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A druggable secretory protein maturase of Toxoplasma essential for invasion and egress
Micronemes and rhoptries are specialized secretory organelles that deploy their contents at the apical tip of apicomplexan parasites in a regulated manner. The secretory proteins participate in motility, invasion, and egress and are subjected to proteolytic maturation prior to organellar storage and...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5595437/ https://www.ncbi.nlm.nih.gov/pubmed/28898199 http://dx.doi.org/10.7554/eLife.27480 |
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author | Dogga, Sunil Kumar Mukherjee, Budhaditya Jacot, Damien Kockmann, Tobias Molino, Luca Hammoudi, Pierre-Mehdi Hartkoorn, Ruben C Hehl, Adrian B Soldati-Favre, Dominique |
author_facet | Dogga, Sunil Kumar Mukherjee, Budhaditya Jacot, Damien Kockmann, Tobias Molino, Luca Hammoudi, Pierre-Mehdi Hartkoorn, Ruben C Hehl, Adrian B Soldati-Favre, Dominique |
author_sort | Dogga, Sunil Kumar |
collection | PubMed |
description | Micronemes and rhoptries are specialized secretory organelles that deploy their contents at the apical tip of apicomplexan parasites in a regulated manner. The secretory proteins participate in motility, invasion, and egress and are subjected to proteolytic maturation prior to organellar storage and discharge. Here we establish that Toxoplasma gondii aspartyl protease 3 (ASP3) resides in the endosomal-like compartment and is crucially associated to rhoptry discharge during invasion and to host cell plasma membrane lysis during egress. A comparison of the N-terminome, by terminal amine isotopic labelling of substrates between wild type and ASP3 depleted parasites identified microneme and rhoptry proteins as repertoire of ASP3 substrates. The role of ASP3 as a maturase for previously described and newly identified secretory proteins is confirmed in vivo and in vitro. An antimalarial compound based on a hydroxyethylamine scaffold interrupts the lytic cycle of T. gondii at submicromolar concentration by targeting ASP3. |
format | Online Article Text |
id | pubmed-5595437 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-55954372017-09-18 A druggable secretory protein maturase of Toxoplasma essential for invasion and egress Dogga, Sunil Kumar Mukherjee, Budhaditya Jacot, Damien Kockmann, Tobias Molino, Luca Hammoudi, Pierre-Mehdi Hartkoorn, Ruben C Hehl, Adrian B Soldati-Favre, Dominique eLife Microbiology and Infectious Disease Micronemes and rhoptries are specialized secretory organelles that deploy their contents at the apical tip of apicomplexan parasites in a regulated manner. The secretory proteins participate in motility, invasion, and egress and are subjected to proteolytic maturation prior to organellar storage and discharge. Here we establish that Toxoplasma gondii aspartyl protease 3 (ASP3) resides in the endosomal-like compartment and is crucially associated to rhoptry discharge during invasion and to host cell plasma membrane lysis during egress. A comparison of the N-terminome, by terminal amine isotopic labelling of substrates between wild type and ASP3 depleted parasites identified microneme and rhoptry proteins as repertoire of ASP3 substrates. The role of ASP3 as a maturase for previously described and newly identified secretory proteins is confirmed in vivo and in vitro. An antimalarial compound based on a hydroxyethylamine scaffold interrupts the lytic cycle of T. gondii at submicromolar concentration by targeting ASP3. eLife Sciences Publications, Ltd 2017-09-12 /pmc/articles/PMC5595437/ /pubmed/28898199 http://dx.doi.org/10.7554/eLife.27480 Text en © 2017, Dogga et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Microbiology and Infectious Disease Dogga, Sunil Kumar Mukherjee, Budhaditya Jacot, Damien Kockmann, Tobias Molino, Luca Hammoudi, Pierre-Mehdi Hartkoorn, Ruben C Hehl, Adrian B Soldati-Favre, Dominique A druggable secretory protein maturase of Toxoplasma essential for invasion and egress |
title | A druggable secretory protein maturase of Toxoplasma essential for invasion and egress |
title_full | A druggable secretory protein maturase of Toxoplasma essential for invasion and egress |
title_fullStr | A druggable secretory protein maturase of Toxoplasma essential for invasion and egress |
title_full_unstemmed | A druggable secretory protein maturase of Toxoplasma essential for invasion and egress |
title_short | A druggable secretory protein maturase of Toxoplasma essential for invasion and egress |
title_sort | druggable secretory protein maturase of toxoplasma essential for invasion and egress |
topic | Microbiology and Infectious Disease |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5595437/ https://www.ncbi.nlm.nih.gov/pubmed/28898199 http://dx.doi.org/10.7554/eLife.27480 |
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