importantly, these two factors are inter-related.…”
Section: Introductionmentioning
confidence: 97%