Literature DB >> 28012871

Quantification of low molecular weight compounds by MALDI imaging mass spectrometry - A tutorial review.

Ignacy Rzagalinski1, Dietrich A Volmer2.   

Abstract

Matrix-assisted laser desorption/ionization (MALDI)-mass spectrometry imaging (MSI) permits label-free in situ analysis of chemical compounds directly from the surface of two-dimensional biological tissue slices. It links qualitative molecular information of compounds to their spatial coordinates and distribution within the investigated tissue. MALDI-MSI can also provide the quantitative amounts of target compounds in the tissue, if proper calibration techniques are performed. Obviously, as the target molecules are embedded within the biological tissue environment and analysis must be performed at their precise locations, there is no possibility for extensive sample clean-up routines or chromatographic separations as usually performed with homogenized biological materials; ion suppression phenomena therefore become a critical side effect of MALDI-MSI. Absolute quantification by MALDI-MSI should provide an accurate value of the concentration/amount of the compound of interest in relatively small, well-defined region of interest of the examined tissue, ideally in a single pixel. This goal is extremely challenging and will not only depend on the technical possibilities and limitations of the MSI instrument hardware, but equally on the chosen calibration/standardization strategy. These strategies are the main focus of this article and are discussed and contrasted in detail in this tutorial review. This article is part of a Special Issue entitled: MALDI Imaging, edited by Dr. Corinna Henkel and Prof. Peter Hoffmann.
Copyright © 2016 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Calibration; Low molecular weight compounds; MALDI-MSI; Matrix-assisted laser desorption/ionization, imaging mass Spectrometry; Normalization; Quantification

Mesh:

Year:  2016        PMID: 28012871     DOI: 10.1016/j.bbapap.2016.12.011

Source DB:  PubMed          Journal:  Biochim Biophys Acta Proteins Proteom        ISSN: 1570-9639            Impact factor:   3.036


  22 in total

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