2016
DOI: 10.1039/c6cc07574f
|View full text |Cite
|
Sign up to set email alerts
|

A light-up imaging protocol for neutral pH-enhanced fluorescence detection of lysosomal neuraminidase activity in living cells

Abstract: A lysosome-accessing nanoprobe is designed for recognition of lysosomal neuraminidases (Lyso-Neus), which can cleave the 4-methylumbelliferone moieties of the substrate from the nanoprobe, and lead to the escape of the moieties from acidic lysosomes into the neutral cytosol assisted by cationic poly(ethyleneimine) to light up the pH-responsive fluorescence for visual detection and dynamic tracking of Lyso-Neu activity in living cells.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

0
5
0

Year Published

2018
2018
2023
2023

Publication Types

Select...
8

Relationship

1
7

Authors

Journals

citations
Cited by 11 publications
(5 citation statements)
references
References 24 publications
0
5
0
Order By: Relevance
“…There are four mammalian sialidases, NEU1-4. Lysosomal sialidase NEU1 initiates the degradation of sialoglycoconjugates [16][17][18]; cytosolic sialidase NEU2 exhibits highest activity with gangliosides [19,20]; the plasma membrane-associated sialidase NEU3 is specific for gangliosides [21]; and sialidase NEU4, which is bound to the outer mitochondrial membranes via protein-protein interactions or occurs in the lysosomal lumen, has a wide substrate specificity from glycoproteins to gangliosides and oligosaccharides [22]. The released sialic acids are pumped back into the cytosol, where they can enter another cycle of sialyl glycoconjugate production or be broken down by N-acetylneuraminate lyase (NAL) to ManNAc and pyruvate [23].…”
mentioning
confidence: 99%
“…There are four mammalian sialidases, NEU1-4. Lysosomal sialidase NEU1 initiates the degradation of sialoglycoconjugates [16][17][18]; cytosolic sialidase NEU2 exhibits highest activity with gangliosides [19,20]; the plasma membrane-associated sialidase NEU3 is specific for gangliosides [21]; and sialidase NEU4, which is bound to the outer mitochondrial membranes via protein-protein interactions or occurs in the lysosomal lumen, has a wide substrate specificity from glycoproteins to gangliosides and oligosaccharides [22]. The released sialic acids are pumped back into the cytosol, where they can enter another cycle of sialyl glycoconjugate production or be broken down by N-acetylneuraminate lyase (NAL) to ManNAc and pyruvate [23].…”
mentioning
confidence: 99%
“…The released Neu5Ac enters into another cycle of sialoglycoconjugates in the cytosol. The main distributions of neuraminidases are the cytosol [ 29 ], lysosomal [ 30 ], mitochondria [ 31 ], plasma membrane [ 32 ], etc. Due to the lack of the specific transporter on the cell membrane, extracellular SA enters into the cell by endocytosis or pinocytosis [ 33 ].…”
Section: Main Structures Distributions and Metabolism Of Samentioning
confidence: 99%
“…The released Neu5Ac enters into another cycle of sialoglycoconjugates in the cytosol. The main distributions of neuraminidases are the cytosol [29], lysosomal [30], Meanwhile, the sialoglycoconjugates can be hydrolyzed by neuraminidase (NEU) to form Neu5Ac. The released Neu5Ac enters into another cycle of sialoglycoconjugates in the cytosol.…”
Section: Metabolism Of Samentioning
confidence: 99%
“…This strategy could be applied to monitor the ST activity during drug treatment and discriminate tumor and normal cells. To detect intracellular Neus, they delivered a lysosomal Neu-specific substrate 4-methylumbelliferyl- N -acetylneuraminic acid into lysosomes, which could release the cleavage product of 4-methylumbelliferone into the cytosol for neutral pH-enhanced fluorescence detection of lysosomal Neu activity in living cells . The designed strategy enabled the monitor of the upregulation of lysosomal Neu induced by sodium butyrate, and the dynamic tracking of the variation of lysosomal Neu activity in living cells during the apoptosis process and drug treatment.…”
Section: Intracellular Glycans Analysismentioning
confidence: 99%