Evidence map›Paper›PMID 17921221›Full record

ArticleBiophysical journal2008

Decoding of calcium oscillations by phosphorylation cycles: analytic results.

Carlos Salazar, Antonio Zaccaria Politi, Thomas Höfer

Abstract read
In one paragraph

Article in Biophysical journal, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing 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

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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

33 citing papers in PubMed.

  1. Differential regulation of calcium-activated plant kinases in Arabidopsis thaliana.The Plant journal : for cell and molecular biology · 2025
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  5. Review
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  11. CaBiophysical journal · 2020
    Article
  12. IPiScience · 2020
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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

3 authors.

Carlos SalazarResearch Group Modeling of Biological Systems, German Cancer Research Center, Heidelberg, Germany. c.salazar@dkfz-heidelberg.de
Antonio Zaccaria Politi
Thomas Höfer

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Experimental studies have demonstrated that Ca(2+)-regulated proteins are sensitive to the frequency of Ca(2+) oscillations, and several mathematical models for specific proteins have provided insight into the mechanisms involved. Because of the large number of Ca(2+)-regulated proteins in signal transduction, metabolism and gene expression, it is desirable to establish in general terms which molecular properties shape the response to oscillatory Ca(2+) signals. Here we address this question by analyzing in detail a model of a prototypical Ca(2+)-decoding module, consisting of a target protein whose activity is controlled by a Ca(2+)-activated kinase and the counteracting phosphatase. We show that this module can decode the frequency of Ca(2+) oscillations, at constant average Ca(2+) signal, provided that the Ca(2+) spikes are narrow and the oscillation frequency is sufficiently low--of the order of the phosphatase rate constant or below. Moreover, Ca(2+) oscillations activate the target more efficiently than a constant signal when Ca(2+) is bound cooperatively and with low affinity. Thus, the rate constants and the Ca(2+) affinities of the target-modifying enzymes can be tuned in such a way that the module responds optimally to Ca(2+) spikes of a certain amplitude and frequency. Frequency sensitivity is further enhanced when the limited duration of the external stimulus driving Ca(2+) signaling is accounted for. Thus, our study identifies molecular parameters that may be involved in establishing the specificity of cellular responses downstream of Ca(2+) oscillations.

Indexed as

Models, BiologicalBiological ClocksCalciumCalcium SignalingComputer SimulationOscillometryPhosphorylationPhosphotransferasesCalciumPhosphotransferases

Identifiers

PMID17921221
PMCPMC2212700

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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.