Evidence map›Paper›PMID 19450477›Full record

ArticleBiophysical journal2009

A kinetic model of the inositol trisphosphate receptor based on single-channel data.

Elan Gin, Martin Falcke, Larry E Wagner, David I Yule, James Sneyd

Abstract read
In one paragraph

Article in Biophysical journal, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

  1. Article
  2. Structural titration reveals CaNature communications · 2023
    Article
  3. Modeling IPBiophysical journal · 2023
    Article
  4. An integrate-and-fire approach to CaBiophysical journal · 2023
    Article
  5. Article
  6. Review
  7. Multiscale modelling of saliva secretion.Mathematical biosciences · 2014
    Article
  8. Modelling mechanism of calcium oscillations in pancreatic acinar cells.Journal of bioenergetics and biomembranes · 2014
    Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. A dynamic model of saliva secretion.Journal of theoretical biology · 2010
    Article
  17. Article
  18. 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

5 authors.

Elan GinDepartment of Mathematics, The University of Auckland, Auckland, New Zealand.
Martin Falcke
Larry E Wagner
David I Yule
James Sneyd

Funding

[Ca2+]i and Secretory Dynamics in Parotid Acinar CellsR01DE014756 · NIDCR · UNIVERSITY OF ROCHESTER · PI David I Yule · 2002 to 2026
$9.9M
PANCREATIC SECRETION--G PROTEIN MEDIATED CA++ SIGNALINGR01DK054568 · NIDDK · UNIVERSITY OF ROCHESTER · PI YULE, DAVID I · 1998 to 2012
$3.1M
Signaling Pathways in Salivary Gland Fluid SecretionR01DE016999 · NIDCR · UNIVERSITY OF ROCHESTER · PI SHUTTLEWORTH, TREVOR J. · 2005 to 2009
$1.8M
[Ca2+]i and Secretory Dynamics in Parotid Acinar CellsR56DE014756 · NIDCR · UNIVERSITY OF ROCHESTER · PI YULE, DAVID I · 2007 to 2007
$395k
Pancreatic Function: G-Protein Mediated Ca2+ SignalingR56DK054568 · NIDDK · UNIVERSITY OF ROCHESTER · PI YULE, DAVID I · 2007 to 2007
$347k
NIDCR NIH HHS DE14756NIDCR NIH HHS R01 DE014756NIDCR NIH HHS R01 DE016999NIDCR NIH HHS R01 DE016999-01NIDCR NIH HHS R56 DE014756NIDDK NIH HHS DK54568NIDDK NIH HHS R01 DK054568NIDDK NIH HHS R56 DK054568
6 · The paper itself

Abstract

In many cell types, the inositol trisphosphate receptor is one of the important components controlling intracellular calcium dynamics, and an understanding of this receptor is necessary for an understanding of calcium oscillations and waves. Based on single-channel data from the type-I inositol trisphosphate receptor, and using a Markov chain Monte Carlo approach, we show that the most complex time-dependent model that can be unambiguously determined from steady-state data is one with three closed states and one open state, and we determine how the rate constants depend on calcium. Because the transitions between these states are complex functions of calcium concentration, each model state must correspond to a group of physical states. We fit two different topologies and find that both models predict that the main effect of [Ca(2+)] is to modulate the probability that the receptor is in a state that is able to open, rather than to modulate the transition rate to the open state.

Indexed as

Models, BiologicalAnimalsBayes TheoremCalciumCell LineInositol 1,4,5-Trisphosphate ReceptorsIon Channel GatingKineticsMarkov ChainsMonte Carlo MethodPhosphorylationRatsCalciumInositol 1,4,5-Trisphosphate Receptors

Identifiers

PMID19450477
PMCPMC2712151

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.