Evidence map›Paper›PMID 18402449›Full record

ArticleJournal of the American Chemical Society2008

Noncovalent cell surface engineering: incorporation of bioactive synthetic glycopolymers into cellular membranes.

David Rabuka, Martin B Forstner, Jay T Groves, Carolyn R Bertozzi

Open access · greenAbstract read
In one paragraph

Article in Journal of the American Chemical Society, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed
5.7field-weighted citation impact, top 3% 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

80 citing papers in PubMed, 199 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Synthetic Lipid Biology.Chemical reviews · 2025
    Review
  5. The Glycocalyx: The Importance of Sugar Coating the Blood-Brain Barrier.International journal of molecular sciences · 2024
    Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Mucus-Inspired Dynamic Hydrogels: Synthesis and Future Perspectives.Journal of the American Chemical Society · 2022
    Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. Human ocular mucins: The endowed guardians of sight.Advanced drug delivery reviews · 2022
    Review
  16. Glycocalyx crowding with mucin mimetics strengthens binding of soluble and virus-associated lectins to host cell glycan receptors.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  17. Chemical science · 2021
    Article
  18. Review
  19. Article
  20. Article

20 more citing papers are in PubMed but not listed here.

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 at 2 institutions in 1 country.

David RabukaDepartment of Chemistry, University of California, Berkeley, California 94720, USA.
Martin B Forstner
Jay T Groves
Carolyn R Bertozzi
Howard Hughes Medical Institute · USLawrence Berkeley National Laboratory · US

Funding

Investigations of Golgi EnzymesR01GM059907 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI BERTOZZI, CAROLYN · 1999 to 2016
$5.9M
Howard Hughes Medical InstituteNIGMS NIH HHS GM59907NIGMS NIH HHS R01 GM059907
6 · The paper itself

Abstract

The controlled addition of structurally defined components to live cell membranes can facilitate the molecular level analysis of cell surface phenomena. Here we demonstrate that cell surfaces can be engineered to display synthetic bioactive polymers at defined densities by exogenous membrane insertion. The polymers were designed to mimic native cell-surface mucin glycoproteins, which are defined by their dense glycosylation patterns and rod-like structures. End-functionalization with a hydrophobic anchor permitted incorporation into the membranes of live cultured cells. We probed the dynamic behavior of cell-bound glycopolymers bearing various hydrophobic anchors and glycan structures using fluorescence correlation spectroscopy (FCS). Their diffusion properties mirrored those of many natural membrane-associated biomolecules. Furthermore, the membrane-bound glycopolymers were internalized into early endosomes similarly to endogenous membrane components and were capable of specific interactions with protein receptors. This system provides a platform to study cell-surface phenomena with a degree of chemical control that cannot be achieved using conventional biological tools.

Indexed as

AnimalsBiomimetic MaterialsButanonesCarrier ProteinsCD55 AntigensCell MembraneCHO CellsCricetinaeCricetulusFolate Receptors, GPI-AnchoredGlycosylphosphatidylinositolsHydrophobic and Hydrophilic InteractionsMicroscopy, FluorescenceMucinsPolymersPolysaccharides3-buten-2-oneButanonesCarrier ProteinsCD55 AntigensFolate Receptors, GPI-AnchoredGlycosylphosphatidylinositolsMucinsPolymersPolysaccharidesReceptors, Cell Surface

Identifiers

PMID18402449
PMCPMC2724873
OpenAlexW1977878598

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.