Evidence map›Paper›PMID 19114638›Full record

ArticleThe Journal of general physiology2009

Molecular basis for cation selectivity in claudin-2-based paracellular pores: identification of an electrostatic interaction site.

Alan S L Yu, Mary H Cheng, Susanne Angelow, Dorothee Günzel, Sanae A Kanzawa, Eveline E Schneeberger, Michael Fromm, Rob D Coalson

Abstract read
In one paragraph

Article in The Journal of general physiology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 170 papers.

0numbers the graph read from it
0cells of the map it votes in
170citing 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

170 citing papers in PubMed.

  1. Article
  2. mSphere · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. Review
  12. Ion and water permeation through claudin-10b and claudin-15 paracellular channels.Computational and structural biotechnology journal · 2024
    Article
  13. Review
  14. Article
  15. Claudin-2 upregulation enhances intestinal permeability, immune activation, dysbiosis, and mortality in sepsis.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. Article

110 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

8 authors.

Alan S L YuDivision of Nephrology, Department of Medicine,University of Southern California Keck School of Medicine, Los Angeles, CA 90089, USA. alanyu@usc.edu
Mary H Cheng
Susanne Angelow
Dorothee Günzel
Sanae A Kanzawa
Eveline E Schneeberger
Michael Fromm
Rob D Coalson

Funding

USC RESEARCH CENTER FOR LIVER DISEASES: PILOT PROGRAMSP30DK048522 · NIDDK · UNIVERSITY OF SOUTHERN CALIFORNIA · PI KAPLOWITZ, NEIL · 1995 to 2020
$21.8M
PERMEABILITY OF THE LUNG TO WATER-SOLUBLE SOLUTESR01HL025822 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI SCHNEEBERGER, EVELINE ELSA · 1985 to 2011
$4.1M
Expression, function and regulation of renal claudinsR01DK062283 · NIDDK · UNIVERSITY OF SOUTHERN CALIFORNIA · PI YU, ALAN S · 2003 to 2010
$2.7M
NHLBI NIH HHS HL25822NHLBI NIH HHS R01 HL025822NIDDK NIH HHS DK062283NIDDK NIH HHS DK48522NIDDK NIH HHS P30 DK048522NIDDK NIH HHS R01 DK062283
6 · The paper itself

Abstract

Paracellular ion transport in epithelia is mediated by pores formed by members of the claudin family. The degree of selectivity and the molecular mechanism of ion permeation through claudin pores are poorly understood. By expressing a high-conductance claudin isoform, claudin-2, in high-resistance Madin-Darby canine kidney cells under the control of an inducible promoter, we were able to quantitate claudin pore permeability. Claudin-2 pores were found to be narrow, fluid filled, and cation selective. Charge selectivity was mediated by the electrostatic interaction of partially dehydrated permeating cations with a negatively charged site within the pore that is formed by the side chain carboxyl group of aspartate-65. Thus, paracellular pores use intrapore electrostatic binding sites to achieve a high conductance with a high degree of charge selectivity.

Indexed as

Amino Acid SequenceAnimalsBinding SitesCationsCell Membrane PermeabilityCells, CulturedClaudinsComputer SimulationDogsIon ChannelsKineticsMembrane ProteinsMiceModels, BiologicalMolecular Sequence DataMutationCationsClaudinsCldn2 protein, mouseIon ChannelsMembrane ProteinsProtein Isoforms

Identifiers

PMID19114638
PMCPMC2606938

What OpenQuestion holds

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LicenceCC BY-NC-SA
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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.