Spatial segmentation of MALDI FT-ICR MSI data: a powerful tool to explore the head and neck tumor in situ lipidome
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
- MeSH
- Fourierova analýza MeSH
- lidé MeSH
- lipidy analýza chemie MeSH
- molekulární zobrazování metody MeSH
- nádory hlavy a krku chemie MeSH
- počítačové zpracování obrazu MeSH
- spektrometrie hmotnostní - ionizace laserem za účasti matrice metody MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- lipidy MeSH
Matrix-assisted laser desorption/ionization mass spectrometric imaging (MALDI MSI) is a well-established analytical technique for determining spatial localization of lipids in biological samples. The use of Fourier-transform ion cyclotron resonance (FT-ICR) mass spectrometers for the molecular imaging of endogenous compounds is gaining popularity, since the high mass accuracy and high mass resolving power enables accurate determination of exact masses and, consequently, a more confident identification of these molecules. The high mass resolution FT-ICR imaging datasets are typically large in size. In order to analyze them in an appropriate timeframe, the following approach has been employed: the FT-ICR imaging datasets were spatially segmented by clustering all spectra by their similarity. The resulted spatial segmentation maps were compared with the histologic annotation. This approach facilitates interpretation of the full datasets by providing spatial regions of interest. The application of this approach, which has originally been developed for MALDI-TOF MSI datasets, to the lipidomic analysis of head and neck tumor tissue revealed new insights into the metabolic organization of the carcinoma tissue.
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Anal Chem. 2010 Jun 1;82(11):4648-51 PubMed
Analyst. 2013 Mar 7;138(5):1289-315 PubMed
Anal Chem. 1997 Dec 1;69(23):4751-60 PubMed
Crit Rev Biochem Mol Biol. 2013 Jan-Feb;48(1):20-38 PubMed
J Lipid Res. 2010 Aug;51(8):2295-302 PubMed
J Cancer Res Clin Oncol. 2013 Jan;139(1):85-95 PubMed
J Histochem Cytochem. 2010 Oct;58(10):929-37 PubMed
Mol Oncol. 2014 Feb;8(1):39-49 PubMed
Anal Bioanal Chem. 2014 Feb;406(5):1307-16 PubMed
J Lipid Res. 2013 Feb;54(2):333-44 PubMed
Proteomics. 2008 Sep;8(18):3801-8 PubMed
J Proteome Res. 2010 Dec 3;9(12):6535-46 PubMed
J Biol Chem. 1957 May;226(1):497-509 PubMed
Histochem Cell Biol. 2013 Jun;139(6):759-83 PubMed
Biochemistry. 2013 Jun 4;52(22):3818-28 PubMed
Anal Chem. 2012 Jul 17;84(14):6079-87 PubMed
Proteomics. 2014 Apr;14(7-8):913-23 PubMed
Plant Cell. 2012 Feb;24(2):622-36 PubMed