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Updated: Jun 17, 2025

Imaging of Biological Tissues by Desorption Electrospray Ionization Mass Spectrometry
Published on: July 12, 2013
Desorption Electrospray Ionization Cyclic Ion Mobility-Mass Spectrometry Imaging for Traumatic Brain Injury Spatial
Dmitry Leontyev1, Hernando Olivos2, Bindesh Shrestha2
1School of Chemistry and Biochemistry, Georgia Institute of Technology, Atlanta, Georgia 30332, United State.
Ion mobility mass spectrometry imaging enhances lipid identification in traumatic brain injury (TBI) studies. This technique improves resolution of complex lipid species, revealing injury-induced metabolic disruptions in rat brains.
Area of Science:
- * Biochemistry and Molecular Biology
- * Neuroscience
- * Analytical Chemistry
Background:
- * Lipidomics is crucial for understanding metabolic processes and disease pathology.
- * Lipid structural diversity and isobaric/isomeric species pose identification challenges, especially in mass spectrometry imaging (MSI).
- * Ion mobility (IM) is emerging as a solution to enhance MSI capabilities.
Purpose of the Study:
- * To evaluate desorption electrospray ionization cyclic ion mobility mass spectrometry (DESI cIM MSI) for traumatic brain injury (TBI) rat brain studies.
- * To assess the impact of multiple passes in the ion mobility cell on data quality and lipid identification.
- * To identify novel lipid alterations and metabolic changes associated with TBI.
Main Methods:
- * Pilot MSI study on rat brains subjected to TBI.
- * Utilized DESI cIM MSI with one and six passes through the cyclic ion mobility cell.
- * Analyzed lipid profiles and metabolite changes, focusing on phosphoinositides, NAD, and adenine metabolites.
Main Results:
- * Increasing ion mobility passes enhanced resolving power and isobaric lipid resolution, creating more specific brain maps.
- * Drift time data revealed multiply charged phosphoinositide species, previously unreported in TBI MSI studies.
- * Observed decreased phosphoinositides in the hippocampus, reduced NAD, and altered adenine metabolites post-TBI.
Conclusions:
- * DESI cIM MSI effectively improves lipid identification and spatial mapping in TBI studies.
- * Identified novel lipid changes, including decreased phosphoinositides, suggesting altered enzymatic activity and inflammation post-TBI.
- * Confirmed significant disruption of brain energy metabolism following TBI, evidenced by NAD and adenine metabolite alterations.
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