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Sökning: WFRF:(Alizadehheidari Mohammadreza 1987) > A nano flow cytomet...

A nano flow cytometer for single lipid vesicle analysis

Friedrich, R. (författare)
Chalmers tekniska högskola,Chalmers University of Technology
Block, Stephan, 1978 (författare)
Chalmers tekniska högskola,Chalmers University of Technology
Alizadehheidari, Mohammadreza, 1987 (författare)
Chalmers tekniska högskola,Chalmers University of Technology
visa fler...
Heider, Susanne, 1984 (författare)
Chalmers tekniska högskola,Chalmers University of Technology
Fritzsche, Joachim, 1977 (författare)
Chalmers tekniska högskola,Chalmers University of Technology
Esbjörner Winters, Elin, 1978 (författare)
Chalmers tekniska högskola,Chalmers University of Technology
Westerlund, Fredrik, 1978 (författare)
Chalmers tekniska högskola,Chalmers University of Technology
Bally, Marta, 1981 (författare)
Chalmers tekniska högskola,Chalmers University of Technology
visa färre...
 (creator_code:org_t)
2017
2017
Engelska.
Ingår i: Lab on a Chip - Miniaturisation for Chemistry and Biology. - : Royal Society of Chemistry (RSC). - 1473-0189 .- 1473-0197. ; 17:5, s. 830-841
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • We present a nanofluidic device for fluorescence-based detection and characterization of small lipid vesicles on a single particle basis. The device works like a nano flow cytometer where individual vesicles are visualized by fluorescence microscopy while passing through parallel nanochannels in a pressure-driven flow. An experiment requires less than 20 mu l sample volume to quantify both the vesicle content and the fluorescence signals emitted by individual vesicles. We show that the device can be used to accurately count the number of fluorescent synthetic lipid vesicles down to a vesicle concentration of 170 fM. We also show that the size-distribution of the vesicles can be resolved from their fluorescence intensity distribution after calibration. We demonstrate the applicability of the assay in two different examples. In the first, we use the nanofluidic device to determine the particle concentration in a sample containing cell-derived extracellular vesicles labelled with a lipophilic dye. In the second, we demonstrate that dual-color detection can be used to probe peptide binding to synthetic lipid vesicles; we identify a positive membrane-curvature sensing behavior of an arginine enriched version of the Antennapedia homeodomain peptide penetratin. Altogether, these results illustrate the potential of this nanofluidic-based methodology for characterization and quantification of small biological vesicles and their interactors without ensemble averaging. The device is therefore likely to find use as a quantitative analytical tool in a variety of fields ranging from diagnostics to fundamental biology research. Moreover, our results have potential to facilitate further development of automated lab-on-a-chip devices for vesicle analysis.

Ämnesord

NATURVETENSKAP  -- Biologi -- Biofysik (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biophysics (hsv//eng)

Nyckelord

UMR168
ates of america
France.
v109
individual nanoscale liposomes
cell-penetrating peptides
fluorescence
RS
membrane curvature
Physicochim Curie
nanoparticle tracking analysis
immune-responses
Biochemistry & Molecular Biology
p8477
live cells
Paris
emerging role
Science & Technology -
amphipathic helices
extracellular vesicles
Other Topics
Chemistry

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