Evidence map›Paper›PMID 32146499›Full record

ArticleAnalytical and bioanalytical chemistry2020

High-throughput fluorescence correlation spectroscopy enables analysis of surface components of cell-derived vesicles.

Xu Fu, Yongwook Song, Abdullah Masud, Kanthi Nuti, Jason E DeRouchey, Christopher I Richards

Open access · greenAbstract read
In one paragraph

Article in Analytical and bioanalytical chemistry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.1field-weighted citation impact, top 24% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Exosome: an overview on enhanced biogenesis by small molecules.Naunyn-Schmiedeberg's archives of pharmacology · 2025
    Review
  5. Review
  6. Article
  7. Article
  8. Exosome Processing and Characterization Approaches for Research and Technology Development.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2022
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Xu FuDepartment of Chemistry, University of Kentucky, 161 Jacobs Science Building, Lexington, KY, 40506, USA.
Yongwook SongCenter for Computational Sciences, University of Kentucky, 325 McVey Hall, Lexington, KY, 40506, USA.
Abdullah MasudDepartment of Chemistry, University of Kentucky, 161 Jacobs Science Building, Lexington, KY, 40506, USA.
Kanthi NutiDepartment of Chemistry, University of Kentucky, 161 Jacobs Science Building, Lexington, KY, 40506, USA.
Jason E DeRoucheyDepartment of Chemistry, University of Kentucky, 161 Jacobs Science Building, Lexington, KY, 40506, USA.
Christopher I RichardsDepartment of Chemistry, University of Kentucky, 161 Jacobs Science Building, Lexington, KY, 40506, USA. chris.richards@uky.edu.ORCID http://orcid.org/0000-0003-0019-1989
University of Kentucky · US

Funding

Single molecule determination of nAChR structural assembly for therapeutic targetingR33DA038817 · NIDA · UNIVERSITY OF KENTUCKY · PI RICHARDS, CHRISTOPHER I · 2017 to 2018
$759k
National Science Foundation DBI-1556281NIDA NIH HHS R33 DA038817
6 · The paper itself

Abstract

Extracellular vesicles (EVs) and cell-derived vesicles (CDVs), generated by fragmenting cellular membranes, have both been explored as therapeutic delivery vehicles. Surface proteins on these vesicles are of great importance as they are characteristic to the cell of origin and modulate vesicle interactions with target cells. Here, we introduced a high-throughput fluorescence correlation spectroscopy (ht-FCS) approach capable of characterizing vesicle surface proteins across a large number of samples. We used automated screening and acquisition of FCS data to profile surface proteins of cell-derived vesicles with high fidelity based on changes in diffusion time upon antibody-vesicle interactions. We characterized vesicles generated from 4 cell types using antibodies for known exosome biomarkers. The ht-FCS technique presented here offers the capability to screen EVs or cell-derived vesicles against a library of surface markers or to screen a library of cell-derived vesicles for a specific identifying marker at a high speed.

Indexed as

A549 CellsAntigens, CDBiomarkersCell MembraneExosomesExtracellular VesiclesHEK293 CellsHumansMembrane ProteinsSpectrometry, FluorescenceAntigens, CDBiomarkersMembrane ProteinsCell-derived vesiclesFCSHigh-throughput screeningSurface protein composition

Identifiers

PMID32146499
PMCPMC8492160
OpenAlexW3010002587

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.