4.6 Article

Device-Controlled Microcondensation for Spatially Confined On-Tissue Digests in MALDI Imaging of N-Glycans

Journal

PHARMACEUTICALS
Volume 15, Issue 11, Pages -

Publisher

MDPI
DOI: 10.3390/ph15111356

Keywords

MALDI MSI; N-glycans; enzymatic digestion; micro-condensation; standardization

Funding

  1. German Federal Ministry of Economics and Energy (BMWi) [ZF4560202BA8]
  2. German Federal Ministry of Economics and Energy (BMWi from the ZIM Kooperationsprojekte program)
  3. Deutsche Forschungsgemeinschaft (DFG) [SFB 1389, 404521405]
  4. Hector Foundation II

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On-tissue enzymatic digestion is crucial for analyzing tissue proteins and their N-glycan conjugates. However, the current sample preparation method is mainly carried out by specialized laboratories using home-built arrangements, which lack standardization. To address this, a digestion device that controls humidity and monitors the digestion process was designed.
On-tissue enzymatic digestion is a prerequisite for MALDI mass spectrometry imaging (MSI) and spatialomic analysis of tissue proteins and their N-glycan conjugates. Despite the more widely accepted importance of N-glycans as diagnostic and prognostic biomarkers of many diseases and their potential as pharmacodynamic markers, the crucial sample preparation step, namely on-tissue digestion with enzymes like PNGaseF, is currently mainly carried out by specialized laboratories using home-built incubation arrangements, e.g., petri dishes placed in an incubator. Standardized spatially confined enzyme digests, however, require precise control and possible regulation of humidity and temperature, as high humidity increases the risk of analyte dislocation and low humidity compromises enzyme function. Here, a digestion device that controls humidity by cyclic ventilation and heating of the slide holder and the chamber lid was designed to enable controlled micro-condensation on the slide and to stabilize and monitor the digestion process. The device presented here may help with standardization in MSI. Using sagittal mouse brain sections and xenografted human U87 glioblastoma cells in CD1 nu/nu mouse brain, a device-controlled workflow for MALDI MSI of N-glycans was developed.

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