Evidence map›Paper›PMID 29802667›Full record

ArticleAngewandte Chemie (International ed. in English)2018

Chemoenzymatic Assembly of Mammalian O-Mannose Glycans.

Caicai Meng, Aniruddha Sasmal, Yan Zhang, Tian Gao, Chang-Cheng Liu, Naazneen Khan, Ajit Varki, Fengshan Wang, Hongzhi Cao

Open access · greenAbstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.0field-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

17 citing papers in PubMed, 53 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Sialoglycan-binding patterns of bacterial ABThe Journal of biological chemistry · 2022
    Article
  8. Article
  9. Article
  10. TheJournal of proteome research · 2021
    Article
  11. Review
  12. Article
  13. Terminal Epitope-Dependent Branch Preference of Siglecs TowardFrontiers in molecular biosciences · 2021
    Article
  14. Nucleotide Sugars in Chemistry and Biology.Molecules (Basel, Switzerland) · 2020
    Review
  15. Review
  16. Review
  17. Synthesis ofFrontiers in immunology · 2019
    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

9 authors at 2 institutions in 2 countries.

Caicai MengNational Glycoengineering Research Center, School of Pharmaceutical Science, Shandong University, Jinan, 250012, China.
Aniruddha SasmalGlycobiology Research and Training Center, University of California, San Diego, CA, 92093, USA.
Yan ZhangNational Glycoengineering Research Center, School of Pharmaceutical Science, Shandong University, Jinan, 250012, China.
Tian GaoNational Glycoengineering Research Center, School of Pharmaceutical Science, Shandong University, Jinan, 250012, China.
Chang-Cheng LiuNational Glycoengineering Research Center, School of Pharmaceutical Science, Shandong University, Jinan, 250012, China.
Naazneen KhanGlycobiology Research and Training Center, University of California, San Diego, CA, 92093, USA.
Ajit VarkiGlycobiology Research and Training Center, University of California, San Diego, CA, 92093, USA.
Fengshan WangNational Glycoengineering Research Center, School of Pharmaceutical Science, Shandong University, Jinan, 250012, China.
Hongzhi CaoNational Glycoengineering Research Center, School of Pharmaceutical Science, Shandong University, Jinan, 250012, China.ORCID 0000-0003-4736-3143
Shandong University · CNUniversity of California San Diego · US

Funding

BIOSYNTHESIS AND REGULATION OF SUBSTITUTED SIALIC ACIDSR01GM032373 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI VARKI, AJIT P · 1985 to 2022
$6.9M
NIGMS NIH HHS R01 GM032373
6 · The paper itself

Abstract

O-Mannose glycans account up to 30 % of total O-glycans in the brain. Previous synthesis and functional studies have only focused on the core M3 O-mannose glycans of α-dystroglycan, which are a causative factor for various muscular diseases. In this study, a highly efficient chemoenzymatic strategy was developed that enabled the first collective synthesis of 63 core M1 and core M2 O-mannose glycans. This chemoenzymatic strategy features the gram-scale chemical synthesis of five judiciously designed core structures, and the diversity-oriented modification of the core structures with three enzyme modules to provide 58 complex O-mannose glycans in a linear sequence that does not exceed four steps. The binding profiles of synthetic O-mannose glycans with a panel of lectins, antibodies, and brain proteins were also explored by using a printed O-mannose glycan array.

Indexed as

AnimalsBiocatalysisChemistry Techniques, SyntheticDystroglycansGlycosylationGlycosyltransferasesHumansMannosePolysaccharidesDystroglycansGlycosyltransferasesMannosePolysaccharideschemoenzymatic synthesisdystroglycanglycosylationglycosyltransferasesO-mannose glycans

Identifiers

PMID29802667
PMCPMC6176721
OpenAlexW2804233392

What OpenQuestion holds

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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 OpenQuestion graph.