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  • Lipidomics for clinical diagnosis: Dye-Assisted Laser Desorption/Ionization (DALDI) method for lipids detection in MALDI mass spectrometry imaging.

Lipidomics for clinical diagnosis: Dye-Assisted Laser Desorption/Ionization (DALDI) method for lipids detection in MALDI mass spectrometry imaging.

Omics : a journal of integrative biology (2014-06-07)
Karim Arafah, Rémi Longuespée, Annie Desmons, Olivier Kerdraon, Isabelle Fournier, Michel Salzet
ABSTRACT

Lipid-based biomarkers for research and diagnosis are rapidly emerging to unpack the basis of person-to-person and population variations in disease susceptibility, drug and nutritional responses, to name but a few. Hence, with the advent of MALDI Mass Spectrometry Imaging, lipids have begun to be investigated intensively. However, lipids are highly mobile during tissue preparation, and are soluble in the solvent used for matrix preparation or in the fixing fluid such as formalin, resulting in substantial delocalization. In the present article, we investigated as another alternative, the possibility of using specific dyes that can absorb UV wavelengths, in order to desorb the lipids specifically from tissue sections, and are known to immobilize them in tissues. Indeed, after lipid insolubilization with chromate solution or chemical fixation with osmium tetroxide, heterocyclic-based dyes can be directly used without matrix. Taking into account the fact that some dyes have this matrix-free capability, we identified particular dyes dedicated to histological staining of lipids that could be used with MALDI mass spectrometry imaging. We stained tissue sections with either Sudan Black B, Nile Blue A, or Oil Red O. An important advantage of this assay relies on its compatibility with usual practices of histopathological investigation of lipids. As a new method, DALDI stands for Dye-Assisted Laser Desorption Ionization and allows for future clinical and histopathological applications using routine histological protocols. Additionally, this novel methodology was validated in human ovarian cancer biopsies to demonstrate its use as a suitable procedure, for histological diagnosis in lipidomics field.

MATERIALS
Product Number
Brand
Product Description

Supelco
Ethanol solution, certified reference material, 2000 μg/mL in methanol
Sigma-Aldrich
Osmium tetroxide, Sealed ampule.
Supelco
Dehydrated Alcohol, Pharmaceutical Secondary Standard; Certified Reference Material
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Os EnCat® 40, extent of labeling: 0.3 mmol/g Os loading
USP
Dehydrated Alcohol, United States Pharmacopeia (USP) Reference Standard
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Osmium tetroxide, ACS reagent, ≥98.0%
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Osmium tetroxide, ReagentPlus®, 99.8%
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Ethanol, tested according to Ph. Eur.
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Ethanol, for residue analysis
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Osmium tetroxide solution, suitable for electron microscopy, 2% in H2O
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Ethanol, purum, secunda spirit, denaturated with 2% 2-butanone, S15, ~96% (based on denaturant-free substance)
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Ethyl alcohol, Pure, 190 proof, ACS spectrophotometric grade, 95.0%
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Osmium tetroxide solution, suitable for electron microscopy, 4% in H2O
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Ethanol, BioUltra, for molecular biology, ≥99.8%, (absolute alcohol, without additive, A15 o1)
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Ethanol, purum, fine spirit, denaturated with 4.8% methanol, F25 METHYL1, ~96% (based on denaturant-free substance)
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Ethanol, purum, absolute ethanol, denaturated with 4.8% isopropanol, A15 IPA1, ≥99.8% (based on denaturant-free substance)
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Ethanol, purum, fine spirit, denaturated with 2% 2-butanone, F25 MEK1, ~96% (based on denaturant-free substance)
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Ethanol, purum, absolute ethanol, denaturated with 2% 2-butanone, A15 MEK1, ≥99.8% (based on denaturant-free substance)
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Ethyl alcohol, Pure, 200 proof, meets USP testing specifications
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Ethyl alcohol, Pure, 200 proof, ACS reagent, ≥99.5%
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Osmium tetroxide solution, 4 wt. % in H2O
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Ethyl alcohol, Pure, 200 proof, for molecular biology
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Ethyl alcohol, Pure, 190 proof, for molecular biology
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Osmium tetroxide solution, 2.5 wt. % in tert-butanol