Evidence map›Paper›PMID 15533917›Full record

ArticleBiophysical journal2005

Functional characterization of mammalian inositol 1,4,5-trisphosphate receptor isoforms.

Huiping Tu, Zhengnan Wang, Elena Nosyreva, Humbert De Smedt, Ilya Bezprozvanny

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Biophysical journal, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 13% 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

69 citing papers in PubMed, 1 synthesis or guideline pooled it, 128 citations in OpenAlex.

  1. Calcium and arrhythmogenesis.Physiological reviews · 2007
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  6. The signal that stimulates mammalian embryo development.Frontiers in cell and developmental biology · 2024
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  7. Sperm-Induced CaCells · 2023
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  10. Jaw1/LRMP increases CaScientific reports · 2022
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  13. The Ion Channel and GPCR Toolkit of Brain Capillary Pericytes.Frontiers in cellular neuroscience · 2020
    Review
  14. Review
  15. Review
  16. Spatial-temporal patterning of CaSeminars in cell & developmental biology · 2019
    Review
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  19. All three IPScience signaling · 2018
    Article
  20. Article

9 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 2 countries.

Huiping TuDepartment of Physiology, University of Texas Southwestern Medical Center at Dallas, Dallas, Texas 75390, USA.
Zhengnan Wang
Elena Nosyreva
Humbert De Smedt
Ilya Bezprozvanny
The University of Texas Southwestern Medical Center · USKU Leuven · BE

Funding

STRUCTURE/FUNCTION OF INOSITOL TRISPHOSPHATE RECEPTORR01NS038082 · NINDS · UT SOUTHWESTERN MEDICAL CENTER · PI BEZPROZVANNY, ILYA B · 1999 to 2009
$2.6M
NINDS NIH HHS R01 NS038082NINDS NIH HHS R01 NS38082
6 · The paper itself

Abstract

Inositol 1,4,5-trisphosphate receptors (InsP3R) play a key role in intracellular calcium (Ca2+) signaling. Three mammalian InsP3R isoforms--InsP3R type 1 (InsP3R1), InsP3R type 2 (InsP3R2), and InsP3R type 3 (InsP3R3) are expressed in mammals, but the functional differences between the three mammalian InsP3R isoforms are poorly understood. Here we compared single-channel behavior of the recombinant rat InsP3R1, InsP3R2, and InsP3R3 expressed in Sf9 cells, reconstituted into planar lipid bilayers and recorded with 50 mM Ba2+ as a current carrier. We found that: 1), for all three mammalian InsP3R isoforms the size of the unitary current is 1.9 pA and single-channel conductance is 74-80 pS; 2), in optimal recording conditions the maximal single-channel open probability for all three mammalian InsP3R isoforms is in the range 30-40%; 3), in optimal recording conditions the mean open dwell time for all three mammalian InsP3R isoforms is 7-8 ms, the mean closed dwell time is approximately 10 ms; 4), InsP3R2 has the highest apparent affinity for InsP(3) (0.10 microM), followed by InsP3R1 (0.27 microM), and then by InsP3R3 (0.40 microM); 5), InsP3R1 has a high-affinity (0.13 mM) ATP modulatory site, InsP3R2 gating is ATP independent, and InsP3R3 has a low-affinity (2 mM) ATP modulatory site; 6), ATP modulates InsP3R1 gating in a noncooperative manner (n(Hill) = 1.3); 7), ATP modulates InsP3R3 gating in a highly cooperative manner (n(Hill) = 4.1). Obtained results provide novel information about functional properties of mammalian InsP3R isoforms.

Indexed as

Ion Channel GatingMembrane PotentialsAdenosine TriphosphateAnimalsElectric ConductivityInositol 1,4,5-TrisphosphateKineticsLipid BilayersProtein IsoformsRatsRecombinant ProteinsStructure-Activity RelationshipAdenosine TriphosphateInositol 1,4,5-TrisphosphateLipid BilayersProtein IsoformsRecombinant Proteins

Identifiers

PMID15533917
PMCPMC1305111
OpenAlexW2118075049

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.