Publicação

An apoplastic fluid extraction method for the characterization of grapevine leaves proteome and metabolome from a single sample

Ver documento

Detalhes bibliográficos
Resumo:The analysis of complex biological systems keeps challenging researchers. The main goal of systems biology is to decipher interactions within cells, by integrating datasets from large scale analytical approaches including transcriptomics, proteomics and metabolomics andmore specialized ‘OMICS’ such as epigenomics and lipidomics. Studying different cellular compartments allows a broader understanding of cell dynamics. Plant apoplast, the cellular compartment external to the plasma membrane including the cell wall, is particularly demanding to analyze. Despite our knowledge on apoplast involvement on several processes from cell growth to stress responses, its dynamics is still poorly known due to the lack of efficient extraction processes adequate to each plant system.Analyzing woody plants such as grapevine raises even more challenges. Grapevine is among the most important fruit crops worldwide and awider characterization of its apoplast is essential for a deeper understanding of its physiology and cellular mechanisms. Here, we describe, for the first time, a vacuum-infiltrationcentrifugationmethod that allows a simultaneous extraction of grapevine apoplastic proteins and metabolites from leaves on a single sample, compatible with high-throughput mass spectrometry analyses. The extracted apoplast from two grapevine cultivars, Vitis vinifera cv ‘Trincadeira’ and ‘Regent’, was directly used for proteomics and metabolomics analysis. The proteome was analyzed by nanoLC-MS/MS and more than 700 common proteinswere identified, with highly diverse biological functions. The metabolome profile through FT-ICR-MS allowed the identification of 514 unique putative compounds revealing a broad spectrum of molecular classes
Autores principais:Figueiredo, J.
Outros Autores:Cavaco, A.R.; Guerra-Guimarães, L.; Leclerq, C.; Renaut, J.; Cunha, J.; Eiras-Dias, J.; Cordeiro, C.; Matos, A.R.; Silva, M.S.; Figueiredo, A.
Assunto:grapevine leaves proteome metabolome
Ano:2021
País:Portugal
Tipo de documento:artigo
Tipo de acesso:acesso aberto
Instituição associada:Universidade de Lisboa
Idioma:inglês
Origem:Repositório da Universidade de Lisboa
_version_ 1869346121910845440
author Figueiredo, J.
author2 Cavaco, A.R.
Guerra-Guimarães, L.
Leclerq, C.
Renaut, J.
Cunha, J.
Eiras-Dias, J.
Cordeiro, C.
Matos, A.R.
Silva, M.S.
Figueiredo, A.
author2_role author
author
author
author
author
author
author
author
author
author
author_facet Figueiredo, J.
Cavaco, A.R.
Guerra-Guimarães, L.
Leclerq, C.
Renaut, J.
Cunha, J.
Eiras-Dias, J.
Cordeiro, C.
Matos, A.R.
Silva, M.S.
Figueiredo, A.
author_role author
contributor_name_str_mv Repositório Científico de Acesso Aberto da ULisboa
country_str PT
creators_json_txt [{\"Person.name\":\"Figueiredo, J.\"},{\"Person.name\":\"Cavaco, A.R.\"},{\"Person.name\":\"Guerra-Guimarães, L.\",\"Person.identifier.orcid\":\"0000-0002-9676-1036\"},{\"Person.name\":\"Leclerq, C.\"},{\"Person.name\":\"Renaut, J.\"},{\"Person.name\":\"Cunha, J.\"},{\"Person.name\":\"Eiras-Dias, J.\"},{\"Person.name\":\"Cordeiro, C.\"},{\"Person.name\":\"Matos, A.R.\"},{\"Person.name\":\"Silva, M.S.\"},{\"Person.name\":\"Figueiredo, A.\"}]
datacite.contributors.contributor.contributorName.fl_str_mv Repositório Científico de Acesso Aberto da ULisboa
datacite.creators.creator.creatorName.fl_str_mv Figueiredo, J.
