4.8 Article

Multimodal Mass Spectrometry Imaging of N-Glycans and Proteins from the Same Tissue Section

Journal

ANALYTICAL CHEMISTRY
Volume 88, Issue 15, Pages 7745-7753

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.analchem.6b01739

Keywords

-

Funding

  1. ZonMW Zenith project Imaging Mass Spectrometry-Based Molecular Histology: Differentiation and Characterization of Clinically Challenging Soft Tissue Sarcomas [93512002]
  2. European Union Seventh Framework Programmes HighGlycan project [278535]
  3. National Institutes of Health/National Cancer Institute [R21CA186799]
  4. state of South Carolina SmartState Endowed Research program
  5. National Cancer Institute (NCI) [R01 CA120206, U01 CA168856]
  6. Hepatitis B Foundation

Ask authors/readers for more resources

On-tissue digestion matrix-assisted laser desorption/ionization mass spectrometry imaging (MALDI-MSI) can be used to record spatially correlated molecular information from formalin-fixed, paraffin-embedded (FFPE) tissue sections. In this work, we present the in situ multimodal analysis of N-linked glycans and proteins from the same FFPE tissue section. The robustness and applicability of the method are demonstrated for several tumors, including epithelial and mesenchymal tumor types. Major analytical aspects, such as lateral diffusion of the analyte molecules and differences in measurement sensitivity due to the additional sample preparation methods, have been investigated for both N-glycans and proteolytic peptides. By combining the MSI approach with extract analysis, we were also able to assess which mass spectral peaks generated by MALDI-MSI could be assigned to unique N-glycan and peptide identities.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available