Evidence map›Paper›PMID 18987344›Full record

ArticleMolecular biology of the cell2009

Molecular clustering of STIM1 with Orai1/CRACM1 at the plasma membrane depends dynamically on depletion of Ca2+ stores and on electrostatic interactions.

Nathaniel Calloway, Monika Vig, Jean-Pierre Kinet, David Holowka, Barbara Baird

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 85 papers.

0numbers the graph read from it
0cells of the map it votes in
85citing papers in PubMed
6.6field-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

85 citing papers in PubMed, 140 citations in OpenAlex.

  1. Delineating Zinc Influx Mechanisms during Platelet Activation.International journal of molecular sciences · 2023
    Article
  2. Article
  3. Article
  4. Review
  5. ER-resident STIM1/2 couples CaProceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  6. My path in the company of chemistry.Pure and applied chemistry. Chimie pure et appliquee · 2022
    Article
  7. Article
  8. Immune Synapse Residency of Orai1 Alters CaInternational journal of molecular sciences · 2021
    Article
  9. Article
  10. Cross-Talk Between the Adenylyl Cyclase/cAMP Pathway and CaReviews of physiology, biochemistry and pharmacology · 2021
    Review
  11. Article
  12. Article
  13. STIM calcium sensing and conformational change.The Journal of physiology · 2020
    Review
  14. STIM1 activation of Orai1.Cell calcium · 2019
    Review
  15. Review
  16. Article
  17. Intermittent CaeLife · 2017
    Article
  18. Article
  19. The STIM-Orai Pathway: Orai, the Pore-Forming Subunit of the CRAC Channel.Advances in experimental medicine and biology · 2017
    Review
  20. Review

25 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

5 authors at 2 institutions in 1 country.

Nathaniel CallowayDepartment of Chemistry and Chemical Biology, Cornell University, Ithaca, NY 14850, USA.
Monika Vig
Jean-Pierre Kinet
David Holowka
Barbara Baird
Cornell University · USBeth Israel Deaconess Medical Center · US

Funding

INTERACTIVE STRUCTURES AND DYNAMICS OF ANTIGEN RECEPTORSR01AI022449 · NIAID · CORNELL UNIVERSITY ITHACA · PI HOLOWKA, DAVID A · 1985 to 2014
$3.6M
NIAID NIH HHS AI-022449NIAID NIH HHS R01 AI022449
6 · The paper itself

Abstract

Activation of store operated Ca(2+) entry involves stromal interaction molecule 1 (STIM1), localized to the endoplasmic reticulum (ER), and calcium channel subunit (Orai1/CRACM1), localized to the plasma membrane. Confocal microscopy shows that thapsigargin-mediated depletion of ER Ca(2+) stores in RBL mast cells causes a redistribution of STIM1, labeled with monomeric red fluorescent protein (mRFP), to micrometer-scale ER-plasma membrane junctions that contain Orai1/CRACM1, labeled with monomeric Aequorea coerulescens green fluorescent protein (AcGFP). Using fluorescence resonance energy transfer (FRET), we determine that this visualized coredistribution is accompanied by nanoscale interaction of STIM1-mRFP and AcGFP-Orai1/CRACM1. We find that antigen stimulation of immunoglobulin E receptors causes much less Orai1/CRACM1 and STIM1 association, but strong interaction is observed under conditions that prevent refilling of ER stores. Stimulated association monitored by FRET is inhibited by sphingosine derivatives in parallel with inhibition of Ca(2+) influx. Similar structural and functional effects are caused by mutation of acidic residues in the cytoplasmic segment of Orai1/CRACM1, suggesting a role for electrostatic interactions via these residues in the coupling of Orai1/CRACM1 to STIM1. Our results reveal dynamic molecular interactions between STIM1 and Orai1/CRACM1 that depend quantitatively on electrostatic interactions and on the extent of store depletion.

Indexed as

AnimalsCalciumCalcium ChannelsCell LineCell MembraneEnzyme InhibitorsFluorescence Resonance Energy TransferMembrane GlycoproteinsORAI1 ProteinRatsRecombinant Fusion ProteinsSphingosineStatic ElectricityStromal Interaction Molecule 1ThapsigarginCalciumCalcium ChannelsEnzyme InhibitorsMembrane GlycoproteinsORAI1 ProteinOrai1 protein, ratRecombinant Fusion ProteinsSphingosineStim1 protein, ratStromal Interaction Molecule 1Thapsigargin

Identifiers

PMID18987344
PMCPMC2613096
OpenAlexW2137508826

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.