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        <datestamp>2026-09-22T20:20:30Z</datestamp>
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        <oai_dc:dc xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance"  xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
          <dc:title>Enabling High-Throughput
Tissue Sectioning for Robust
Lipid Mass Spectrometry Imaging</dc:title>
          <dc:creator>Ruben Jacobs (21176991)</dc:creator>
          <dc:creator>Ritesh Chidambaram (18210761)</dc:creator>
          <dc:creator>Vincent Steinbacher (25091655)</dc:creator>
          <dc:creator>Chenwei Wei (25091658)</dc:creator>
          <dc:creator>Tim Ragan (11175963)</dc:creator>
          <dc:creator>Michiel Vandenbosch (14425444)</dc:creator>
          <dc:creator>Ron M. A. Heeren (7181636)</dc:creator>
          <dc:subject>Biophysics</dc:subject>
          <dc:subject>Biochemistry</dc:subject>
          <dc:subject>Space Science</dc:subject>
          <dc:subject>Medicine</dc:subject>
          <dc:subject>Cell Biology</dc:subject>
          <dc:subject>Genetics</dc:subject>
          <dc:subject>Physiology</dc:subject>
          <dc:subject>Biotechnology</dc:subject>
          <dc:subject>Environmental Sciences not elsewhere classified</dc:subject>
          <dc:subject>Chemical Sciences not elsewhere classified</dc:subject>
          <dc:subject>Biological Sciences not elsewhere classified</dc:subject>
          <dc:subject>Information Systems not elsewhere classified</dc:subject>
          <dc:subject>Computational  Biology</dc:subject>
          <dc:subject>spectrometry imaging toward</dc:subject>
          <dc:subject>significantly reduces sample</dc:subject>
          <dc:subject>improved biological interpretation</dc:subject>
          <dc:subject>every single section</dc:subject>
          <dc:subject>assisted laser desorption</dc:subject>
          <dc:subject>sample preparation remain</dc:subject>
          <dc:subject>resolution digital images</dc:subject>
          <dc:subject>reliable data acquisition</dc:subject>
          <dc:subject>fully automated workflow</dc:subject>
          <dc:subject>throughput tissue sectioning</dc:subject>
          <dc:subject>robust molecular information</dc:subject>
          <dc:subject>spatial resolution</dc:subject>
          <dc:subject>preparation variability</dc:subject>
          <dc:subject>acquisition time</dc:subject>
          <dc:subject>workflow demonstrating</dc:subject>
          <dc:subject>structural reference</dc:subject>
          <dc:subject>specific comparisons</dc:subject>
          <dc:subject>spatial characterization</dc:subject>
          <dc:subject>significant source</dc:subject>
          <dc:subject>serial two</dc:subject>
          <dc:subject>seamlessly integrated</dc:subject>
          <dc:subject>recent advances</dc:subject>
          <dc:subject>powerful tool</dc:subject>
          <dc:subject>pfa fixation</dc:subject>
          <dc:subject>multiplexed detection</dc:subject>
          <dc:subject>maldi workflow</dc:subject>
          <dc:subject>experimental variability</dc:subject>
          <dc:subject>enabling high</dc:subject>
          <dc:subject>downstream analyses</dc:subject>
          <dc:subject>anatomical context</dc:subject>
          <dc:subject>agarose embedding</dc:subject>
          <dc:subject>acquire high</dc:subject>
          <dc:description>Matrix-assisted laser desorption/ionization mass spectrometry
imaging
(MALDI-MSI) has been established as a powerful tool for the spatial
characterization of molecules. Recent advances have been driven by
improvements in the spatial resolution, acquisition time, and sensitivity.
Although MALDI-MSI excels in the label-free, multiplexed detection
of biomolecules, variations in sample preparation remain a significant
source of experimental variability. Here, we present a workflow demonstrating
the integration of a robust, completely automated tissue section processing
system into a MALDI workflow. Importantly, PFA fixation and agarose
embedding are demonstrated to preserve lipid compositional distributions.
Combined, it enables robust and stable lipid imaging across a completely
sectioned mouse brain. The integration of the Marinus MP system advances
mass-spectrometry imaging toward a fully automated workflow, significantly
reduces sample-preparation variability, and enables more consistent,
reliable data acquisition and improved biological interpretation.
Parallel with sectioning, serial two-photon (STP) tomography is used
to acquire high-resolution digital images of every single section,
providing a structural reference for downstream analyses. We demonstrate
how the Allen Mouse Brain Atlas can be seamlessly integrated with
these multimodal imaging data sets. This workflow enables precise
region-specific comparisons and enriches the anatomical context with
robust molecular information.</dc:description>
          <dc:date>2026-09-22T00:00:00Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.1021/acs.analchem.6c03106.s001</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/Enabling_High-Throughput_Tissue_Sectioning_for_Robust_Lipid_Mass_Spectrometry_Imaging/33968778</dc:relation>
          <dc:rights>CC BY-NC 4.0</dc:rights>
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