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Erratum: Spatial Multiomics of Lipids, N-Glycans, and Tryptic Peptides on a Single FFPE Tissue Section (Journal of Proteome Research (2022) 21: 11 (2798−2809) DOI: 10.1021/acs.jproteome.2c00601)

Authors :
Denti V.
Denti, V
Capitoli, G
Piga, I
Clerici, F
Pagani, L
Criscuolo, L
Bindi, G
Principi, L
Chinello, C
Paglia, G
Magni, F
Smith, A
Denti V.
Capitoli G.
Piga I.
Clerici F.
Pagani L.
Criscuolo L.
Bindi G.
Principi L.
Chinello C.
Paglia G.
Magni F.
Smith A.
Denti V.
Denti, V
Capitoli, G
Piga, I
Clerici, F
Pagani, L
Criscuolo, L
Bindi, G
Principi, L
Chinello, C
Paglia, G
Magni, F
Smith, A
Denti V.
Capitoli G.
Piga I.
Clerici F.
Pagani L.
Criscuolo L.
Bindi G.
Principi L.
Chinello C.
Paglia G.
Magni F.
Smith A.
Publication Year :
2023

Abstract

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 differ- ent 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.

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1383756526
Document Type :
Electronic Resource