Evidence map›Paper›PMID 39264987›Full record

ArticlePLoS biology2024

Alveolin proteins in the Toxoplasma inner membrane complex form a highly interconnected structure that maintains parasite shape and replication.

Peter S Back, Vignesh Senthilkumar, Charles P Choi, Justin J Quan, Qing Lou, Anne K Snyder, Andrew M Ly, Justin G Lau, Z Hong Zhou, Gary E Ward and 1 more

Abstract read
In one paragraph

Article in PLoS biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. mBio · 2025
    Article
  5. Molecular features of Myosin F adapted for driving actin flows inbioRxiv : the preprint server for biology · 2025
    Article
  6. 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

11 authors.

Peter S BackMolecular Biology Institute, University of California, Los Angeles, Los Angeles, California, United States of America.
Vignesh SenthilkumarDepartment of Microbiology, Immunology, and Molecular Genetics, University of California, Los Angeles, Los Angeles, California, United States of America.
Charles P ChoiDepartment of Microbiology, Immunology, and Molecular Genetics, University of California, Los Angeles, Los Angeles, California, United States of America.
Justin J QuanDepartment of Microbiology, Immunology, and Molecular Genetics, University of California, Los Angeles, Los Angeles, California, United States of America.
Qing LouDepartment of Materials Science and Engineering, University of California, Los Angeles, Los Angeles, California, United States of America.
Anne K SnyderDepartment of Microbiology and Molecular Genetics, Larner College of Medicine, University of Vermont, Burlington, Vermont, United States of America.
Andrew M LyDepartment of Microbiology, Immunology, and Molecular Genetics, University of California, Los Angeles, Los Angeles, California, United States of America.
Justin G LauDepartment of Microbiology, Immunology, and Molecular Genetics, University of California, Los Angeles, Los Angeles, California, United States of America.
Z Hong ZhouMolecular Biology Institute, University of California, Los Angeles, Los Angeles, California, United States of America.
Gary E WardDepartment of Microbiology and Molecular Genetics, Larner College of Medicine, University of Vermont, Burlington, Vermont, United States of America.
Peter J BradleyMolecular Biology Institute, University of California, Los Angeles, Los Angeles, California, United States of America.ORCID 0000-0002-8481-0638

Funding

UCLA NIGMS T32 Program AssessmentT32GM007185 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI TORRES, JORGE · 1985 to 2020
$21.7M
High-Resolution CryoEM Reconstruction of Large ComplexesR01GM071940 · NIGMS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI ZHOU, Z HONG · 2006 to 2025
$5.0M
Functional Analysis of Novel Components of the Toxoplasma Inner Membrane ComplexR01AI123360 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Peter John Bradley · 2017 to 2026
$3.8M
Multiscale analysis of MyosinA-based motility in Toxoplasma gondiiR01AI139201 · NIAID · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI WARD, GARY E · 2019 to 2023
$2.8M
Vermont Immunology/Infectious Diseases Training GrantT32AI055402 · NIAID · UNIVERSITY OF VERMONT &ST AGRIC COLLEGE · PI GARY E WARD · 2005 to 2026
$2.7M
Mapping the directionality of forces generated by T. gondii tachyzoites moving in 3DR21AI137767 · NIAID · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI WARD, GARY E · 2018 to 2019
$411k
NIAID NIH HHS R01 AI123360NIAID NIH HHS R01 AI139201NIAID NIH HHS R21 AI137767NIAID NIH HHS T32 AI055402NIGMS NIH HHS R01 GM071940NIGMS NIH HHS T32 GM007185
6 · The paper itself

Abstract

Apicomplexan parasites possess several specialized structures to invade their host cells and replicate successfully. One of these is the inner membrane complex (IMC), a peripheral membrane-cytoskeletal system underneath the plasma membrane. It is composed of a series of flattened, membrane-bound vesicles and a cytoskeletal subpellicular network (SPN) comprised of intermediate filament-like proteins called alveolins. While the alveolin proteins are conserved throughout the Apicomplexa and the broader Alveolata, their precise functions and interactions remain poorly understood. Here, we describe the function of one of these alveolin proteins in Toxoplasma, IMC6. Disruption of IMC6 resulted in striking morphological defects that led to aberrant invasion and replication but surprisingly minor effects on motility. Deletion analyses revealed that the alveolin domain alone is largely sufficient to restore localization and partially sufficient for function. As this highlights the importance of the IMC6 alveolin domain, we implemented unnatural amino acid photoreactive crosslinking to the alveolin domain and identified multiple binding interfaces between IMC6 and 2 other cytoskeletal IMC proteins-IMC3 and ILP1. This provides direct evidence of protein-protein interactions in the alveolin domain and supports the long-held hypothesis that the alveolin domain is responsible for filament formation. Collectively, our study features the conserved alveolin proteins as critical components that maintain the parasite's structural integrity and highlights the alveolin domain as a key mediator of SPN architecture.

Indexed as

Cell MembraneProtozoan ProteinsToxoplasmaAnimalsCytoskeletonHumansProtein BindingProtein DomainsProtozoan Proteins

Identifiers

PMID39264987
PMCPMC11421793

What Socratic 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 Socratic graph.