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Spatially resolved detection of small molecules from press‐dried plant tissue using MALDI imaging
PREMISE: Matrix‐assisted laser desorption/ionization mass spectrometry imaging (MALDI‐MSI) is a chemical imaging method that can visualize spatial distributions of particular molecules. Plant tissue imaging has so far mostly used cryosectioning, which can be impractical for the preparation of large‐...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10617318/ https://www.ncbi.nlm.nih.gov/pubmed/37915436 http://dx.doi.org/10.1002/aps3.11539 |
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author | Long, Zane G. Le, Jonathan V. Katz, Benjamin B. Lopez, Belen G. Tenenbaum, Emily D. Semmling, Bonnie Schmidt, Ryan J. Grün, Felix Butts, Carter T. Martin, Rachel W. |
author_facet | Long, Zane G. Le, Jonathan V. Katz, Benjamin B. Lopez, Belen G. Tenenbaum, Emily D. Semmling, Bonnie Schmidt, Ryan J. Grün, Felix Butts, Carter T. Martin, Rachel W. |
author_sort | Long, Zane G. |
collection | PubMed |
description | PREMISE: Matrix‐assisted laser desorption/ionization mass spectrometry imaging (MALDI‐MSI) is a chemical imaging method that can visualize spatial distributions of particular molecules. Plant tissue imaging has so far mostly used cryosectioning, which can be impractical for the preparation of large‐area imaging samples, such as full flower petals. Imaging unsectioned plant tissue presents its own difficulties in extracting metabolites to the surface due to the waxy cuticle. METHODS: We address this by using established delipidation techniques combined with a solvent vapor extraction prior to applying the matrix with many low‐concentration sprays. RESULTS: Using this procedure, we imaged tissue from three different plant species (two flowers and one carnivorous plant leaf). Material factorization analysis of the resulting data reveals a wide range of plant‐specific small molecules with varying degrees of localization to specific portions of the tissue samples, while facilitating detection and removal of signal from background sources. CONCLUSIONS: This work demonstrates applicability of MALDI‐MSI to press‐dried plant samples without freezing or cryosectioning, setting the stage for spatially resolved molecule identification. Increased mass resolution and inclusion of tandem mass spectrometry are necessary next steps to allow more specific and reliable compound identification. |
format | Online Article Text |
id | pubmed-10617318 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-106173182023-11-01 Spatially resolved detection of small molecules from press‐dried plant tissue using MALDI imaging Long, Zane G. Le, Jonathan V. Katz, Benjamin B. Lopez, Belen G. Tenenbaum, Emily D. Semmling, Bonnie Schmidt, Ryan J. Grün, Felix Butts, Carter T. Martin, Rachel W. Appl Plant Sci Application Articles PREMISE: Matrix‐assisted laser desorption/ionization mass spectrometry imaging (MALDI‐MSI) is a chemical imaging method that can visualize spatial distributions of particular molecules. Plant tissue imaging has so far mostly used cryosectioning, which can be impractical for the preparation of large‐area imaging samples, such as full flower petals. Imaging unsectioned plant tissue presents its own difficulties in extracting metabolites to the surface due to the waxy cuticle. METHODS: We address this by using established delipidation techniques combined with a solvent vapor extraction prior to applying the matrix with many low‐concentration sprays. RESULTS: Using this procedure, we imaged tissue from three different plant species (two flowers and one carnivorous plant leaf). Material factorization analysis of the resulting data reveals a wide range of plant‐specific small molecules with varying degrees of localization to specific portions of the tissue samples, while facilitating detection and removal of signal from background sources. CONCLUSIONS: This work demonstrates applicability of MALDI‐MSI to press‐dried plant samples without freezing or cryosectioning, setting the stage for spatially resolved molecule identification. Increased mass resolution and inclusion of tandem mass spectrometry are necessary next steps to allow more specific and reliable compound identification. John Wiley and Sons Inc. 2023-09-11 /pmc/articles/PMC10617318/ /pubmed/37915436 http://dx.doi.org/10.1002/aps3.11539 Text en © 2023 The Authors. Applications in Plant Sciences published by Wiley Periodicals LLC on behalf of Botanical Society of America. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Application Articles Long, Zane G. Le, Jonathan V. Katz, Benjamin B. Lopez, Belen G. Tenenbaum, Emily D. Semmling, Bonnie Schmidt, Ryan J. Grün, Felix Butts, Carter T. Martin, Rachel W. Spatially resolved detection of small molecules from press‐dried plant tissue using MALDI imaging |
title | Spatially resolved detection of small molecules from press‐dried plant tissue using MALDI imaging |
title_full | Spatially resolved detection of small molecules from press‐dried plant tissue using MALDI imaging |
title_fullStr | Spatially resolved detection of small molecules from press‐dried plant tissue using MALDI imaging |
title_full_unstemmed | Spatially resolved detection of small molecules from press‐dried plant tissue using MALDI imaging |
title_short | Spatially resolved detection of small molecules from press‐dried plant tissue using MALDI imaging |
title_sort | spatially resolved detection of small molecules from press‐dried plant tissue using maldi imaging |
topic | Application Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10617318/ https://www.ncbi.nlm.nih.gov/pubmed/37915436 http://dx.doi.org/10.1002/aps3.11539 |
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