2018
DOI: 10.1016/j.bbagen.2018.02.001
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Facile metabolic glycan labeling strategy for exosome tracking

Abstract: A facile and effective exosome labeling strategy was introduced by presenting azido moiety on the surface of exosome through metabolic glycan synthesis, and then conjugating a strain-promoted fluorescent dye.

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Cited by 72 publications
(55 citation statements)
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References 43 publications
(47 reference statements)
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“…Especially, genetically labeled exosomes can be utilized to monitor the effects of surface modifications, such as covalent binding or membrane integration, which may cause structural or functional changes in the membranes of exosomes [67]. [74,76] Labeling of exosomes by encapsulation has been performed with various labeling probes such as radioisotopes, nanoparticles, and fluorescent dyes ( Table 4). Passive loading of probes is frequently used.…”
Section: Labeling Methodsmentioning
confidence: 99%
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“…Especially, genetically labeled exosomes can be utilized to monitor the effects of surface modifications, such as covalent binding or membrane integration, which may cause structural or functional changes in the membranes of exosomes [67]. [74,76] Labeling of exosomes by encapsulation has been performed with various labeling probes such as radioisotopes, nanoparticles, and fluorescent dyes ( Table 4). Passive loading of probes is frequently used.…”
Section: Labeling Methodsmentioning
confidence: 99%
“…To avoid this, methods based on the gel filtration (GF) principle are possible alternatives to conventional SEC. Commercial GF columns are already available to remove free probes by simple centrifugation without a significant increase in the sample volume [44,74,82,97]. Precipitation methods were also used to remove free probes.…”
Section: Exosome Isolation Methodsmentioning
confidence: 99%
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“…Tetraacetylated N-azidoacetyl-D-mannosamine (Ac4ManNAz) is placed in culture with the parent cells, spontaneously incorporated into glycans and uniformly redistributed on their EVs. The azido-EVs are then labeled with azadibenzylcyclooctyne (ADIBO)-fluorescent dyes by a bioorthogonal click reaction [133]. Exploiting the principle of bioluminescence for tracking EVs, in vivo Gaussian Luciferase (Gluc) is linked to a transmembrane domain of a platelet-derived growth factor receptor [134,135], or a lactadherin [136,137].…”
Section: Indirect Surface Functionalizationmentioning
confidence: 99%
“…in vivo tracking of fluorescent labeled cancer-derived exosomes were evaluated in various cells (MCF7 and MDA-MB-231 cells) and tumor bearing mice. Highly metastatic cancer-derived exosomes homed to the tumor and showed selective organ distribution in vivo (mostly in the liver and intestines) (Lee et al, 2018). Taken together, although FLI has drawbacks such as low penetration depth, labeling exosomes with fluorescent indicators provides information not merely about biodistribution and migration abilities of the exosomes, but also on the biological mechanisms that occur in the cell and involve exosomes biogenesis, secretion and communication with high resolution.…”
Section: Optical Imagingmentioning
confidence: 99%