Evidence map›Paper›PMID 35760821›Full record

ArticleScientific reports2022

In silico analysis of the human milk oligosaccharide glycome reveals key enzymes of their biosynthesis.

Andrew G McDonald, Julien Mariethoz, Gavin P Davey, Frédérique Lisacek

Abstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
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  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. In silico simulation of glycosylation and related pathways.Analytical and bioanalytical chemistry · 2024
    Review
  13. Article
  14. 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.

Andrew G McDonaldSchool of Biochemistry and Immunology, Trinity College Dublin, Dublin 2, Ireland. amcdonld@tcd.ie.ORCID 0000-0003-2727-176X
Julien MariethozComputer Science Department, University of Geneva, 1227, Geneva, Switzerland.ORCID 0000-0001-8974-4417
Gavin P DaveySchool of Biochemistry and Immunology, Trinity College Dublin, Dublin 2, Ireland.ORCID 0000-0002-8667-8781
Frédérique LisacekComputer Science Department, University of Geneva, 1227, Geneva, Switzerland. frederique.lisacek@unige.ch.ORCID 0000-0002-0948-4537

Funding

Swiss National Science Foundation 31003A_179249
6 · The paper itself

Abstract

Human milk oligosaccharides (HMOs) form the third most abundant component of human milk and are known to convey several benefits to the neonate, including protection from viral and bacterial pathogens, training of the immune system, and influencing the gut microbiome. As HMO production during lactation is driven by enzymes that are common to other glycosylation processes, we adapted a model of mucin-type GalNAc-linked glycosylation enzymes to act on free lactose. We identified a subset of 11 enzyme activities that can account for 206 of 226 distinct HMOs isolated from human milk and constructed a biosynthetic reaction network that identifies 5 new core HMO structures. A comparison of monosaccharide compositions demonstrated that the model was able to discriminate between two possible groups of intermediates between major subnetworks, and to assign possible structures to several previously uncharacterised HMOs. The effect of enzyme knockouts is presented, identifying β-1,4-galactosyltransferase and β-1,3-N-acetylglucosaminyltransferase as key enzyme activities involved in the generation of the observed HMO glycosylation patterns. The model also provides a synthesis chassis for the most common HMOs found in lactating mothers.

Indexed as

Gastrointestinal MicrobiomeMilk, HumanBacteriaFemaleHumansInfant, NewbornLactationOligosaccharidesOligosaccharides

Identifiers

PMID35760821
PMCPMC9237113

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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.