Evidence map›Paper›PMID 19576251›Full record

ArticleMolecular and biochemical parasitology2009

Effects of calcium signaling on Plasmodium falciparum erythrocyte invasion and post-translational modification of gliding-associated protein 45 (PfGAP45).

Matthew L Jones, Chris Cottingham, Julian C Rayner

Abstract read
In one paragraph

Article in Molecular and biochemical parasitology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
4.3field-weighted citation impact, top 7% 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

26 citing papers in PubMed, 52 citations in OpenAlex.

  1. Article
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  7. Atlas ofeLife · 2023
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  8. Atlas ofbioRxiv : the preprint server for biology · 2023
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  9. Article
  10. Identification of basal complex protein that is essential for maturation of transmission-stage malaria parasites.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  11. Gliding motility ofProceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  12. Diverse Roles of TgMIC1/4/6 in theFrontiers in microbiology · 2021
    Review
  13. Article
  14. Article
  15. Pumilacidins from the Octocoral-AssociatedMolecules (Basel, Switzerland) · 2018
    Article
  16. Article
  17. Article
  18. Review
  19. InsP3 Signaling in Apicomplexan Parasites.Current topics in medicinal chemistry · 2017
    Review
  20. 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

3 authors at 2 institutions in 2 countries.

Matthew L JonesDepartment of Medicine, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Chris Cottingham
Julian C Rayner
University of Alabama at Birmingham · USWellcome Sanger Institute · GB

Funding

Agents of International Health &Bioterrorism ConcernT32AI055438 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI NOVAK, ROBERT J · 2003 to 2007
$1.4M
NIAID NIH HHS T32 AI055438
6 · The paper itself

Abstract

Plasmodium falciparum erythrocyte invasion is powered by an actin/myosin motor complex that is linked both to the tight junction and to the merozoite cytoskeleton through the Inner Membrane Complex (IMC). The IMC association of the myosin motor, PfMyoA, is maintained by its association with three proteins: PfMTIP, a myosin light chain, PfGAP45, an IMC peripheral membrane protein, and PfGAP50, an integral membrane protein of the IMC. This protein complex is referred to as the glideosome, and given its central role in erythrocyte invasion, this complex is likely the target of several specific regulatory effectors that ensure it is properly localized, assembled, and activated as the merozoite prepares to invade its target cell. However, little is known about how erythrocyte invasion as a whole is regulated, or about how or whether that regulation impacts the glideosome. Here we show that P. falciparum erythrocyte invasion is regulated by the release of intracellular calcium via the cyclic-ADP Ribose (cADPR) pathway, but that inhibition of cADPR-mediated calcium release does not affect PfGAP45 phosphorylation or glideosome association. By contrast, the serine/threonine kinase inhibitor, staurosporine, affects both PfGAP45 isoform distribution and the integrity of the glideosome complex. This data identifies specific regulatory elements involved in controlling P. falciparum erythrocyte invasion and reveals that the assembly status of the merozoite glideosome, which is central to erythrocyte invasion, is surprisingly dynamic.

Indexed as

Calcium SignalingGene Expression RegulationAnimalsErythrocytesMembrane ProteinsPhosphorylationPlasmodium falciparumProtein BindingProtein IsoformsProtein Processing, Post-Translationalglideosome-associated protein 45, Plasmodium falciparumMembrane ProteinsProtein Isoforms

Identifiers

PMID19576251
PMCPMC2754074
OpenAlexW2002279886

What OpenQuestion holds

Textmetadata
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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.