Evidence map›Paper›PMID 24314079›Full record

ArticleBiophysical journal2013

Short-chain phosphoinositide partitioning into plasma membrane models.

Marcus D Collins, Sharona E Gordon

Open access · bronzeAbstract read
In one paragraph

Article in Biophysical journal, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

21 citing papers in PubMed, 27 citations in OpenAlex.

  1. PtdIns(3,5)PNature · 2026
    Article
  2. PtdIns(3,5)PbioRxiv : the preprint server for biology · 2025
    Article
  3. Article
  4. Phosphatidylinositol 3,5-bisphosphate regulates CaTraffic (Copenhagen, Denmark) · 2020
    Article
  5. Article
  6. The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
  7. Article
  8. Article
  9. Article
  10. Regulation of thermoTRPs by lipids.Temperature (Austin, Tex.) · 2017
    Review
  11. Article
  12. Article
  13. Article
  14. Phosphoinositide regulation of TRPV1 revisited.Pflugers Archiv : European journal of physiology · 2015
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Marcus D CollinsUniversity of Washington School of Medicine, Department of Physiology and Biophysics, Seattle, WA.
Sharona E Gordon
University of Washington · US

Funding

Inflammatory hyperalgesia mediated by TRPV1, the pepper spray receptor in the corR01EY017564 · NEI · UNIVERSITY OF WASHINGTON · PI GORDON, SHARONA E · 2006 to 2022
$6.5M
FUNCTIONAL ARCHITECTURE OF RETINAL ROD CNG ION CHANNELSR01EY013007 · NEI · UNIVERSITY OF WASHINGTON · PI GORDON, SHARONA E · 1999 to 2006
$2.7M
Mechanisms of TRPV1 Channel RegulationR01GM100718 · NIGMS · UNIVERSITY OF WASHINGTON · PI GORDON, SHARONA E, ZAGOTTA, WILLIAM N · 2012 to 2015
$1.5M
Electrophysiology-Optical Workstation for Ion Channel BiophysicsS10RR025429 · NCRR · UNIVERSITY OF WASHINGTON · PI GORDON, SHARONA E · 2009 to 2009
$499k
NCRR NIH HHS S10 RR025429NEI NIH HHS R01 EY013007NEI NIH HHS R01 EY017564NEI NIH HHS R01EY017564NIGMS NIH HHS R01 GM100718NIGMS NIH HHS R01GM100718
6 · The paper itself

Abstract

Phosphoinositides are vital for many cellular signaling processes, and therefore a number of approaches to manipulating phosphoinositide levels in cells or excised patches of cell membranes have been developed. Among the most common is the use of "short-chain" phosphoinositides, usually dioctanoyl phosphoinositol phosphates. We use isothermal titration calorimetry to determine partitioning of the most abundant phosphoinositol phosphates, PI(4)P and PI(4,5)P2 into models of the intracellular and extracellular facing leaflets of neuronal plasma membranes. We show that phosphoinositide mole fractions in the lipid membrane reach physiological levels at equilibrium with reasonable solution concentrations. Finally we explore the consequences of our results for cellular electrophysiology. In particular, we find that TRPV1 is more selective for PI(4,5)P2 than PI(4)P and activated by extremely low membrane mole fractions of PIPs. We conclude by discussing how the logic of our work extends to other experiments with short-chain phosphoinositides. For delayed rectifier K(+) channels, consideration of the membrane mole fraction of PI(4,5)P2 lipids with different acyl chain lengths suggests a different mechanism for PI(4,5)P2 regulation than previously proposed. Inward rectifier K(+) channels apparent lack of selectivity for certain short-chain PIPs may require reinterpretation in view of the PIPs different membrane partitioning.

Indexed as

Models, BiologicalCell MembraneHEK293 CellsHumansLiposomesPhosphatidylinositol PhosphatesShab Potassium ChannelsTRPV Cation ChannelsLiposomesPhosphatidylinositol PhosphatesShab Potassium ChannelsTRPV Cation Channels

Identifiers

PMID24314079
PMCPMC3853087
OpenAlexW2021566546

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.