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Spatial Multiomics of Lipids, N-Glycans, and Tryptic Peptides on a Single FFPE Tissue Section
Author(s) -
Vanna Denti,
Giulia Capitoli,
Isabella Piga,
Francesca Clerici,
Lisa Pagani,
Lucrezia Criscuolo,
Greta Bindi,
Lucrezia Principi,
Clizia Chinello,
Giuseppe Paglia,
Fulvio Magni,
Andrew Smith
Publication year - 2022
Publication title -
journal of proteome research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.644
H-Index - 161
eISSN - 1535-3907
pISSN - 1535-3893
DOI - 10.1021/acs.jproteome.2c00601
Subject(s) - mass spectrometry imaging , computational biology , context (archaeology) , proteomics , maldi imaging , biology , pathology , glycan , molecular imaging , chemistry , mass spectrometry , microbiology and biotechnology , biochemistry , in vivo , medicine , genetics , matrix assisted laser desorption/ionization , glycoprotein , gene , paleontology , organic chemistry , chromatography , adsorption , desorption
Mass spectrometry imaging (MSI) is an emerging technology that is capable of mapping various biomolecules within their native spatial context, and performing spatial multiomics on formalin-fixed paraffin-embedded (FFPE) tissues may further increase the molecular characterization of pathological states. Here we present a novel workflow which enables the sequential MSI of lipids, N-glycans, and tryptic peptides on a single FFPE tissue section and highlight the enhanced molecular characterization that is offered by combining the multiple spatial omics data sets. In murine brain and clear cell renal cell carcinoma (ccRCC) tissue, the three molecular levels provided complementary information and characterized different histological regions. Moreover, when the spatial omics data was integrated, the different histopathological regions of the ccRCC tissue could be better discriminated with respect to the imaging data set of any single omics class. Taken together, these promising findings demonstrate the capability to more comprehensively map the molecular complexity within pathological tissue.

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