Cavaco, A.R.
Guerra-Guimarães, L.
Leclerq, C.
Renaut, J.
Cunha, J.
Eiras-Dias, J.
Cordeiro, C.
Matos, A.R.
Silva, M.S.
Figueiredo, A.
datacite.date.Accepted.fl_str_mv 2021-01-01T00:00:00Z
datacite.date.available.fl_str_mv 2022-01-28T11:12:58Z
datacite.date.embargoed.fl_str_mv 2022-01-28T11:12:58Z
datacite.rights.fl_str_mv http://purl.org/coar/access_right/c_abf2
datacite.subjects.subject.fl_str_mv grapevine leaves
proteome
metabolome
datacite.titles.title.fl_str_mv An apoplastic fluid extraction method for the characterization of grapevine leaves proteome and metabolome from a single sample
dc.contributor.none.fl_str_mv Repositório Científico de Acesso Aberto da ULisboa
dc.creator.none.fl_str_mv Figueiredo, J.
Cavaco, A.R.
Guerra-Guimarães, L.
Leclerq, C.
Renaut, J.
Cunha, J.
Eiras-Dias, J.
Cordeiro, C.
Matos, A.R.
Silva, M.S.
Figueiredo, A.
dc.date.Accepted.fl_str_mv 2021-01-01T00:00:00Z
dc.date.available.fl_str_mv 2022-01-28T11:12:58Z
dc.date.embargoed.fl_str_mv 2022-01-28T11:12:58Z
dc.format.none.fl_str_mv application/pdf
dc.identifier.none.fl_str_mv http://hdl.handle.net/10400.5/23295
dc.language.none.fl_str_mv eng
dc.publisher.none.fl_str_mv Scandinavian Plant Physiology Society
dc.rights.cclincense.fl_str_mv http://creativecommons.org/licenses/by/4.0/
dc.rights.none.fl_str_mv http://purl.org/coar/access_right/c_abf2
dc.subject.none.fl_str_mv grapevine leaves
proteome
metabolome
dc.title.fl_str_mv An apoplastic fluid extraction method for the characterization of grapevine leaves proteome and metabolome from a single sample
dc.type.none.fl_str_mv http://purl.org/coar/resource_type/c_6501
description The analysis of complex biological systems keeps challenging researchers. The main goal of systems biology is to decipher interactions within cells, by integrating datasets from large scale analytical approaches including transcriptomics, proteomics and metabolomics andmore specialized ‘OMICS’ such as epigenomics and lipidomics. Studying different cellular compartments allows a broader understanding of cell dynamics. Plant apoplast, the cellular compartment external to the plasma membrane including the cell wall, is particularly demanding to analyze. Despite our knowledge on apoplast involvement on several processes from cell growth to stress responses, its dynamics is still poorly known due to the lack of efficient extraction processes adequate to each plant system.Analyzing woody plants such as grapevine raises even more challenges. Grapevine is among the most important fruit crops worldwide and awider characterization of its apoplast is essential for a deeper understanding of its physiology and cellular mechanisms. Here, we describe, for the first time, a vacuum-infiltrationcentrifugationmethod that allows a simultaneous extraction of grapevine apoplastic proteins and metabolites from leaves on a single sample, compatible with high-throughput mass spectrometry analyses. The extracted apoplast from two grapevine cultivars, Vitis vinifera cv ‘Trincadeira’ and ‘Regent’, was directly used for proteomics and metabolomics analysis. The proteome was analyzed by nanoLC-MS/MS and more than 700 common proteinswere identified, with highly diverse biological functions. The metabolome profile through FT-ICR-MS allowed the identification of 514 unique putative compounds revealing a broad spectrum of molecular classes
dirty 0
eu_rights_str_mv openAccess
format article
fulltext.url.fl_str_mv https://repositorio.ulisboa.pt/bitstreams/70be0e96-2e64-46a6-b5d3-91a189eff8f6/download
funder_facet_str_mv FCT{{{_:::_}}}Fundação para a Ciência e a Tecnologia
