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High-mass-resolution MALDI mass spectrometry imaging of metabolites from formalin-fixed paraffin-embedded tissue.
Nat. Protoc. 11, 1428-1443 (2016)
Formalin-fixed and paraffin-embedded (FFPE) tissue specimens are the gold standard for histological examination, and they provide valuable molecular information in tissue-based research. Metabolite assessment from archived tissue samples has not been extensively conducted because of a lack of appropriate protocols and concerns about changes in metabolite content or chemical state due to tissue processing. We present a protocol for the in situ analysis of metabolite content from FFPE samples using a high-mass-resolution matrix-assisted laser desorption/ionization fourier-transform ion cyclotron resonance mass spectrometry imaging (MALDI-FT-ICR-MSI) platform. The method involves FFPE tissue sections that undergo deparaffinization and matrix coating by 9-aminoacridine before MALDI-MSI. Using this platform, we previously detected ∼1,500 m/z species in the mass range m/z 50-1,000 in FFPE samples; the overlap compared with fresh frozen samples is 72% of m/z species, indicating that metabolites are largely conserved in FFPE tissue samples. This protocol can be reproducibly performed on FFPE tissues, including small samples such as tissue microarrays and biopsies. The procedure can be completed in a day, depending on the size of the sample measured and raster size used. Advantages of this approach include easy sample handling, reproducibility, high throughput and the ability to demonstrate molecular spatial distributions in situ. The data acquired with this protocol can be used in research and clinical practice.
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Publication type
Article: Journal article
Document type
Scientific Article
Keywords
Assisted-laser-desorption/ionization; Multivariate Data-analysis; Breast-cancer Tissues; Sample Preparation; Nmr-spectroscopy; Ms Analysis; Matrix; Metabolomics; Specimens; Cells
Language
Publication Year
2016
HGF-reported in Year
2016
ISSN (print) / ISBN
1754-2189
e-ISSN
1750-2799
Journal
Nature Protocols
Quellenangaben
Volume: 11,
Issue: 8,
Pages: 1428-1443
Publisher
Nature Publishing Group
Publishing Place
London
Reviewing status
Peer reviewed
Institute(s)
Research Unit Analytical Pathology (AAP)
Institute of Pathology (PATH)
Translational Metabolic Oncology (IDC-TMO)
Institute of Pathology (PATH)
Translational Metabolic Oncology (IDC-TMO)
POF-Topic(s)
30205 - Bioengineering and Digital Health
30504 - Mechanisms of Genetic and Environmental Influences on Health and Disease
30203 - Molecular Targets and Therapies
30504 - Mechanisms of Genetic and Environmental Influences on Health and Disease
30203 - Molecular Targets and Therapies
Research field(s)
Enabling and Novel Technologies
Radiation Sciences
Radiation Sciences
PSP Element(s)
G-500390-001
G-500300-001
G-501000-001
G-500300-001
G-501000-001
WOS ID
WOS:000379814300009
Scopus ID
84979912993
PubMed ID
27414759
Erfassungsdatum
2016-07-26