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Last Updated: 27/02/2023

Defining the functional role of a novel Plasmodium falciparum protein domain involved in liquid-liquid phase separation

Objectives

To uncover the functional role for a unique, previously uncharacterized P. falciparum protein domain.

Specific objectives:

  1. To characterize this domain by studying LLPS in vivo using a fluorescent reporter assay and directly in P. falciparum parasites.
  2. To determine in vitro protein interaction partners via protein pulldown assays and mass spectrometry leading to creation of transgenic parasites.
  3. To study the in vivo effect of modifications to this domain using CRISPR/Cas9.
Principal Institution

Karolinska Institute (KI), Sweden

Principal Investigators / Focal Persons

Philippa Reutersward Waldner

Rationale and Abstract

Malaria constitutes an enormous global health burden, and there is an urgent need to identify new targets for antimalarial therapy to eradicate this parasitic disease. In the malaria parasite, P. falciparum, transcriptional regulation is fundamental to parasite development. Apicomplexan Apetala 2 (ApiAP2) proteins are the main group of transcription factors regulating the malaria parasite lifecycle, acting as developmental switches between parasite life stages. Nine ApiAP2 proteins contain a highly conserved Apicomplexan-specific domain of unknown function, the ACDC domain. We have found that this novel domain may act in oligomerization to drive the formation of cellular liquid condensates by Liquid-Liquid phase separation (LLPS). These studies will provide the first mechanistic explanation for LLPS in malaria parasites.

Thematic Categories

Enabling Technologies & Assays

Date

Jan 2021 — Dec 2023

Total Project Funding

$346,000

Funding Details
Swedish Research Council (SRC), Sweden

Grant number: 2020-06500_VR
SEK 3.15 Million
Project Site

Sweden

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