4.7 Article

High-resolution imaging and identification of biomolecules using Nano-DESI coupled to ion mobility spectrometry

Journal

ANALYTICA CHIMICA ACTA
Volume 1186, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.aca.2021.339085

Keywords

Ion mobility spectrometry; Mass spectrometry imaging; Collision cross section; Lipidomics; Isomeric separation

Funding

  1. National Science Foundation [NSF-1808136, NSF-2108729]
  2. National Institute of Health [R01HD068524-4, R01HD103475-25]
  3. National Science Foundation Graduate Research Fellowship [DGE-1333468]

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The study introduces a novel experimental platform that combines nano-DESI and IM spectrometry for high spatial resolution imaging of molecules in mouse uterine tissues, providing unique molecular descriptors and revealing variations in isomeric composition through isomer-specific imaging.
Simultaneous spatial localization and structural characterization of molecules in complex biological samples currently represents an analytical challenge for mass spectrometry imaging (MSI) techniques. In this study, we describe a novel experimental platform, which substantially expands the capabilities and enhances the depth of chemical information obtained in high spatial resolution MSI experiments performed using nanospray desorption electrospray ionization (nano-DESI). Specifically, we designed and constructed a portable nano-DESI MSI platform and coupled it with a drift tube ion mobility (IM) spectrometer-mass spectrometer. We demonstrate imaging of drift time-separated ions with a high spatial resolution of better than similar to 25 mu m using uterine tissues on day 4 of pregnancy in mice. Collision cross-section measurements provide unique molecular descriptors of molecules observed in nano-DESI-IM-MSI necessary for their unambiguous identification by comparison with databases. Meanwhile, isomer-specific imaging reveals variations in the isomeric composition across the tissue. Furthermore, IM separation efficiently eliminates isobaric and isomeric interferences originating from solvent peaks, overlapping isotopic peaks of endogenous molecules extracted from the tissue, and products of in-source fragmentation, which is critical to obtaining accurate concentration gradients in the sample using MSI. The structural information provided by the IM separation substantially expands the molecular specificity of high-resolution MSI necessary for unraveling the complexity of biological systems. (C) 2021 Elsevier B.V. All rights reserved.

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