Abstract

Mass spectrometry imaging (MSI) plays a pivotal role in investigating the chemical nature of complex systems that underly our understanding in biology and medicine. Multiple fields of life science such as proteomics, lipidomics and metabolomics benefit from the ability to simultaneously identify molecules and pinpoint their distribution across a sample. However, achieving the necessary submicron spatial resolution to distinguish chemical differences between individual cells and generating intact molecular spectra is still a challenge with any single imaging approach. Here, we developed an approach that combines two MSI techniques, matrix-assisted laser desorption/ionization (MALDI) and time-of-flight secondary ion mass spectrometry (ToF-SIMS), one with low spatial resolution but intact molecular spectra and the other with nanometer spatial resolution but fragmented molecular signatures, to predict molecular MSI spectra with submicron spatial resolution. The known relationships between the two MSI channels of information are enforced via a physically constrained machine-learning approach and directly incorporated in the data processing. We demonstrate the robustness of this method by generating intact molecular MALDI-type spectra and chemical maps at ToF-SIMS resolution when imaging mouse brain thin tissue sections. This approach can be readily adopted for other types of bioimaging where physical relationships between methods have to be considered to boost the confidence in the reconstruction product.

Highlights

  • Recent developments in mass spectrometry imaging (MSI) have enabled characterization of localized molecular composition in signal transduction[1], drug delivery[2], disease progression[3], and forensics[4]

  • Workflow overview and data collection Overall, the workflow for processing of the coregistered matrix-assisted laser desorption/ionization (MALDI) and ToF-SIMS signals includes the following steps: (1) coregistration of spectral inputs; (2) dimensionality reduction using non-negative matrix factorization (NMF); (3) identification of the physical relations between channels, using canonical correlation analysis (CCA); and (4) reconstruction of molecular mass spectra at high spatial resolution based on a prediction using the identified physical relationship between MALDI and ToF-SIMS channels

  • Following ToF-SIMS analysis and fiducial marker imprinting (Fig. 1c), α-cyano-4-hydroxycinnamic acid (CHCA) matrix was applied by sublimation and MALDI imaging performed with 50-μm pixel size (Fig. 1d)

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Summary

Introduction

Recent developments in mass spectrometry imaging (MSI) have enabled characterization of localized molecular composition in signal transduction[1], drug delivery[2], disease progression[3], and forensics[4]. MSI is an invaluable tool for pharmacological applications that pinpoints spatial distribution of biologically relevant molecules such as proteins[5], peptides[6], lipids[7], and pharmaceuticals[8,9] across the tissue This allows to visualize metabolic processes and generate direct insights into the biological action of novel drug candidates[9]. Potential impact of the ability to generate mass spectra of the intact species will have a pronounced effect on the cellular and subcellular metabolome research[10] This subsequently drives the need for novel analytical tools offering higher sensitivity, and detailed chemical information coupled to high-spatial resolution modes. As the correlation between information channels is assumed but not constrained by any known relationships, the output of such algorithms is prone to reconstruction errors[19]

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