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RhopH2 and RhopH3 export enables assembly of the RhopH complex on P. falciparum-infected erythrocyte membranes

RhopH complexes consists of Clag3, RhopH2 and RhopH3 and are essential for growth of Plasmodium falciparum inside infected erythrocytes. Proteins are released from rhoptry organelles during merozoite invasion and trafficked to the surface of infected erythrocytes and enable uptake of nutrients. Rhop...

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Autores principales: Pasternak, Michał, Verhoef, Julie M. J., Wong, Wilson, Triglia, Tony, Mlodzianoski, Michael J., Geoghegan, Niall, Evelyn, Cindy, Wardak, Ahmad Z., Rogers, Kelly, Cowman, Alan F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8989874/
https://www.ncbi.nlm.nih.gov/pubmed/35393572
http://dx.doi.org/10.1038/s42003-022-03290-3
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author Pasternak, Michał
Verhoef, Julie M. J.
Wong, Wilson
Triglia, Tony
Mlodzianoski, Michael J.
Geoghegan, Niall
Evelyn, Cindy
Wardak, Ahmad Z.
Rogers, Kelly
Cowman, Alan F.
author_facet Pasternak, Michał
Verhoef, Julie M. J.
Wong, Wilson
Triglia, Tony
Mlodzianoski, Michael J.
Geoghegan, Niall
Evelyn, Cindy
Wardak, Ahmad Z.
Rogers, Kelly
Cowman, Alan F.
author_sort Pasternak, Michał
collection PubMed
description RhopH complexes consists of Clag3, RhopH2 and RhopH3 and are essential for growth of Plasmodium falciparum inside infected erythrocytes. Proteins are released from rhoptry organelles during merozoite invasion and trafficked to the surface of infected erythrocytes and enable uptake of nutrients. RhopH3, unlike other RhopH proteins, is required for parasite invasion, suggesting some cellular processes RhopH proteins function as single players rather than a complex. We show the RhopH complex has not formed during merozoite invasion. Clag3 is directly released into the host cell cytoplasm, whilst RhopH2 and RhopH3 are released into the nascent parasitophorous vacuole. Export of RhopH2 and RhopH3 from the parasitophorous vacuole into the infected erythrocyte cytoplasm enables assembly of Clag3/RhopH2/RhopH3 complexes and incorporation into the host cell membrane concomitant with activation of nutrient uptake. This suggests compartmentalisation prevents premature channel assembly before intact complex is assembled at the host cell membrane.
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spelling pubmed-89898742022-04-22 RhopH2 and RhopH3 export enables assembly of the RhopH complex on P. falciparum-infected erythrocyte membranes Pasternak, Michał Verhoef, Julie M. J. Wong, Wilson Triglia, Tony Mlodzianoski, Michael J. Geoghegan, Niall Evelyn, Cindy Wardak, Ahmad Z. Rogers, Kelly Cowman, Alan F. Commun Biol Article RhopH complexes consists of Clag3, RhopH2 and RhopH3 and are essential for growth of Plasmodium falciparum inside infected erythrocytes. Proteins are released from rhoptry organelles during merozoite invasion and trafficked to the surface of infected erythrocytes and enable uptake of nutrients. RhopH3, unlike other RhopH proteins, is required for parasite invasion, suggesting some cellular processes RhopH proteins function as single players rather than a complex. We show the RhopH complex has not formed during merozoite invasion. Clag3 is directly released into the host cell cytoplasm, whilst RhopH2 and RhopH3 are released into the nascent parasitophorous vacuole. Export of RhopH2 and RhopH3 from the parasitophorous vacuole into the infected erythrocyte cytoplasm enables assembly of Clag3/RhopH2/RhopH3 complexes and incorporation into the host cell membrane concomitant with activation of nutrient uptake. This suggests compartmentalisation prevents premature channel assembly before intact complex is assembled at the host cell membrane. Nature Publishing Group UK 2022-04-07 /pmc/articles/PMC8989874/ /pubmed/35393572 http://dx.doi.org/10.1038/s42003-022-03290-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Pasternak, Michał
Verhoef, Julie M. J.
Wong, Wilson
Triglia, Tony
Mlodzianoski, Michael J.
Geoghegan, Niall
Evelyn, Cindy
Wardak, Ahmad Z.
Rogers, Kelly
Cowman, Alan F.
RhopH2 and RhopH3 export enables assembly of the RhopH complex on P. falciparum-infected erythrocyte membranes
title RhopH2 and RhopH3 export enables assembly of the RhopH complex on P. falciparum-infected erythrocyte membranes
title_full RhopH2 and RhopH3 export enables assembly of the RhopH complex on P. falciparum-infected erythrocyte membranes
title_fullStr RhopH2 and RhopH3 export enables assembly of the RhopH complex on P. falciparum-infected erythrocyte membranes
title_full_unstemmed RhopH2 and RhopH3 export enables assembly of the RhopH complex on P. falciparum-infected erythrocyte membranes
title_short RhopH2 and RhopH3 export enables assembly of the RhopH complex on P. falciparum-infected erythrocyte membranes
title_sort rhoph2 and rhoph3 export enables assembly of the rhoph complex on p. falciparum-infected erythrocyte membranes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8989874/
https://www.ncbi.nlm.nih.gov/pubmed/35393572
http://dx.doi.org/10.1038/s42003-022-03290-3
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