FCT{{{_:::_}}}Fundação para a Ciência e a Tecnologia
FCT{{{_:::_}}}Fundação para a Ciência e a Tecnologia
funding.funder.alternateName_str_mv FCT
FCT
FCT
funding.funder.identifier_str_mv http://doi.org/10.13039/501100001871
http://doi.org/10.13039/501100001871
http://doi.org/10.13039/501100001871
funding.funder.name_str_mv Fundação para a Ciência e a Tecnologia
Fundação para a Ciência e a Tecnologia
Fundação para a Ciência e a Tecnologia
funding.identifier_str_mv UIDB/04046/2020
UIDP/04046/2020
UID/AGR/04129/2019
funding.name_str_mv 6817 - DCRRNI ID
6817 - DCRRNI ID
6817 - DCRRNI ID
funding_str_mv UIDB/04046/2020
info:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDB%2F04046%2F2020/PT
UIDP/04046/2020
info:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDP%2F04046%2F2020/PT
UID/AGR/04129/2019
info:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UID%2FAGR%2F04129%2F2019/PT
id ul_43258eb6f21eb3d2cedd26079f2bbb4d
identifier.url.fl_str_mv http://hdl.handle.net/10400.5/23295
inst_facet_str urn:organizationAcronym:ul{{{_:::_}}}Universidade de Lisboa
instacron_str ul
institution Universidade de Lisboa
instname_str Universidade de Lisboa
language eng
network_acronym_str ul
network_name_str Repositório da Universidade de Lisboa
oai_identifier_str oai:repositorio.ulisboa.pt:10400.5/23295
organization_str_mv urn:organizationAcronym:ul
person_str_mv Figueiredo, J.
Cavaco, A.R.
Guerra-Guimarães, L.
Guerra-Guimarães, L.
https://www.ciencia-id.pt/481A-FEE5-FC0A
481A-FEE5-FC0A
http://orcid.org/0000-0002-9676-1036
0000-0002-9676-1036
Leclerq, C.
Renaut, J.
Cunha, J.
Eiras-Dias, J.
Cordeiro, C.
Matos, A.R.
Silva, M.S.
Figueiredo, A.
publishDate 2021
publisher.none.fl_str_mv Scandinavian Plant Physiology Society
repo_facet_str urn:repositoryAcronym:ul{{{_:::_}}}Repositório da Universidade de Lisboa
reponame_str Repositório da Universidade de Lisboa
repository_id_str urn:repositoryAcronym:ul
service_str_mv urn:repositoryAcronym:ul
spelling engScandinavian Plant Physiology Societypt_PTThe analysis of complex biological systems keeps challenging researchers. The main goal of systems biology is to decipher interactions within cells, by integrating datasets from large scale analytical approaches including transcriptomics, proteomics and metabolomics andmore specialized ‘OMICS’ such as epigenomics and lipidomics. Studying different cellular compartments allows a broader understanding of cell dynamics. Plant apoplast, the cellular compartment external to the plasma membrane including the cell wall, is particularly demanding to analyze. Despite our knowledge on apoplast involvement on several processes from cell growth to stress responses, its dynamics is still poorly known due to the lack of efficient extraction processes adequate to each plant system.Analyzing woody plants such as grapevine raises even more challenges. Grapevine is among the most important fruit crops worldwide and awider characterization of its apoplast is essential for a deeper understanding of its physiology and cellular mechanisms. Here, we describe, for the first time, a vacuum-infiltrationcentrifugationmethod that allows a simultaneous extraction of grapevine apoplastic proteins and metabolites from leaves on a single sample, compatible with high-throughput mass spectrometry analyses. The extracted apoplast from two grapevine cultivars, Vitis vinifera cv ‘Trincadeira’ and ‘Regent’, was directly used for proteomics and metabolomics analysis. The proteome was analyzed by nanoLC-MS/MS and more than 700 common