Abstract Mass spectrometry imaging (MSI) of volatile metabolites is challenging, especially in matrix‐assisted laser desorption/ionization (MALDI). Most MALDI ion sources operate in vacuum, which leads to the vaporization of volatile metabolites during analysis. In addition, tissue samples are often dried during sample preparation, leading to the loss of volatile metabolites even for other MSI techniques. On‐tissue chemical derivatization can dramatically reduce the volatility of analytes. Herein, a derivatization method is proposed utilizing N,N,N‐trimethyl‐2‐(piperazin‐1‐yl)ethan‐1‐aminium iodide to chemically modify short‐chain fatty acids in chicken cecum, ileum, and jejunum tissue sections before sample preparation for MSI visualization.
more »
« less
This content will become publicly available on April 8, 2026
Universal Photosensitizer for Isomer-Selective Lipid Imaging with High Molecular Coverage
Spatial lipidomics is a powerful technique for understanding the complexity of the lipidome in biological systems through mass spectrometry imaging (MSI). Recent advancements have enabled isomer-selected MSI (iMSI) of lipids in biological samples using both online and off-line derivatization strategies. Despite these impressive developments, most iMSI techniques are limited to either positive or negative ion mode analysis, restricting the molecular coverage achievable in a single experiment. Additionally, derivatization efficiency often varies across lipid classes, presenting challenges for comprehensive lipid analysis. In this study, we introduce tetrakis(4-carboxyphenyl)porphyrin (TCPP) as a universal photosensitizer that facilitates online lipid derivatization in both positive and negative ionization modes via singlet oxygen (1O2) reaction. This method enables the identification and localization of both acyl chain compositions and lipid carbon-carbon (C=C) isomers in liquid extraction-based ambient ionization techniques. We have also employed sodium fluoride (NaF) as a solvent dopant to enhance the analysis of low-abundance and poorly ionizable biomolecules. By integrating these online derivatization and signal enhancement strategies with nanospray desorption electrospray ionization (nano-DESI), we achieved dual polarity iMSI within the same sample. We demonstrate imaging of low-abundance isomeric lipids, which were otherwise below the noise level. Notably, TCPP significantly enhances the efficiency of the online derivatization of unsaturated fatty acids, for which other photosensitizers are inefficient. This novel approach allows for the imaging of isomeric fatty acids and phospholipids from multiple classes in the same experiment, revealing their distinct spatial localization within biological tissues.
more »
« less
- Award ID(s):
- 2108729
- PAR ID:
- 10587739
- Publisher / Repository:
- ACS
- Date Published:
- Journal Name:
- Analytical Chemistry
- Volume:
- 97
- Issue:
- 13
- ISSN:
- 0003-2700
- Page Range / eLocation ID:
- 7071 to 7078
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
More Like this
-
-
Lee, YJ (Ed.)The ability to study and visualize metabolites on a cellular and sub-cellular level is important for gaining insights into biological pathways and metabolism of multicellular organisms. Matrix-assisted laser desorption/ionization (MALDI) mass spectrometry imaging (MSI) is a powerful analytical tool for metabolomics experiments due to its high sensitivity and small sampling size. The spatial resolution in MALDI-MSI is mainly limited by the number of molecules available in a small sampling size. When the sampling size is low enough to achieve cellular or subcellular spatial resolution, signal intensity is sacrificed making poorly ionized metabolites difficult to detect. To overcome this limitation, on-tissue chemical derivatization reactions have been used to enhance the desorption/ionization efficiency of selected classes of compounds by adding a functional group with a permanent positive charge or one that can be easily ionized. By utilizing several chemical derivatizations in parallel, metabolite coverage can be drastically improved. This chapter outlines methodology for sample preparation and data analysis for on-tissue chemical derivatization using various derivatization reagents.more » « less
-
Abstract Knowing concentrations of lipids is essential for understanding their physiological functions and discovering new disease biomarkers. However, it is highly challenging to accurately quantify lipids due to structural diversity and multiple isomeric forms of lipids. To address these critical gaps, we have developed a novel aziridine‐based isobaric tag labelling strategy that allows (i) determination of lipid double‐bond positional isomers, (ii) accurate relative quantification of unsaturated lipids, and (iii) improvement of ionization efficiencies of nonpolar lipids. The power of this method is demonstrated in characterization and quantification of various categories of lipids such as fatty acids, phosphoglycerol lipids, cholesteryl esters (CE), and glycerides. 17 CE lipid isomers were identified and quantified simultaneously from Alzheimer's disease (AD) mouse serum without using lipid standards. Among them, 6 CE isomers showed significant changes in concentrations in AD serum.more » « less
-
null (Ed.)Mass spectrometry imaging (MSI) is a powerful, label-free technique that provides detailed maps of hundreds of molecules in complex samples with high sensitivity and subcellular spatial resolution. Accurate quantification in MSI relies on a detailed understanding of matrix effects associated with the ionization process along with evaluation of the extraction efficiency and mass-dependent ion losses occurring in the analysis step. We present a critical summary of approaches developed for quantitative MSI of metabolites, lipids, and proteins in biological tissues and discuss their current and future applications. Expected final online publication date for the Annual Review of Physical Chemistry, Volume 72 is April 2021. Please see http://www.annualreviews.org/page/journal/pubdates for revised estimates.more » « less
-
Abstract Unraveling the complexity of the lipidome requires the development of novel approaches for the structural characterization of lipid species with isomer‐level discrimination. Herein, we introduce an online photochemical approach for lipid isomer identification through selective derivatization of double bonds by reaction with singlet oxygen. Lipid hydroperoxide products are generated promptly after laser irradiation. Fragmentation of these species in a mass spectrometer produces diagnostic fragments revealing the C=C locations in the unreacted lipids. This approach uses an inexpensive light source and photosensitizer making it easy to incorporate into any lipidomics workflow. We demonstrate the utility of this approach for the shotgun profiling of C=C locations in different lipid classes present in tissue extracts using electrospray ionization (ESI) and ambient imaging of lipid species differing only by the location of C=C bonds using nanospray desorption electrospray ionization (nano‐DESI).more » « less
An official website of the United States government
