Evidence map›Paper›PMID 31216664›Full record

ArticleMolecules (Basel, Switzerland)2019

Investigation of the Binding Affinity of a Broad Array of l-Fucosides with Six Fucose-Specific Lectins of Bacterial and Fungal Origin.

Son Thai Le, Lenka Malinovska, Michaela Vašková, Erika Mező, Viktor Kelemen, Anikó Borbás, Petr Hodek, Michaela Wimmerová, Magdolna Csávás

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.8field-weighted citation impact, top 34% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. 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

9 authors at 3 institutions in 2 countries.

Son Thai LeDepartment of Pharmaceutical Chemistry, University of Debrecen, Egyetem tér 1, H-4032 Debrecen, Hungary. le.thai.son@pharm.unideb.hu.ORCID 0000-0001-5260-7486
Lenka MalinovskaCentral European Institute of Technology, Masaryk University, Kamenice 5, 625 00 Brno, Czech Republic. malinovska@mail.muni.cz.ORCID 0000-0002-4211-3033
Michaela VaškováDepartment of Biochemistry, Faculty of Science, Charles University, Albertov 2030, 128 40 Prague 2, Czech Republic. michael.vaskova@gmail.com.
Erika MezőDepartment of Pharmaceutical Chemistry, University of Debrecen, Egyetem tér 1, H-4032 Debrecen, Hungary. mezo.erika@science.unideb.hu.
Viktor KelemenDepartment of Pharmaceutical Chemistry, University of Debrecen, Egyetem tér 1, H-4032 Debrecen, Hungary. kelemen.viktor@pharm.unideb.hu.
Anikó BorbásDepartment of Pharmaceutical Chemistry, University of Debrecen, Egyetem tér 1, H-4032 Debrecen, Hungary. borbas.aniko@pharm.unideb.hu.ORCID 0000-0001-8462-4547
Petr HodekDepartment of Biochemistry, Faculty of Science, Charles University, Albertov 2030, 128 40 Prague 2, Czech Republic. petr.hodek@natur.cuni.cz.
Michaela WimmerováCentral European Institute of Technology, Masaryk University, Kamenice 5, 625 00 Brno, Czech Republic. michaw@chemi.muni.cz.
Magdolna CsávásDepartment of Pharmaceutical Chemistry, University of Debrecen, Egyetem tér 1, H-4032 Debrecen, Hungary. michaela.wimmerova@ceitec.muni.cz.
University of Debrecen · HUCentral European Institute of Technology · CZCharles University · CZ

Funding

Czech Science Foundation 15-17572SEU and the European Regional Development Fund GINOP-2.3.2-15-2016-00008Hungarian Academy of Sciences János Bolyai FellowshipMinistry of Education, Youth and Sports CIISB research infrastructure LM2015043Ministry of Human Capacities New National Excellence Program, ÚNKP-18-4, Bolyai +National Research and Development and Innovation Office of Hungary K119509National Research and Development and Innovation Office of Hungary TÉT_15_IN-1-2016-0071
6 · The paper itself

Abstract

Series of multivalent α-l-fucoside containing glycoclusters and variously decorated l-fucosides were synthesized to find potential inhibitors of fucose-specific lectins and study the structure-binding affinity relationships. Tri- and tetravalent fucoclusters were built using copper-mediated azide-alkyne click chemistry. Series of fucoside monomers and dimers were synthesized using various methods, namely glycosylation, an azide-alkyne click reaction, photoinduced thiol-en addition, and sulfation. The interactions between compounds with six fucolectins of bacterial or fungal origin were tested using a hemagglutination inhibition assay. As a result, a tetravalent, α-l-fucose presenting glycocluster showed to be a ligand that was orders of magnitude better than a simple monosaccharide for tested lectins in most cases, which can nominate it as a universal ligand for studied lectins. This compound was also able to inhibit the adhesion of

Indexed as

Bacterial ProteinsFucoseFungal ProteinsHemagglutinationHemagglutination Inhibition TestsHumansLectinsProtein BindingStructure-Activity RelationshipBacterial ProteinsFucosefucose-binding lectinFungal ProteinsLectinscystic fibrosisglycoclustershemagglutinationlectinsl-fucosidesmultivalency

Identifiers

PMID31216664
PMCPMC6631993
OpenAlexW2949195782

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.