Ca 2+ signals critical for egress and gametogenesis in malaria parasites depend on a multipass membrane protein that interacts with PKG

Author:

Balestra Aurélia C.1ORCID,Koussis Konstantinos2ORCID,Klages Natacha1,Howell Steven A.3,Flynn Helen R.3ORCID,Bantscheff Marcus4ORCID,Pasquarello Carla5,Perrin Abigail J.2ORCID,Brusini Lorenzo1ORCID,Arboit Patrizia5,Sanz Olalla6ORCID,Castaño Laura Peces-Barba2ORCID,Withers-Martinez Chrislaine2ORCID,Hainard Alexandre5,Ghidelli-Disse Sonja4ORCID,Snijders Ambrosius P.3ORCID,Baker David A.7ORCID,Blackman Michael J.27ORCID,Brochet Mathieu1ORCID

Affiliation:

1. Department of Microbiology and Molecular Medicine, Faculty of Medicine, University of Geneva, CH-1211 Geneva, Switzerland.

2. Malaria Biochemistry Laboratory, The Francis Crick Institute, London NW1 1AT, UK.

3. Mass Spectrometry Proteomics Platform, The Francis Crick Institute, London, UK.

4. Cellzome GmbH, Molecular Discovery Research, GlaxoSmithKline, 69117 Heidelberg, Germany.

5. Proteomics Core Facility, Faculty of Medicine, University of Geneva, CH-1211 Geneva, Switzerland.

6. Diseases of the Developing World Global Health Pharma Unit, GlaxoSmithKline, 28760 Tres Cantos, Spain.

7. Faculty of Infectious and Tropical Diseases, London School of Hygiene & Tropical Medicine, London WC1E 7HT, UK.

Abstract

A membrane protein interacts with PKG and regulates calcium signals at multiple lifecycle stages in malaria parasites.

Funder

Novartis Foundation

Wellcome

Medical Research Council

Swiss National Science Foundation

Fondation privée des Hôpitaux Universitaires de Genève

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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