Evidence map›Paper›PMID 32736136›Full record

ArticleJournal of proteomics2020

Plasmodium berghei LAPs form an extended protein complex that facilitates crystalloid targeting and biogenesis.

Annie Z Tremp, Sadia Saeed, Vikram Sharma, Edwin Lasonder, Johannes T Dessens

Open access · hybridAbstract read
In one paragraph

Article in Journal of proteomics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

12 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. A pleckstrin homology domain protein is involved in crystalloid formation inFrontiers in cellular and infection microbiology · 2026
    Article
  3. The Crystal Structure ofBiochemistry · 2025
    Article
  4. Open biology · 2024
    Article
  5. The molecular mechanisms driving Plasmodium cell division.Biochemical Society transactions · 2024
    Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Microbiology spectrum · 2022
    Article
  11. mBio · 2022
    Article
  12. 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

5 authors at 3 institutions in 1 country.

Annie Z TrempDepartment of Infection Biology, Faculty of Infectious and Tropical Diseases, London School of Hygiene & Tropical Medicine, Keppel Street, London, WC1E 7HT, UK.
Sadia SaeedDepartment of Infection Biology, Faculty of Infectious and Tropical Diseases, London School of Hygiene & Tropical Medicine, Keppel Street, London, WC1E 7HT, UK.
Vikram SharmaSchool of Biomedical Sciences, Faculty of Health, Plymouth University, Drake Circus, Plymouth, PL4 8AA, UK.
Edwin LasonderSchool of Biomedical Sciences, Faculty of Health, Plymouth University, Drake Circus, Plymouth, PL4 8AA, UK; Department of Applied Sciences, Faculty of Life and Health Sciences, Northumbria University, Newcastle-Upon-Tyne, NE1 8ST, UK.
Johannes T DessensDepartment of Infection Biology, Faculty of Infectious and Tropical Diseases, London School of Hygiene & Tropical Medicine, Keppel Street, London, WC1E 7HT, UK. Electronic address: Johannes.Dessens@lshtm.ac.uk.
London School of Hygiene & Tropical Medicine · GBNorthumbria University · GBUniversity of Plymouth · GB

Funding

Biotechnology and Biological Sciences Research Council BB/M001598Medical Research Council MR/P021611Medical Research Council MR/P021611/1Wellcome Trust 088449
6 · The paper itself

Abstract

Passage of malaria parasites through mosquitoes involves multiple developmental transitions, from gametocytes that are ingested with the blood meal, through to sporozoites that are transmitted by insect bite to the host. During the transformation from gametocyte to oocyst, the parasite forms a unique transient organelle named the crystalloid, which is involved in sporozoite formation. In Plasmodium berghei, a complex of six LCCL domain-containing proteins (LAPs) reside in the crystalloid and are required for its biogenesis. However, little else is known about the molecular mechanisms that underlie the crystalloid's role in sporogony. In this study, we have used transgenic parasites stably expressing LAP3 fused to GFP, combined with GFP affinity pulldown and high accuracy mass spectrometry, to identify an extended LAP interactome of some fifty proteins. We show that many of these are targeted to the crystalloid, including members of two protein families with CPW-WPC and pleckstrin homology-like domains, respectively. Our findings indicate that the LAPs are part of an intricate protein complex, the formation of which facilitates both crystalloid targeting and biogenesis. SIGNIFICANCE: Reducing malaria parasite transmission by mosquitoes is a key component of malaria eradication and control strategies. This study sheds important new light on the molecular composition of the crystalloid, an enigmatic parasite organelle that is essential for sporozoite formation and transmission from the insect to the vertebrate host. Our findings provide new mechanistic insight into how proteins are delivered to the crystalloid, and indicate that the molecular mechanisms that underlie crystalloid function are complex, involving several protein families unique to Plasmodium and closely related organisms. The new crystalloid proteins identified will form a useful starting point for studies aimed at unravelling how the crystalloid organelle facilitates sporogony and transmission.

Indexed as

MalariaPlasmodium bergheiAnimalsCrystalloid SolutionsHumansOrganellesProtozoan ProteinsCrystalloid SolutionsProtozoan Proteins

Identifiers

PMID32736136
PMCPMC7487766
OpenAlexW3046205767

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.