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The Plasmodium circumsporozoite protein is proteolytically processed during cell invasion

The circumsporozoite protein (CSP) is the major surface protein of Plasmodium sporozoites, the infective stage of malaria. Although CSP has been extensively studied as a malaria vaccine candidate, little is known about its structure. Here, we show that CSP is proteolytically cleaved by a papain fami...

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Autores principales: Coppi, Alida, Pinzon-Ortiz, Consuelo, Hutter, Christina, Sinnis, Photini
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1995445/
https://www.ncbi.nlm.nih.gov/pubmed/15630135
http://dx.doi.org/10.1084/jem.20040989
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author Coppi, Alida
Pinzon-Ortiz, Consuelo
Hutter, Christina
Sinnis, Photini
author_facet Coppi, Alida
Pinzon-Ortiz, Consuelo
Hutter, Christina
Sinnis, Photini
author_sort Coppi, Alida
collection PubMed
description The circumsporozoite protein (CSP) is the major surface protein of Plasmodium sporozoites, the infective stage of malaria. Although CSP has been extensively studied as a malaria vaccine candidate, little is known about its structure. Here, we show that CSP is proteolytically cleaved by a papain family cysteine protease of parasite origin. Our data suggest that the highly conserved region I, found just before the repeat region, contains the cleavage site. Cleavage occurs on the sporozoite surface when parasites contact target cells. Inhibitors of CSP processing inhibit cell invasion in vitro, and treatment of mice with E-64, a highly specific cysteine protease inhibitor, completely inhibits sporozoite infectivity in vivo.
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spelling pubmed-19954452008-03-11 The Plasmodium circumsporozoite protein is proteolytically processed during cell invasion Coppi, Alida Pinzon-Ortiz, Consuelo Hutter, Christina Sinnis, Photini J Exp Med Brief Definitive Report The circumsporozoite protein (CSP) is the major surface protein of Plasmodium sporozoites, the infective stage of malaria. Although CSP has been extensively studied as a malaria vaccine candidate, little is known about its structure. Here, we show that CSP is proteolytically cleaved by a papain family cysteine protease of parasite origin. Our data suggest that the highly conserved region I, found just before the repeat region, contains the cleavage site. Cleavage occurs on the sporozoite surface when parasites contact target cells. Inhibitors of CSP processing inhibit cell invasion in vitro, and treatment of mice with E-64, a highly specific cysteine protease inhibitor, completely inhibits sporozoite infectivity in vivo. The Rockefeller University Press 2005-01-03 /pmc/articles/PMC1995445/ /pubmed/15630135 http://dx.doi.org/10.1084/jem.20040989 Text en Copyright © 2005, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Brief Definitive Report
Coppi, Alida
Pinzon-Ortiz, Consuelo
Hutter, Christina
Sinnis, Photini
The Plasmodium circumsporozoite protein is proteolytically processed during cell invasion
title The Plasmodium circumsporozoite protein is proteolytically processed during cell invasion
title_full The Plasmodium circumsporozoite protein is proteolytically processed during cell invasion
title_fullStr The Plasmodium circumsporozoite protein is proteolytically processed during cell invasion
title_full_unstemmed The Plasmodium circumsporozoite protein is proteolytically processed during cell invasion
title_short The Plasmodium circumsporozoite protein is proteolytically processed during cell invasion
title_sort plasmodium circumsporozoite protein is proteolytically processed during cell invasion
topic Brief Definitive Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1995445/
https://www.ncbi.nlm.nih.gov/pubmed/15630135
http://dx.doi.org/10.1084/jem.20040989
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