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Ribosome-Inactivating Proteins: From Plant Defense to Tumor Attack

Ribosome-inactivating proteins (RIPs) are EC3.2.32.22 N-glycosidases that recognize a universally conserved stem-loop structure in 23S/25S/28S rRNA, depurinating a single adenine (A4324 in rat) and irreversibly blocking protein translation, leading finally to cell death of intoxicated mammalian cell...

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Detalles Bibliográficos
Autores principales: de Virgilio, Maddalena, Lombardi, Alessio, Caliandro, Rocco, Fabbrini, Maria Serena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3153179/
https://www.ncbi.nlm.nih.gov/pubmed/22069572
http://dx.doi.org/10.3390/toxins2112699
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author de Virgilio, Maddalena
Lombardi, Alessio
Caliandro, Rocco
Fabbrini, Maria Serena
author_facet de Virgilio, Maddalena
Lombardi, Alessio
Caliandro, Rocco
Fabbrini, Maria Serena
author_sort de Virgilio, Maddalena
collection PubMed
description Ribosome-inactivating proteins (RIPs) are EC3.2.32.22 N-glycosidases that recognize a universally conserved stem-loop structure in 23S/25S/28S rRNA, depurinating a single adenine (A4324 in rat) and irreversibly blocking protein translation, leading finally to cell death of intoxicated mammalian cells. Ricin, the plant RIP prototype that comprises a catalytic A subunit linked to a galactose-binding lectin B subunit to allow cell surface binding and toxin entry in most mammalian cells, shows a potency in the picomolar range. The most promising way to exploit plant RIPs as weapons against cancer cells is either by designing molecules in which the toxic domains are linked to selective tumor targeting domains or directly delivered as suicide genes for cancer gene therapy. Here, we will provide a comprehensive picture of plant RIPs and discuss successful designs and features of chimeric molecules having therapeutic potential.
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spelling pubmed-31531792011-11-08 Ribosome-Inactivating Proteins: From Plant Defense to Tumor Attack de Virgilio, Maddalena Lombardi, Alessio Caliandro, Rocco Fabbrini, Maria Serena Toxins (Basel) Review Ribosome-inactivating proteins (RIPs) are EC3.2.32.22 N-glycosidases that recognize a universally conserved stem-loop structure in 23S/25S/28S rRNA, depurinating a single adenine (A4324 in rat) and irreversibly blocking protein translation, leading finally to cell death of intoxicated mammalian cells. Ricin, the plant RIP prototype that comprises a catalytic A subunit linked to a galactose-binding lectin B subunit to allow cell surface binding and toxin entry in most mammalian cells, shows a potency in the picomolar range. The most promising way to exploit plant RIPs as weapons against cancer cells is either by designing molecules in which the toxic domains are linked to selective tumor targeting domains or directly delivered as suicide genes for cancer gene therapy. Here, we will provide a comprehensive picture of plant RIPs and discuss successful designs and features of chimeric molecules having therapeutic potential. MDPI 2010-11-10 /pmc/articles/PMC3153179/ /pubmed/22069572 http://dx.doi.org/10.3390/toxins2112699 Text en © 2010 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
de Virgilio, Maddalena
Lombardi, Alessio
Caliandro, Rocco
Fabbrini, Maria Serena
Ribosome-Inactivating Proteins: From Plant Defense to Tumor Attack
title Ribosome-Inactivating Proteins: From Plant Defense to Tumor Attack
title_full Ribosome-Inactivating Proteins: From Plant Defense to Tumor Attack
title_fullStr Ribosome-Inactivating Proteins: From Plant Defense to Tumor Attack
title_full_unstemmed Ribosome-Inactivating Proteins: From Plant Defense to Tumor Attack
title_short Ribosome-Inactivating Proteins: From Plant Defense to Tumor Attack
title_sort ribosome-inactivating proteins: from plant defense to tumor attack
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3153179/
https://www.ncbi.nlm.nih.gov/pubmed/22069572
http://dx.doi.org/10.3390/toxins2112699
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