Affinage · Toxoplasma gondii

ICMAP2

intraconoidal microtubule-associated protein ICMAP2 · UniProt S8F0H4

Annotated
2026-09-08
1 papers in source corpus 1 papers cited in narrative 1 extracted findings

Mechanistic narrative

Synthesis pass · prose summary of the discoveries below

ICMAP2 is an intraconoidal microtubule-associated protein in Toxoplasma gondii required to maintain the integrity of the intraconoidal microtubules (ICMTs) and their attachment to the conoid (PMID:38191574). Conditional depletion of ICMAP2 causes the ICMTs to dissociate and detach from the conoid, with concomitant dispersion of microtubule-associated vesicles and rhoptries, establishing that ICMAP2 scaffolds the positioning of these organelles for sustained, iterative rhoptry discharge during invasion (PMID:38191574). Beyond this single loss-of-function characterization, no further molecular detail — including direct binding partners, structural basis of ICMT association, or biochemical activity — has been characterized in the available corpus.

Mechanistic history

Synthesis pass · year-by-year structured walk · 1 step
  1. 2024 High

    It was unknown what maintains intraconoidal microtubule cohesion and anchors them to the conoid; conditional depletion showed ICMAP2 is required for ICMT integrity and for scaffolding the positioning of microtubule-associated vesicles and rhoptries, establishing its role in enabling iterative rhoptry discharge.

    Evidence Conditional knockdown of ICMAP2 with ultrastructural and fluorescence imaging of ICMT organization, conoid attachment, and rhoptry/MV localization in Toxoplasma gondii

    PMID:38191574

    Open questions at the time
    • No direct binding partners or molecular basis of ICMAP2-ICMT association identified
    • No structural model of how ICMAP2 tethers ICMTs to the conoid
    • Mechanism linking ICMT integrity to rhoptry discharge not resolved biochemically

Open questions

Synthesis pass · forward-looking unresolved questions
  • The molecular partners, structural basis of microtubule binding, and biochemical activity of ICMAP2 remain undefined.
  • No interactome or reciprocal binding validation for ICMAP2
  • No domain-level or structural characterization
  • No mechanism for how ICMAP2 loss propagates to rhoptry mispositioning

Mechanism profile

Synthesis pass · controlled-vocabulary classification
No controlled-vocabulary terms were assigned to this entry.

Evidence

Reading pass · 1 per-paper finding extracted from the source corpus
Year Finding Method Journal Conf PMIDs
2024 Depletion of ICMAP2 causes dissociation of intraconoidal microtubules (ICMTs), their detachment from the conoid, and dispersion of microtubule-associated vesicles (MVs) and rhoptries, demonstrating that ICMAP2 is required for maintaining ICMT integrity and scaffolding rhoptry positioning for iterative discharge. Conditional depletion (knockdown) of ICMAP2 with ultrastructural and fluorescence imaging readouts of ICMT organization, conoid attachment, and rhoptry/MV localization Nature communications High 38191574

Source papers

Stage 0 corpus · 1 paper · ranked by NIH iCite citations
Year Title Journal Citations PMID
2024 Sustained rhoptry docking and discharge requires Toxoplasma gondii intraconoidal microtubule-associated proteins. Nature communications 16 38191574