Evidence map›Paper›PMID 33480417›Full record

ArticleThe Biochemical journal2021

Mobility shift-based electrophoresis coupled with fluorescent detection enables real-time enzyme analysis of carbohydrate sulfatase activity.

Dominic P Byrne, James A London, Patrick A Eyers, Edwin A Yates, Alan Cartmell

Erratum issuedAbstract readComparative StudyEvaluation Study
In one paragraph

Article in The Biochemical journal, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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.

  1. Article
  2. Article
  3. Arylsulfamates inhibit colonic Bacteroidota growth through a sulfatase-independent mechanism.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  4. Review
  5. Article
  6. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Dominic P ByrneDepartment of Biochemistry and Systems Biology, Institute of Systems, Molecular and Integrative Biology, Biosciences Building, Crown Street, University of Liverpool, Liverpool L69 7ZB, U.K.
James A LondonDepartment of Biochemistry and Systems Biology, Institute of Systems, Molecular and Integrative Biology, Biosciences Building, Crown Street, University of Liverpool, Liverpool L69 7ZB, U.K.
Patrick A EyersDepartment of Biochemistry and Systems Biology, Institute of Systems, Molecular and Integrative Biology, Biosciences Building, Crown Street, University of Liverpool, Liverpool L69 7ZB, U.K.
Edwin A YatesDepartment of Biochemistry and Systems Biology, Institute of Systems, Molecular and Integrative Biology, Biosciences Building, Crown Street, University of Liverpool, Liverpool L69 7ZB, U.K.
Alan CartmellDepartment of Biochemistry and Systems Biology, Institute of Systems, Molecular and Integrative Biology, Biosciences Building, Crown Street, University of Liverpool, Liverpool L69 7ZB, U.K.

Funding

Biotechnology and Biological Sciences Research Council BB/M011186/1Biotechnology and Biological Sciences Research Council BB/N021703/1Biotechnology and Biological Sciences Research Council BB/S018514/1Wellcome Trust
6 · The paper itself

Abstract

Sulfated carbohydrate metabolism is a fundamental process, which occurs in all domains of life. Carbohydrate sulfatases are enzymes that remove sulfate groups from carbohydrates and are essential to the depolymerisation of complex polysaccharides. Despite their biological importance, carbohydrate sulfatases are poorly studied and challenges remain in accurately assessing the enzymatic activity, specificity and kinetic parameters. Most notably, the separation of desulfated products from sulfated substrates is currently a time-consuming process. In this paper, we describe the development of rapid capillary electrophoresis coupled to substrate fluorescence detection as a high-throughput and facile means of analysing carbohydrate sulfatase activity. The approach has utility for the determination of both kinetic and inhibition parameters and is based on existing microfluidic technology coupled to a new synthetic fluorescent 6S-GlcNAc carbohydrate substrate. Furthermore, we compare this technique, in terms of both time and resources, to high-performance anion exchange chromatography and NMR-based methods, which are the two current 'gold standards' for enzymatic carbohydrate sulfation analysis. Our study clearly demonstrates the advantages of mobility shift assays for the quantification of near real-time carbohydrate desulfation by purified sulfatases, and will support the search for small molecule inhibitors of these disease-associated enzymes.

Indexed as

Bacterial ProteinsBacteroides thetaiotaomicronBoron CompoundsCarbohydrate ConformationChromatography, High Pressure LiquidChromatography, Ion ExchangeComputer SystemsElectrophoresis, CapillaryElectrophoretic Mobility Shift AssayFluorescent DyesFluorometryGlycosaminoglycansHigh-Throughput Screening AssaysKineticsMicrofluidic Analytical TechniquesNuclear Magnetic Resonance, BiomolecularBacterial ProteinsBoron CompoundsFluorescent DyesGlycosaminoglycansRecombinant ProteinsSulfotransferasescarbohydrate sulfatasesenzymologyglycosaminoglycansHPAECinhibitorNMR

Identifiers

PMID33480417
PMCPMC7897442

What Socratic holds

Textmetadata
LicenceCC BY
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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 Socratic graph.