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MALDI TOF Mass Spectrometry Imaging of Blood Smear: Method Development and Evaluation

The aim of this study was to develop and evaluate matrix assisted LASER desorption ionization (MALDI) time-of-flight (TOF) mass spectrometry imaging (MSI) of blood smear. Integrated light microscope and MALDI IT-TOF mass spectrometer, together with a matrix sublimation device, were used for analysis...

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Autores principales: Debeljak, Željko, Niehoff, Ann-Christin, Bandjak, Ana, Mandić, Dario, Bošnjak, Bojana, Heffer, Marija, Mrđenović, Stefan, Marković, Ivana, Zjalić, Milorad, Šerić, Vatroslav
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7827909/
https://www.ncbi.nlm.nih.gov/pubmed/33430160
http://dx.doi.org/10.3390/ijms22020585
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author Debeljak, Željko
Niehoff, Ann-Christin
Bandjak, Ana
Mandić, Dario
Bošnjak, Bojana
Heffer, Marija
Mrđenović, Stefan
Marković, Ivana
Zjalić, Milorad
Šerić, Vatroslav
author_facet Debeljak, Željko
Niehoff, Ann-Christin
Bandjak, Ana
Mandić, Dario
Bošnjak, Bojana
Heffer, Marija
Mrđenović, Stefan
Marković, Ivana
Zjalić, Milorad
Šerić, Vatroslav
author_sort Debeljak, Željko
collection PubMed
description The aim of this study was to develop and evaluate matrix assisted LASER desorption ionization (MALDI) time-of-flight (TOF) mass spectrometry imaging (MSI) of blood smear. Integrated light microscope and MALDI IT-TOF mass spectrometer, together with a matrix sublimation device, were used for analysis of blood smears coming from healthy male donors. Different blood plasma removal, matrix deposition, and instrumental settings were evaluated using the negative and positive ionization modes while agreement between the light microscopy images and the lateral distributions of cellular marker compounds served as the MSI quality indicator. Red and white blood cells chemical composition was analyzed using the differential m/z expression. Five seconds of exposure to ethanol followed by the 5 min of 9-aminoacridine or α-cyano-4-hydroxycinnamic acid deposition, together with two sets of instrumental settings, were selected for the MALDI TOF MSI experiments. Application of the thin and transparent matrix layers assured good correspondence between the LASER footprints and the preselected regions of interest. Cellular marker m/z signals coincided well with the appropriate cells. A metabolite databases search using the differentially expressed m/z produced hits which were consistent with the respective cell types. This study sets the foundations for application of blood smear MALDI TOF MSI in clinical diagnostics and research.
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spelling pubmed-78279092021-01-25 MALDI TOF Mass Spectrometry Imaging of Blood Smear: Method Development and Evaluation Debeljak, Željko Niehoff, Ann-Christin Bandjak, Ana Mandić, Dario Bošnjak, Bojana Heffer, Marija Mrđenović, Stefan Marković, Ivana Zjalić, Milorad Šerić, Vatroslav Int J Mol Sci Article The aim of this study was to develop and evaluate matrix assisted LASER desorption ionization (MALDI) time-of-flight (TOF) mass spectrometry imaging (MSI) of blood smear. Integrated light microscope and MALDI IT-TOF mass spectrometer, together with a matrix sublimation device, were used for analysis of blood smears coming from healthy male donors. Different blood plasma removal, matrix deposition, and instrumental settings were evaluated using the negative and positive ionization modes while agreement between the light microscopy images and the lateral distributions of cellular marker compounds served as the MSI quality indicator. Red and white blood cells chemical composition was analyzed using the differential m/z expression. Five seconds of exposure to ethanol followed by the 5 min of 9-aminoacridine or α-cyano-4-hydroxycinnamic acid deposition, together with two sets of instrumental settings, were selected for the MALDI TOF MSI experiments. Application of the thin and transparent matrix layers assured good correspondence between the LASER footprints and the preselected regions of interest. Cellular marker m/z signals coincided well with the appropriate cells. A metabolite databases search using the differentially expressed m/z produced hits which were consistent with the respective cell types. This study sets the foundations for application of blood smear MALDI TOF MSI in clinical diagnostics and research. MDPI 2021-01-08 /pmc/articles/PMC7827909/ /pubmed/33430160 http://dx.doi.org/10.3390/ijms22020585 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Debeljak, Željko
Niehoff, Ann-Christin
Bandjak, Ana
Mandić, Dario
Bošnjak, Bojana
Heffer, Marija
Mrđenović, Stefan
Marković, Ivana
Zjalić, Milorad
Šerić, Vatroslav
MALDI TOF Mass Spectrometry Imaging of Blood Smear: Method Development and Evaluation
title MALDI TOF Mass Spectrometry Imaging of Blood Smear: Method Development and Evaluation
title_full MALDI TOF Mass Spectrometry Imaging of Blood Smear: Method Development and Evaluation
title_fullStr MALDI TOF Mass Spectrometry Imaging of Blood Smear: Method Development and Evaluation
title_full_unstemmed MALDI TOF Mass Spectrometry Imaging of Blood Smear: Method Development and Evaluation
title_short MALDI TOF Mass Spectrometry Imaging of Blood Smear: Method Development and Evaluation
title_sort maldi tof mass spectrometry imaging of blood smear: method development and evaluation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7827909/
https://www.ncbi.nlm.nih.gov/pubmed/33430160
http://dx.doi.org/10.3390/ijms22020585
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