4.5 Review

On-tissue chemical derivatization in mass spectrometry imaging

Journal

MASS SPECTROMETRY REVIEWS
Volume 41, Issue 5, Pages 662-694

Publisher

WILEY
DOI: 10.1002/mas.21680

Keywords

chemical derivatization; mass spectrometry imaging; matrix-assisted laser desorption ionization

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Mass spectrometry imaging (MSI) combines molecular and spatial information, making it a valuable tool in various applications. Chemical derivatization (CD) has proven to be an effective solution for ionization issues. On-tissue chemical derivatization (OTCD) is a powerful tool for studying the spatial distribution of poorly ionizable molecules within tissues.
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.

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