Title of article
Mass spectrometry imaging is moving toward drug protein co-localization
Author/Authors
Rima Ait-Belkacem، نويسنده , , Lyna Sellami، نويسنده , , Claude Villard، نويسنده , , Edwin DePauw، نويسنده , , David Calligaris، نويسنده , , Daniel Lafitte، نويسنده ,
Issue Information
ماهنامه با شماره پیاپی سال 2012
Pages
9
From page
466
To page
474
Abstract
Mass spectrometry (MS)-based technology provides label-free localization of molecules in tissue samples. Drugs, proteins, lipids and metabolites can easily be monitored in their environment. Resolution can be achieved down to the cellular level (10–20 μm) for conventional matrix-assisted laser desorption/ionization (MALDI) imaging, or even to the subcellular level for more complex technologies such as secondary ionization mass spectrometry (SIMS) imaging. One question remains: are we going to be able to investigate functional relationships between drugs and proteins and compare with localized phenomena? This review describes the various spatial levels of investigation offered by mass spectrometry imaging (MSI), and the advantages and disadvantages compared with other labeling technologies.
Journal title
Trends in Biotechnology
Serial Year
2012
Journal title
Trends in Biotechnology
Record number
1233833
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