Cargando…

Broad‐range metalloprotease profiling in plants uncovers immunity provided by defence‐related metalloenzyme

Plants encode > 100 metalloproteases representing > 19 different protein families. Tools to study this large and diverse class of proteases have not yet been introduced into plant research. We describe the use of hydroxamate‐based photoaffinity probes to explore plant proteomes for metalloprot...

Descripción completa

Detalles Bibliográficos
Autores principales: Morimoto, Kyoko, Krahn, Daniel, Kaschani, Farnusch, Hopkinson‐Woolley, Digby, Gee, Anna, Buscaill, Pierre, Mohammed, Shabaz, Sieber, Stephan A., Cravatt, Benjamin F., Schofield, Christopher J., van der Hoorn, Renier A. L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9322406/
https://www.ncbi.nlm.nih.gov/pubmed/35510806
http://dx.doi.org/10.1111/nph.18200
_version_ 1784756295708966912
author Morimoto, Kyoko
Krahn, Daniel
Kaschani, Farnusch
Hopkinson‐Woolley, Digby
Gee, Anna
Buscaill, Pierre
Mohammed, Shabaz
Sieber, Stephan A.
Cravatt, Benjamin F.
Schofield, Christopher J.
van der Hoorn, Renier A. L.
author_facet Morimoto, Kyoko
Krahn, Daniel
Kaschani, Farnusch
Hopkinson‐Woolley, Digby
Gee, Anna
Buscaill, Pierre
Mohammed, Shabaz
Sieber, Stephan A.
Cravatt, Benjamin F.
Schofield, Christopher J.
van der Hoorn, Renier A. L.
author_sort Morimoto, Kyoko
collection PubMed
description Plants encode > 100 metalloproteases representing > 19 different protein families. Tools to study this large and diverse class of proteases have not yet been introduced into plant research. We describe the use of hydroxamate‐based photoaffinity probes to explore plant proteomes for metalloproteases. We detected labelling of 23 metalloproteases in leaf extracts of the model plant Arabidopsis thaliana that belong to nine different metalloprotease families and localize to different subcellular compartments. The probes identified several chloroplastic FtsH proteases, vacuolar aspartyl aminopeptidase DAP1, peroxisomal metalloprotease PMX16, extracellular matrix metalloproteases and many cytosolic metalloproteases. We also identified nonproteolytic metallohydrolases involved in the release of auxin and in the urea cycle. Studies on tobacco plants (Nicotiana benthamiana) infected with the bacterial plant pathogen Pseudomonas syringae uncovered the induced labelling of PRp27, a secreted protein with implicated metalloprotease activity. PRp27 overexpression increases resistance, and PRp27 mutants lacking metal binding site are no longer labelled, but still show increased immunity. Collectively, these studies reveal the power of broad‐range metalloprotease profiling in plants using hydroxamate‐based probes.
format Online
Article
Text
id pubmed-9322406
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-93224062022-07-30 Broad‐range metalloprotease profiling in plants uncovers immunity provided by defence‐related metalloenzyme Morimoto, Kyoko Krahn, Daniel Kaschani, Farnusch Hopkinson‐Woolley, Digby Gee, Anna Buscaill, Pierre Mohammed, Shabaz Sieber, Stephan A. Cravatt, Benjamin F. Schofield, Christopher J. van der Hoorn, Renier A. L. New Phytol Research Plants encode > 100 metalloproteases representing > 19 different protein families. Tools to study this large and diverse class of proteases have not yet been introduced into plant research. We describe the use of hydroxamate‐based photoaffinity probes to explore plant proteomes for metalloproteases. We detected labelling of 23 metalloproteases in leaf extracts of the model plant Arabidopsis thaliana that belong to nine different metalloprotease families and localize to different subcellular compartments. The probes identified several chloroplastic FtsH proteases, vacuolar aspartyl aminopeptidase DAP1, peroxisomal metalloprotease PMX16, extracellular matrix metalloproteases and many cytosolic metalloproteases. We also identified nonproteolytic metallohydrolases involved in the release of auxin and in the urea cycle. Studies on tobacco plants (Nicotiana benthamiana) infected with the bacterial plant pathogen Pseudomonas syringae uncovered the induced labelling of PRp27, a secreted protein with implicated metalloprotease activity. PRp27 overexpression increases resistance, and PRp27 mutants lacking metal binding site are no longer labelled, but still show increased immunity. Collectively, these studies reveal the power of broad‐range metalloprotease profiling in plants using hydroxamate‐based probes. John Wiley and Sons Inc. 2022-05-26 2022-08 /pmc/articles/PMC9322406/ /pubmed/35510806 http://dx.doi.org/10.1111/nph.18200 Text en © 2022 The Authors. New Phytologist © 2022 New Phytologist Foundation https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Morimoto, Kyoko
Krahn, Daniel
Kaschani, Farnusch
Hopkinson‐Woolley, Digby
Gee, Anna
Buscaill, Pierre
Mohammed, Shabaz
Sieber, Stephan A.
Cravatt, Benjamin F.
Schofield, Christopher J.
van der Hoorn, Renier A. L.
Broad‐range metalloprotease profiling in plants uncovers immunity provided by defence‐related metalloenzyme
title Broad‐range metalloprotease profiling in plants uncovers immunity provided by defence‐related metalloenzyme
title_full Broad‐range metalloprotease profiling in plants uncovers immunity provided by defence‐related metalloenzyme
title_fullStr Broad‐range metalloprotease profiling in plants uncovers immunity provided by defence‐related metalloenzyme
title_full_unstemmed Broad‐range metalloprotease profiling in plants uncovers immunity provided by defence‐related metalloenzyme
title_short Broad‐range metalloprotease profiling in plants uncovers immunity provided by defence‐related metalloenzyme
title_sort broad‐range metalloprotease profiling in plants uncovers immunity provided by defence‐related metalloenzyme
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9322406/
https://www.ncbi.nlm.nih.gov/pubmed/35510806
http://dx.doi.org/10.1111/nph.18200
work_keys_str_mv AT morimotokyoko broadrangemetalloproteaseprofilinginplantsuncoversimmunityprovidedbydefencerelatedmetalloenzyme
AT krahndaniel broadrangemetalloproteaseprofilinginplantsuncoversimmunityprovidedbydefencerelatedmetalloenzyme
AT kaschanifarnusch broadrangemetalloproteaseprofilinginplantsuncoversimmunityprovidedbydefencerelatedmetalloenzyme
AT hopkinsonwoolleydigby broadrangemetalloproteaseprofilinginplantsuncoversimmunityprovidedbydefencerelatedmetalloenzyme
AT geeanna broadrangemetalloproteaseprofilinginplantsuncoversimmunityprovidedbydefencerelatedmetalloenzyme
AT buscaillpierre broadrangemetalloproteaseprofilinginplantsuncoversimmunityprovidedbydefencerelatedmetalloenzyme
AT mohammedshabaz broadrangemetalloproteaseprofilinginplantsuncoversimmunityprovidedbydefencerelatedmetalloenzyme
AT sieberstephana broadrangemetalloproteaseprofilinginplantsuncoversimmunityprovidedbydefencerelatedmetalloenzyme
AT cravattbenjaminf broadrangemetalloproteaseprofilinginplantsuncoversimmunityprovidedbydefencerelatedmetalloenzyme
AT schofieldchristopherj broadrangemetalloproteaseprofilinginplantsuncoversimmunityprovidedbydefencerelatedmetalloenzyme
AT vanderhoornrenieral broadrangemetalloproteaseprofilinginplantsuncoversimmunityprovidedbydefencerelatedmetalloenzyme