Evidence map›Paper›PMID 33974939›Full record

ArticleMolecular and biochemical parasitology2021

Identification and characterisation of a phospholipid scramblase in the malaria parasite Plasmodium falciparum.

Silvia Haase, Melanie Condron, David Miller, Dounia Cherkaoui, Sarah Jordan, Jacqueline M Gulbis, Jake Baum

Open access · hybridAbstract read
In one paragraph

Article in Molecular and biochemical parasitology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

11 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
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  5. TargetingVaccines · 2024
    Review
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  7. Updated List of Transport Proteins inFrontiers in cellular and infection microbiology · 2022
    Review
  8. Article
  9. Article
  10. Review
  11. 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

7 authors at 3 institutions in 2 countries.

Silvia HaaseDepartment of Life Sciences, Imperial College London, Sir Alexander Fleming Building, Exhibition Road, South Kensington, London, UK. Electronic address: silvia.haase@crick.ac.uk.
Melanie CondronDivision of Infection and Immunity, The Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.
David MillerDivision of Structural Biology, The Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.
Dounia CherkaouiDepartment of Life Sciences, Imperial College London, Sir Alexander Fleming Building, Exhibition Road, South Kensington, London, UK.
Sarah JordanDepartment of Life Sciences, Imperial College London, Sir Alexander Fleming Building, Exhibition Road, South Kensington, London, UK.
Jacqueline M GulbisDivision of Structural Biology, The Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia; Department of Medical Biology, The University of Melbourne, Melbourne, Victoria, Australia.
Jake BaumDepartment of Life Sciences, Imperial College London, Sir Alexander Fleming Building, Exhibition Road, South Kensington, London, UK. Electronic address: jake.baum@imperial.ac.uk.
Imperial College London · GBWalter and Eliza Hall Institute of Medical Research · AUThe University of Melbourne · AU

Funding

Wellcome TrustWellcome Trust 100993/Z/13/Z
6 · The paper itself

Abstract

Recent studies highlight the emerging role of lipids as important messengers in malaria parasite biology. In an attempt to identify interacting proteins and regulators of these dynamic and versatile molecules, we hypothesised the involvement of phospholipid translocases and their substrates in the infection of the host erythrocyte by the malaria parasite Plasmodium spp. Here, using a data base searching approach of the Plasmodium Genomics Resources (www.plasmodb.org), we have identified a putative phospholipid (PL) scramblase in P. falciparum (PfPLSCR) that is conserved across the genus and in closely related unicellular algae. By reconstituting recombinant PfPLSCR into liposomes, we demonstrate metal ion dependent PL translocase activity and substrate preference, confirming PfPLSCR as a bona fide scramblase. We show that PfPLSCR is expressed during asexual and sexual parasite development, localising to different membranous compartments of the parasite throughout the intra-erythrocytic life cycle. Two different gene knockout approaches, however, suggest that PfPLSCR is not essential for erythrocyte invasion and asexual parasite development, pointing towards a possible role in other stages of the parasite life cycle.

Indexed as

Amino Acid SequenceApicomplexaConserved SequenceErythrocytesGene Expression Regulation, EnzymologicHumansLiposomesMicroorganisms, Genetically-ModifiedPhospholipid Transfer ProteinsPlasmodium falciparumProtozoan ProteinsRecombinant ProteinsLiposomesPhospholipid Transfer ProteinsPLSCR1 protein, humanProtozoan ProteinsRecombinant ProteinsGametocytesInvasionLiposomesMalariaPhospholipid scramblasePlasmodium falciparum

Identifiers

PMID33974939
PMCPMC8202325
OpenAlexW3160855223

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.