Evidence map›Paper›PMID 25030450›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2014

Enhanced receptor-clathrin interactions induced by N-glycan-mediated membrane micropatterning.

Juan A Torreno-Pina, Bruno M Castro, Carlo Manzo, Sonja I Buschow, Alessandra Cambi, Maria F Garcia-Parajo

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
5.0field-weighted citation impact, top 4% 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

34 citing papers in PubMed, 75 citations in OpenAlex.

  1. Article
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  11. Seminal Plasma Glycoproteins as Potential Ligands of Lectins Engaged in Immunity Regulation.International journal of environmental research and public health · 2022
    Review
  12. Stochastic particle unbinding modulates growth dynamics and size of transcription factor condensates in living cells.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Flow Arrest in the Plasma Membrane.Biophysical journal · 2019
    Article
  19. Article
  20. 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

6 authors at 4 institutions in 2 countries.

Juan A Torreno-PinaICFO-Institut de Ciencies Fotoniques, 08860 Castelldefels, Spain;
Bruno M CastroICFO-Institut de Ciencies Fotoniques, 08860 Castelldefels, Spain;
Carlo ManzoICFO-Institut de Ciencies Fotoniques, 08860 Castelldefels, Spain;
Sonja I BuschowDepartment of Tumour Immunology, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, 6500, HB Nijmegen, The Netherlands;
Alessandra CambiDepartment of Tumour Immunology, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, 6500, HB Nijmegen, The Netherlands;Nanobiophysics, MESA+ Institute for Nanotechnology and MIRA Institute for Biomedical Technology and Technical Medicine, University of Twente, 7500 AE, Enschede, The Netherlands; and.
Maria F Garcia-ParajoICFO-Institut de Ciencies Fotoniques, 08860 Castelldefels, Spain;ICREA-Institució Catalana de Recerca i Estudis Avançats, 08010 Barcelona, Spain maria.garcia-parajo@icfo.es.
Institute of Photonic Sciences · ESInstitució Catalana de Recerca i Estudis Avançats · ESRadboud Institute for Molecular Life Sciences · NLRadboud University Nijmegen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glycan-protein interactions are emerging as important modulators of membrane protein organization and dynamics, regulating multiple cellular functions. In particular, it has been postulated that glycan-mediated interactions regulate surface residence time of glycoproteins and endocytosis. How this precisely occurs is poorly understood. Here we applied single-molecule-based approaches to directly visualize the impact of glycan-based interactions on the spatiotemporal organization and interaction with clathrin of the glycosylated pathogen recognition receptor dendritic cell-specific intercellular adhesion molecule-3-grabbing nonintegrin (DC-SIGN). We find that cell surface glycan-mediated interactions do not influence the nanoscale lateral organization of DC-SIGN but restrict the mobility of the receptor to distinct micrometer-size membrane regions. Remarkably, these regions are enriched in clathrin, thereby increasing the probability of DC-SIGN-clathrin interactions beyond random encountering. N-glycan removal or neutralization leads to larger membrane exploration and reduced interaction with clathrin, compromising clathrin-dependent internalization of virus-like particles by DC-SIGN. Therefore, our data reveal that cell surface glycan-mediated interactions add another organization layer to the cell membrane at the microscale and establish a novel mechanism of extracellular membrane organization based on the compartments of the membrane that a receptor is able to explore. Our work underscores the important and complex role of surface glycans regulating cell membrane organization and interaction with downstream partners.

Indexed as

AnimalsCell Adhesion MoleculesCHO CellsClathrinCricetinaeCricetulusDC-Specific ICAM-3 Grabbing NonintegrinHumansLectins, C-TypeMembrane MicrodomainsPolysaccharidesReceptors, Cell SurfaceCell Adhesion MoleculesClathrinDC-Specific ICAM-3 Grabbing NonintegrinLectins, C-TypePolysaccharidesReceptors, Cell Surfacecell membrane compartmentalizationclathrin-dependent endocytosispathogen receptor DC-SIGNprotein glycosylationSTED nanoscopy

Identifiers

PMID25030450
PMCPMC4121791
OpenAlexW2129051779

What OpenQuestion holds

Textmetadata
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.