proteinswere identified, with highly diverse biological functions. The metabolome profile through FT-ICR-MS allowed the identification of 514 unique putative compounds revealing a broad spectrum of molecular classesapplication/pdfpt_PTAn apoplastic fluid extraction method for the characterization of grapevine leaves proteome and metabolome from a single sampleFigueiredo, J.Cavaco, A.R.PersonalGuerra-Guimarães, L.DSpacehttp://dspace.org/items/59fe8b32-43ad-435a-ad69-90f4ed6e5a46DSpacehttp://dspace.org/items/59fe8b32-43ad-435a-ad69-90f4ed6e5a46Guerra-GuimarãesLeonorCiência IDhttps://www.ciencia-id.pt481A-FEE5-FC0AORCIDhttp://orcid.org0000-0002-9676-1036Researcher IDhttps://www.researcherid.comHTQ-8343-2023Scopus Author IDhttps://www.scopus.com6506667079Leclerq, C.Renaut, J.Cunha, J.Eiras-Dias, J.Cordeiro, C.Matos, A.R.Silva, M.S.Figueiredo, A.HostingInstitutionOrganizationalRepositório Científico de Acesso Aberto da ULisboae-mailmailto:repositorio@ulisboa.ptrepositorio@ulisboa.ptISSNIsPartOf0031-9317DOIIsPartOf10.1111/ppl.131982022-01-28T11:12:58Z20212021-01-01T00:00:00ZHandlehttp://hdl.handle.net/10400.5/23295http://purl.org/coar/access_right/c_abf2open accessgrapevine leavesproteomemetabolome13233794 bytesFundação para a Ciência e a TecnologiaBiosystems and Integrative Sciences Instituteinfo:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDB%2F04046%2F2020/PTUIDB/04046/20206817 - DCRRNI IDCrossref Funder IDhttp://doi.org/10.13039/501100001871Fundação para a Ciência e a TecnologiaBiosystems and Integrative Sciences Instituteinfo:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDP%2F04046%2F2020/PTUIDP/04046/20206817 - DCRRNI IDCrossref Funder IDhttp://doi.org/10.13039/501100001871Fundação para a Ciência e a TecnologiaLinking Landscape, Environment, Agriculture and Foodinfo:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UID%2FAGR%2F04129%2F2019/PTUID/AGR/04129/20196817 - DCRRNI IDCrossref Funder IDhttp://doi.org/10.13039/501100001871literaturehttp://purl.org/coar/resource_type/c_6501journal article2021http://creativecommons.org/licenses/by/4.0/http://purl.org/coar/access_right/c_abf2application/pdffulltexthttps://repositorio.ulisboa.pt/bitstreams/70be0e96-2e64-46a6-b5d3-91a189eff8f6/downloadPhysiologia Plantarum
spellingShingle An apoplastic fluid extraction method for the characterization of grapevine leaves proteome and metabolome from a single sample
Figueiredo, J.
grapevine leaves
proteome
metabolome
status SINGLETON
subject.fl_str_mv grapevine leaves
proteome
metabolome
title An apoplastic fluid extraction method for the characterization of grapevine leaves proteome and metabolome from a single sample
title_full An apoplastic fluid extraction method for the characterization of grapevine leaves proteome and metabolome from a single sample
title_fullStr An apoplastic fluid extraction method for the characterization of grapevine leaves proteome and metabolome from a single sample
title_full_unstemmed An apoplastic fluid extraction method for the characterization of grapevine leaves proteome and metabolome from a single sample
title_short An apoplastic fluid extraction method for the characterization of grapevine leaves proteome and metabolome from a single sample
title_sort An apoplastic fluid extraction method for the characterization of grapevine leaves proteome and metabolome from a single sample
topic grapevine leaves
proteome
metabolome
topic_facet grapevine leaves
proteome
metabolome
url http://hdl.handle.net/10400.5/23295
visible 1

Atividades financiadas

Carregando projetos financiados...