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Arabidopsis Plasmodesmal Proteome

The multicellular nature of plants requires that cells should communicate in order to coordinate essential functions. This is achieved in part by molecular flux through pores in the cell wall, called plasmodesmata. We describe the proteomic analysis of plasmodesmata purified from the walls of Arabid...

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Autores principales: Fernandez-Calvino, Lourdes, Faulkner, Christine, Walshaw, John, Saalbach, Gerhard, Bayer, Emmanuelle, Benitez-Alfonso, Yoselin, Maule, Andrew
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3080382/
https://www.ncbi.nlm.nih.gov/pubmed/21533090
http://dx.doi.org/10.1371/journal.pone.0018880
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author Fernandez-Calvino, Lourdes
Faulkner, Christine
Walshaw, John
Saalbach, Gerhard
Bayer, Emmanuelle
Benitez-Alfonso, Yoselin
Maule, Andrew
author_facet Fernandez-Calvino, Lourdes
Faulkner, Christine
Walshaw, John
Saalbach, Gerhard
Bayer, Emmanuelle
Benitez-Alfonso, Yoselin
Maule, Andrew
author_sort Fernandez-Calvino, Lourdes
collection PubMed
description The multicellular nature of plants requires that cells should communicate in order to coordinate essential functions. This is achieved in part by molecular flux through pores in the cell wall, called plasmodesmata. We describe the proteomic analysis of plasmodesmata purified from the walls of Arabidopsis suspension cells. Isolated plasmodesmata were seen as membrane-rich structures largely devoid of immunoreactive markers for the plasma membrane, endoplasmic reticulum and cytoplasmic components. Using nano-liquid chromatography and an Orbitrap ion-trap tandem mass spectrometer, 1341 proteins were identified. We refer to this list as the plasmodesmata- or PD-proteome. Relative to other cell wall proteomes, the PD-proteome is depleted in wall proteins and enriched for membrane proteins, but still has a significant number (35%) of putative cytoplasmic contaminants, probably reflecting the sensitivity of the proteomic detection system. To validate the PD-proteome we searched for known plasmodesmal proteins and used molecular and cell biological techniques to identify novel putative plasmodesmal proteins from a small subset of candidates. The PD-proteome contained known plasmodesmal proteins and some inferred plasmodesmal proteins, based upon sequence or functional homology with examples identified in different plant systems. Many of these had a membrane association reflecting the membranous nature of isolated structures. Exploiting this connection we analysed a sample of the abundant receptor-like class of membrane proteins and a small random selection of other membrane proteins for their ability to target plasmodesmata as fluorescently-tagged fusion proteins. From 15 candidates we identified three receptor-like kinases, a tetraspanin and a protein of unknown function as novel potential plasmodesmal proteins. Together with published work, these data suggest that the membranous elements in plasmodesmata may be rich in receptor-like functions, and they validate the content of the PD-proteome as a valuable resource for the further uncovering of the structure and function of plasmodesmata as key components in cell-to-cell communication in plants.
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spelling pubmed-30803822011-04-29 Arabidopsis Plasmodesmal Proteome Fernandez-Calvino, Lourdes Faulkner, Christine Walshaw, John Saalbach, Gerhard Bayer, Emmanuelle Benitez-Alfonso, Yoselin Maule, Andrew PLoS One Research Article The multicellular nature of plants requires that cells should communicate in order to coordinate essential functions. This is achieved in part by molecular flux through pores in the cell wall, called plasmodesmata. We describe the proteomic analysis of plasmodesmata purified from the walls of Arabidopsis suspension cells. Isolated plasmodesmata were seen as membrane-rich structures largely devoid of immunoreactive markers for the plasma membrane, endoplasmic reticulum and cytoplasmic components. Using nano-liquid chromatography and an Orbitrap ion-trap tandem mass spectrometer, 1341 proteins were identified. We refer to this list as the plasmodesmata- or PD-proteome. Relative to other cell wall proteomes, the PD-proteome is depleted in wall proteins and enriched for membrane proteins, but still has a significant number (35%) of putative cytoplasmic contaminants, probably reflecting the sensitivity of the proteomic detection system. To validate the PD-proteome we searched for known plasmodesmal proteins and used molecular and cell biological techniques to identify novel putative plasmodesmal proteins from a small subset of candidates. The PD-proteome contained known plasmodesmal proteins and some inferred plasmodesmal proteins, based upon sequence or functional homology with examples identified in different plant systems. Many of these had a membrane association reflecting the membranous nature of isolated structures. Exploiting this connection we analysed a sample of the abundant receptor-like class of membrane proteins and a small random selection of other membrane proteins for their ability to target plasmodesmata as fluorescently-tagged fusion proteins. From 15 candidates we identified three receptor-like kinases, a tetraspanin and a protein of unknown function as novel potential plasmodesmal proteins. Together with published work, these data suggest that the membranous elements in plasmodesmata may be rich in receptor-like functions, and they validate the content of the PD-proteome as a valuable resource for the further uncovering of the structure and function of plasmodesmata as key components in cell-to-cell communication in plants. Public Library of Science 2011-04-20 /pmc/articles/PMC3080382/ /pubmed/21533090 http://dx.doi.org/10.1371/journal.pone.0018880 Text en Fernandez-Calvino et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Fernandez-Calvino, Lourdes
Faulkner, Christine
Walshaw, John
Saalbach, Gerhard
Bayer, Emmanuelle
Benitez-Alfonso, Yoselin
Maule, Andrew
Arabidopsis Plasmodesmal Proteome
title Arabidopsis Plasmodesmal Proteome
title_full Arabidopsis Plasmodesmal Proteome
title_fullStr Arabidopsis Plasmodesmal Proteome
title_full_unstemmed Arabidopsis Plasmodesmal Proteome
title_short Arabidopsis Plasmodesmal Proteome
title_sort arabidopsis plasmodesmal proteome
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3080382/
https://www.ncbi.nlm.nih.gov/pubmed/21533090
http://dx.doi.org/10.1371/journal.pone.0018880
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