Evidence map›Paper›PMID 28231413›Full record

ArticleChembiochem : a European journal of chemical biology2017

Metabolic Chemical Reporters of Glycans Exhibit Cell-Type-Selective Metabolism and Glycoprotein Labeling.

Anna R Batt, Balyn W Zaro, Marisol X Navarro, Matthew R Pratt

Abstract read
In one paragraph

Article in Chembiochem : a European journal of chemical biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing 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

25 citing papers in PubMed.

  1. Review
  2. Iterative Bump-and-Hole Engineering Creates a Bioorthogonal Reporter forJournal of the American Chemical Society · 2026
    Article
  3. Article
  4. Review
  5. Review
  6. Iterative Bump-and-hole engineering creates a bioorthogonal reporter forbioRxiv : the preprint server for biology · 2026
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. A Bioorthogonal Precision Tool for HumanJournal of the American Chemical Society · 2024
    Article
  12. Article
  13. Article
  14. Article
  15. Recombinant mucin biotechnology and engineering.Advanced drug delivery reviews · 2023
    Review
  16. Article
  17. Article
  18. Article
  19. Chemical reporters to study mammalian O-glycosylation.Biochemical Society transactions · 2021
    Review
  20. 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

4 authors.

Anna R BattDepartment of Chemistry, University of Southern California, 840 Downey Way, LJS 250, Los Angeles, CA, 90089, USA.
Balyn W ZaroDepartment of Chemistry, University of Southern California, 840 Downey Way, LJS 250, Los Angeles, CA, 90089, USA.
Marisol X NavarroDepartment of Chemistry, University of Southern California, 840 Downey Way, LJS 250, Los Angeles, CA, 90089, USA.
Matthew R PrattDepartment of Chemistry, University of Southern California, 840 Downey Way, LJS 250, Los Angeles, CA, 90089, USA.ORCID 0000-0003-3205-5615

Funding

USC/NORRIS COMPREHENSIVE CANCER CENTER (CORE) SUPPORTP30CA014089 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Fumito Ito · 1985 to 2026
$181.4M
NCI NIH HHS P30 CA014089
6 · The paper itself

Abstract

Since the pioneering work by Reutter and co-workers that demonstrated structural flexibility in the carbohydrate biosynthesis and glycosylation pathways, many different labs have used unnatural monosaccharide analogues to perform glycan engineering on the surface of living cells. A subset of these unnatural monosaccharides contain bioorthogonal groups that enable the selective installation of visualization or enrichment tags. These metabolic chemical reporters (MCRs) have proven to be powerful for the unbiased identification of glycoproteins; however, they do have certain limitations. For example, they are incorporated substoichiometrically into glycans, and most MCRs are not selective for one class (e.g., O-GlcNAcylation) of glycoprotein. Here, we explore the relationship between the biosynthesis of MCR donor sugars in cells and the labeling levels of four different N-acetylglucosamine- and N-acetylgalactosamine-based MCRs. We found that the buildup of the different donor sugars correlated well with the overall labeling levels but less so with intracellular labeling of proteins by O-GlcNAcylation.

Indexed as

AcetylglucosamineAnimalsBiomimetic MaterialsCarbohydrate ConformationGlycoproteinsGlycosylationHEK293 CellsHeLa CellsHumansMetabolic EngineeringMiceMolecular ProbesMonosaccharidesNIH 3T3 CellsOrgan SpecificityPolysaccharidesAcetylglucosamineGlycoproteinsMolecular ProbesMonosaccharidesPolysaccharidesbioorthogonal chemistrychemical reportersglycosylationmonosaccharides

Identifiers

PMID28231413
PMCPMC5580397

What OpenQuestion holds

Textmetadata
LicenceTDM
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.