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On‐tissue chemical derivatization in mass spectrometry imaging
Mass spectrometry imaging (MSI) combines molecular and spatial information in a valuable tool for a wide range of applications. Matrix‐assisted laser desorption/ionization (MALDI) is at the forefront of MSI ionization due to its wide availability and increasing improvement in spatial resolution and...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9545000/ https://www.ncbi.nlm.nih.gov/pubmed/33433028 http://dx.doi.org/10.1002/mas.21680 |
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author | Harkin, Carla Smith, Karl W. Cruickshank, Faye L. Logan Mackay, C. Flinders, Bryn Heeren, Ron M. A. Moore, Tara Brockbank, Simon Cobice, Diego F. |
author_facet | Harkin, Carla Smith, Karl W. Cruickshank, Faye L. Logan Mackay, C. Flinders, Bryn Heeren, Ron M. A. Moore, Tara Brockbank, Simon Cobice, Diego F. |
author_sort | Harkin, Carla |
collection | PubMed |
description | Mass spectrometry imaging (MSI) combines molecular and spatial information in a valuable tool for a wide range of applications. Matrix‐assisted laser desorption/ionization (MALDI) is at the forefront of MSI ionization due to its wide availability and increasing improvement in spatial resolution and analysis speed. However, ionization suppression, low concentrations, and endogenous and methodological interferences cause visualization problems for certain molecules. Chemical derivatization (CD) has proven a viable solution to these issues when applied in mass spectrometry platforms. Chemical tagging of target analytes with larger, precharged moieties aids ionization efficiency and removes analytes from areas of potential isobaric interferences. Here, we address the application of CD on tissue samples for MSI analysis, termed on‐tissue chemical derivatization (OTCD). MALDI MSI will remain the focus platform due to its popularity, however, alternative ionization techniques such as liquid extraction surface analysis and desorption electrospray ionization will also be recognized. OTCD reagent selection, application, and optimization methods will be discussed in detail. MSI with OTCD is a powerful tool to study the spatial distribution of poorly ionizable molecules within tissues. Most importantly, the use of OTCD−MSI facilitates the analysis of previously inaccessible biologically relevant molecules through the adaptation of existing CD methods. Though further experimental optimization steps are necessary, the benefits of this technique are extensive. |
format | Online Article Text |
id | pubmed-9545000 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95450002022-10-14 On‐tissue chemical derivatization in mass spectrometry imaging Harkin, Carla Smith, Karl W. Cruickshank, Faye L. Logan Mackay, C. Flinders, Bryn Heeren, Ron M. A. Moore, Tara Brockbank, Simon Cobice, Diego F. Mass Spectrom Rev Review Articles Mass spectrometry imaging (MSI) combines molecular and spatial information in a valuable tool for a wide range of applications. Matrix‐assisted laser desorption/ionization (MALDI) is at the forefront of MSI ionization due to its wide availability and increasing improvement in spatial resolution and analysis speed. However, ionization suppression, low concentrations, and endogenous and methodological interferences cause visualization problems for certain molecules. Chemical derivatization (CD) has proven a viable solution to these issues when applied in mass spectrometry platforms. Chemical tagging of target analytes with larger, precharged moieties aids ionization efficiency and removes analytes from areas of potential isobaric interferences. Here, we address the application of CD on tissue samples for MSI analysis, termed on‐tissue chemical derivatization (OTCD). MALDI MSI will remain the focus platform due to its popularity, however, alternative ionization techniques such as liquid extraction surface analysis and desorption electrospray ionization will also be recognized. OTCD reagent selection, application, and optimization methods will be discussed in detail. MSI with OTCD is a powerful tool to study the spatial distribution of poorly ionizable molecules within tissues. Most importantly, the use of OTCD−MSI facilitates the analysis of previously inaccessible biologically relevant molecules through the adaptation of existing CD methods. Though further experimental optimization steps are necessary, the benefits of this technique are extensive. John Wiley and Sons Inc. 2021-01-12 2022 /pmc/articles/PMC9545000/ /pubmed/33433028 http://dx.doi.org/10.1002/mas.21680 Text en © 2021 The Authors. Mass Spectrometry Reviews published by John Wiley & Sons Ltd. 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 | Review Articles Harkin, Carla Smith, Karl W. Cruickshank, Faye L. Logan Mackay, C. Flinders, Bryn Heeren, Ron M. A. Moore, Tara Brockbank, Simon Cobice, Diego F. On‐tissue chemical derivatization in mass spectrometry imaging |
title | On‐tissue chemical derivatization in mass spectrometry imaging |
title_full | On‐tissue chemical derivatization in mass spectrometry imaging |
title_fullStr | On‐tissue chemical derivatization in mass spectrometry imaging |
title_full_unstemmed | On‐tissue chemical derivatization in mass spectrometry imaging |
title_short | On‐tissue chemical derivatization in mass spectrometry imaging |
title_sort | on‐tissue chemical derivatization in mass spectrometry imaging |
topic | Review Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9545000/ https://www.ncbi.nlm.nih.gov/pubmed/33433028 http://dx.doi.org/10.1002/mas.21680 |
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