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Ribosome Inactivating Proteins from Rosaceae
Ribosome-inactivating proteins (RIPs) are widespread among higher plants of different taxonomic orders. In this study, we report on the RIP sequences found in the genome/transcriptome of several important Rosaceae species, including many economically important edible fruits such as apple, pear, peac...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6274481/ https://www.ncbi.nlm.nih.gov/pubmed/27556443 http://dx.doi.org/10.3390/molecules21081105 |
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author | Shang, Chenjing Rougé, Pierre Van Damme, Els J. M. |
author_facet | Shang, Chenjing Rougé, Pierre Van Damme, Els J. M. |
author_sort | Shang, Chenjing |
collection | PubMed |
description | Ribosome-inactivating proteins (RIPs) are widespread among higher plants of different taxonomic orders. In this study, we report on the RIP sequences found in the genome/transcriptome of several important Rosaceae species, including many economically important edible fruits such as apple, pear, peach, apricot, and strawberry. All RIP domains from Rosaceae share high sequence similarity with conserved residues in the catalytic site and the carbohydrate binding sites. The genomes of Malus domestica and Pyrus communis contain both type 1 and type 2 RIP sequences, whereas for Prunus mume, Prunus persica, Pyrus bretschneideri, and Pyrus communis a complex set of type 1 RIP sequences was retrieved. Heterologous expression and purification of the type 1 as well as the type 2 RIP from apple allowed to characterize the biological activity of the proteins. Both RIPs from Malus domestica can inhibit protein synthesis. Furthermore, molecular modelling suggests that RIPs from Rosaceae possess three-dimensional structures that are highly similar to the model proteins and can bind to RIP substrates. Screening of the recombinant type 2 RIP from apple on a glycan array revealed that this type 2 RIP interacts with terminal sialic acid residues. Our data suggest that the RIPs from Rosaceae are biologically active proteins. |
format | Online Article Text |
id | pubmed-6274481 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62744812018-12-28 Ribosome Inactivating Proteins from Rosaceae Shang, Chenjing Rougé, Pierre Van Damme, Els J. M. Molecules Article Ribosome-inactivating proteins (RIPs) are widespread among higher plants of different taxonomic orders. In this study, we report on the RIP sequences found in the genome/transcriptome of several important Rosaceae species, including many economically important edible fruits such as apple, pear, peach, apricot, and strawberry. All RIP domains from Rosaceae share high sequence similarity with conserved residues in the catalytic site and the carbohydrate binding sites. The genomes of Malus domestica and Pyrus communis contain both type 1 and type 2 RIP sequences, whereas for Prunus mume, Prunus persica, Pyrus bretschneideri, and Pyrus communis a complex set of type 1 RIP sequences was retrieved. Heterologous expression and purification of the type 1 as well as the type 2 RIP from apple allowed to characterize the biological activity of the proteins. Both RIPs from Malus domestica can inhibit protein synthesis. Furthermore, molecular modelling suggests that RIPs from Rosaceae possess three-dimensional structures that are highly similar to the model proteins and can bind to RIP substrates. Screening of the recombinant type 2 RIP from apple on a glycan array revealed that this type 2 RIP interacts with terminal sialic acid residues. Our data suggest that the RIPs from Rosaceae are biologically active proteins. MDPI 2016-08-22 /pmc/articles/PMC6274481/ /pubmed/27556443 http://dx.doi.org/10.3390/molecules21081105 Text en © 2016 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Shang, Chenjing Rougé, Pierre Van Damme, Els J. M. Ribosome Inactivating Proteins from Rosaceae |
title | Ribosome Inactivating Proteins from Rosaceae |
title_full | Ribosome Inactivating Proteins from Rosaceae |
title_fullStr | Ribosome Inactivating Proteins from Rosaceae |
title_full_unstemmed | Ribosome Inactivating Proteins from Rosaceae |
title_short | Ribosome Inactivating Proteins from Rosaceae |
title_sort | ribosome inactivating proteins from rosaceae |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6274481/ https://www.ncbi.nlm.nih.gov/pubmed/27556443 http://dx.doi.org/10.3390/molecules21081105 |
work_keys_str_mv | AT shangchenjing ribosomeinactivatingproteinsfromrosaceae AT rougepierre ribosomeinactivatingproteinsfromrosaceae AT vandammeelsjm ribosomeinactivatingproteinsfromrosaceae |