Evidence map›Paper›PMID 31719635›Full record

ArticleScientific reports2019

Salt-free fractionation of complex isomeric mixtures of glycosaminoglycan oligosaccharides compatible with ESI-MS and microarray analysis.

Hao Liu, Apoorva Joshi, Pradeep Chopra, Lin Liu, Geert-Jan Boons, Joshua S Sharp

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.9field-weighted citation impact, top 29% 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

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Analysis of the Glycosaminoglycan Chains of Proteoglycans.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2021
    Review
  6. Article
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 2 institutions in 2 countries.

Hao LiuDepartment of BioMolecular Sciences, University of Mississippi, Oxford, MS, 38677, USA.
Apoorva JoshiDepartment of Chemistry, University of Georgia, Athens, GA, 30602, USA.
Pradeep ChopraComplex Carbohydrate Research Center, University of Georgia, Athens, GA, 30602, USA.
Lin LiuComplex Carbohydrate Research Center, University of Georgia, Athens, GA, 30602, USA.ORCID http://orcid.org/0000-0002-0310-5946
Geert-Jan BoonsDepartment of Chemistry, University of Georgia, Athens, GA, 30602, USA.ORCID http://orcid.org/0000-0003-3111-5954
Joshua S SharpDepartment of BioMolecular Sciences, University of Mississippi, Oxford, MS, 38677, USA. jsharp@olemiss.edu.
University of Georgia · USUniversity of Mississippi · US

Funding

TR&D3. Approaches to Proteoglycan Function at Biochemical and Cellular LevelsP41GM103390 · NIGMS · UNIVERSITY OF GEORGIA · PI MOREMEN, KELLEY W. · 2012 to 2019
$14.5M
NIGMS NIH HHS P41 GM103390
6 · The paper itself

Abstract

Heparin and heparan sulfate (Hp/HS) are linear complex glycosaminoglycans which are involved in diverse biological processes. The structural complexity brings difficulties in separation, making the study of structure-function relationships challenging. Here we present a separation method for Hp/HS oligosaccharide fractionation with cross-compatible solvent and conditions, combining size exclusion chromatography (SEC), ion-pair reversed phase chromatography (IPRP), and hydrophilic interaction chromatography (HILIC) as three orthogonal separation methods that do not require desalting or extensive sample handling. With this method, the final eluent is suitable for structure-function relationship studies, including tandem mass spectrometry and microarray printing. Our data indicate that high resolution is achieved on both IPRP and HILIC for Hp/HS isomers. In addition, the fractions co-eluted in IPRP could be further separated by HILIC, with both separation dimensions capable of resolving some isomeric oligosaccharides. We demonstrate this method using both unpurified reaction products from isomeric synthetic hexasaccharides and an octasaccharide fraction from enoxaparin, identifying isomers resolved by this multi-dimensional separation method. We demonstrate both structural analysis by MS, as well as functional analysis by microarray printing and screening using a prototypical Hp/HS binding protein: basic-fibroblast growth factor (FGF2). Collectively, this method provides a strategy for efficient Hp/HS structure-function characterization.

Indexed as

Microarray AnalysisSpectrometry, Mass, Electrospray IonizationBenzamidesChemical FractionationEnoxaparinFibroblast Growth Factor 2GlycosaminoglycansHeparan SulfateHeparinHumansHydrophobic and Hydrophilic InteractionsIsomerismOligosaccharidesReproducibility of Results2-amino-N-(2-aminoethyl)benzamideBenzamidesEnoxaparinFibroblast Growth Factor 2GlycosaminoglycansHeparan SulfateHeparinOligosaccharides

Identifiers

PMID31719635
PMCPMC6851191
OpenAlexW2985302660

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Registered trials

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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.