Evidence map›Paper›PMID 38753144›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2024

Droplet Microfluidics with Capillary Electrophoresis for Glycan Biomarker Analysis.

Théo Liénard-Mayor, Camille Bricteux, Nguyet-Thuy Tran, Arnaud Bruneel, Myriam Taverna, Thanh Duc Mai

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Article in Methods in molecular biology (Clifton, N.J.), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Théo Liénard-MayorCNRS, Institut Galien Paris-Saclay, Université Paris-Saclay, Orsay, France.
Camille BricteuxCNRS, Institut Galien Paris-Saclay, Université Paris-Saclay, Orsay, France.
Nguyet-Thuy TranCNRS, Institut Galien Paris-Saclay, Université Paris-Saclay, Orsay, France.
Arnaud BruneelINSERM UMR1193, Université Paris-Saclay, Orsay, France.
Myriam TavernaCNRS, Institut Galien Paris-Saclay, Université Paris-Saclay, Orsay, France.
Thanh Duc MaiCNRS, Institut Galien Paris-Saclay, Université Paris-Saclay, Orsay, France. thanh-duc.mai@universite-paris-saclay.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Several glycoproteins are validated biomarkers of various diseases such as cancer, cardiovascular diseases, chronic alcohol abuse, or congenital disorders of glycosylation (CDG). In particular, CDG represent a group of more than 150 inherited diseases with varied symptoms affecting multiple organs. The distribution of glycans from target glycoprotein(s) can be used to extract information to help the diagnosis and possibly differentiate subtypes of CDG. Indeed, depending on the glycans and the proteins to which they are attached, glycans can play a very broad range of roles in both physical and biological properties of glycoproteins. For glycans in general, capillary electrophoresis with laser-induced fluorescence detection (CE-LIF) has become a staple. Analysis of glycans with CE-LIF requires several sample preparation steps, including release of glycans from the target glycoprotein, fluorescent labeling of glycans, and purification of labeled glycans. Here, we describe the protocol for glycan sample treatment in a microfluidic droplet system prior to CE-LIF of labeled glycans. The microfluidic droplet approach offers full automation, sample, and reagent volume reduction and elimination of contamination from external environment.

Indexed as

BiomarkersElectrophoresis, CapillaryPolysaccharidesGlycoproteinsGlycosylationHumansMicrofluidicsBiomarkersGlycoproteinsPolysaccharidesCapillary electrophoresisDroplet microfluidicsGlycansGlycoproteinsMagnetic beadsSample treatment

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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.