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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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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 |
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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 |
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