Evidence map›Paper›PMID 25299151›Full record

ArticleAnalytical chemistry2014

Liquid chromatography-selected reaction monitoring (LC-SRM) approach for the separation and quantitation of sialylated N-glycans linkage isomers.

Shujuan Tao, Yining Huang, Barry E Boyes, Ron Orlando

Abstract read
In one paragraph

Article in Analytical chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

26 citing papers in PubMed, 65 citations in OpenAlex.

  1. Glycosylation in kidney diseases.Precision clinical medicine · 2025
    Review
  2. Article
  3. Targeted Analysis of Permethylated N-Glycans Using MRM/PRM Approaches.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  4. Article
  5. Article
  6. Review
  7. An Efficient and EconomicalMetabolites · 2022
    Article
  8. Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Glycan-specific precipitation of glycopeptides in high organic content sample solvents used in HILIC.Journal of chromatography. B, Analytical technologies in the biomedical and life sciences · 2020
    Article
  14. Article
  15. Sialic acid derivatization for glycan analysis by mass spectrometry.Proceedings of the Japan Academy. Series B, Physical and biological sciences · 2019
    Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. 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

4 authors at 2 institutions in 1 country.

Shujuan TaoComplex Carbohydrate Research Center, University of Georgia , Athens, Georgia 30602, United States.
Yining Huang
Barry E Boyes
Ron Orlando
University of Georgia · USAdvanced Materials Technology (United States) · US

Funding

ZINC DEFICIENCY &PROTEIN EXPRESSION IN RAT OLFACTORY BULBSP41RR018502 · NCRR · UNIVERSITY OF GEORGIA (UGA) · PI PIERCE, J. MICHAEL · 2003 to 2011
$13.1M
Novel Materials and Methods for Separations of Glycopeptides and GlycansR44GM093747 · NIGMS · ADVANCED MATERIALS TECHNOLOGY, INC. · PI BOYES, BARRY E · 2013 to 2015
$1.2M
Site-specific O-GlcNAc MAbs: New Tools for GlycoproteomicsR41GM104631 · NIGMS · GLYCOSCIENTIFIC, LLC · PI ORLANDO, RON · 2012 to 2013
$624k
NCRR NIH HHS P41 RR018502NCRR NIH HHS P41RR018502NIGMS NIH HHS R41 GM104631NIGMS NIH HHS R41GM104631-01NIGMS NIH HHS R44 GM093747NIGMS NIH HHS R44GM093747-02
6 · The paper itself

Abstract

The study of N-linked glycans is among the most challenging bioanalytical tasks because of their complexity and variety. The presence of glycoform families that differ only in branching and/or linkage position makes the identification and quantitation of individual glycans exceedingly difficult. Quantitation of these individual glycans is important because changes in the abundance of these isomers are often associated with significant biomedical events. For instance, previous studies have shown that the ratio of α2-3 to α2-6 linked sialic acid (SA) plays an important role in cancer biology. Consequently, quantitative methods to detect alterations in the ratios of glycans based on their SA linkages could serve as a diagnostic tool in oncology, yet traditional glycomic profiling cannot readily differentiate between these linkage isomers. Here, we present a liquid chromatography-selected reaction monitoring (LC-SRM) approach that we demonstrate is capable of quantitating the individual SA linkage isomers. The LC method is capable of separating sialylated N-glycan isomers differing in α2-3 and α2-6 linkages using a novel superficially porous particle (Fused-Core) Penta-HILIC (hydrophilic interaction liquid chromatography) column. SRM detection provides the relative quantitation of each SA linkage isomer, and minimizes interferences from coeluting glycans that are problematic for UV/Fluorescence based quantitation. With our approach, the relative quantitation of each SA linkage isomer is obtained from a straightforward liquid chromatography-mass spectrometry (LC-MS) experiment.

Indexed as

AnimalsCarbohydrate SequenceCattleChromatography, LiquidFetuinsHumansIsomerismMass SpectrometryMolecular Sequence DataPolysaccharidesSerumSialic AcidsFetuinsPolysaccharidesSialic Acids

Identifiers

PMID25299151
PMCPMC4222624
OpenAlexW2325347979

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.