Integrative Multiscale Biochemical Mapping of the Brain via Deep-Learning-Enhanced High-Throughput Mass Spectrometry

Elucidating the spatial-biochemical organization of the brain across different scales produces invaluable insight into the molecular intricacy of the brain. While mass spectrometry imaging (MSI) provides spatial localization of compounds, comprehensive chemical profiling of large brain regions in three dimensions by MSI with single-cell resolution has not been achieved. We demonstrate complementary brain-wide and single-cell biochemical mapping via MEISTER, an integrative experimental and computational mass spectrometry framework. MEISTER integrates a deep-learning-based reconstruction that accelerates high-mass-resolving MS by 15-fold, multimodal registration creating 3D molecular distribution, and a data integration method fitting cell-specific mass spectra to 3D data sets. We imaged detailed lipid profiles in tissues with data sets containing millions of pixels, and in large single-cell populations acquired from the rat brain. We identified region-specific lipid contents, and cell-specific localizations of lipids depending on both cell subpopulations and anatomical origins of the cells. Our workflow establishes a blueprint for future developments of multiscale technologies for biochemical characterization of the brain.

[1]  Milad R. Vahid,et al.  High-resolution alignment of single-cell and spatial transcriptomes with CytoSPACE , 2023, Nature Biotechnology.

[2]  Brian R. Long,et al.  A high-resolution transcriptomic and spatial atlas of cell types in the whole mouse brain , 2023, bioRxiv.

[3]  S. Aerts,et al.  Mitochondria metabolism sets the species-specific tempo of neuronal development , 2023, Science.

[4]  M. Eisenstein Seven technologies to watch in 2023 , 2023, Nature.

[5]  F. W. Townes,et al.  Nonnegative spatial factorization applied to spatial genomics , 2022, Nature Methods.

[6]  Dong Hye Ye,et al.  High-Throughput Mass Spectrometry Imaging with Dynamic Sparse Sampling , 2022, ACS measurement science Au.

[7]  A. Brunner,et al.  Deep Visual Proteomics defines single-cell identity and heterogeneity , 2022, Nature Biotechnology.

[8]  K. Qu,et al.  Benchmarking spatial and single-cell transcriptomics integration methods for transcript distribution prediction and cell type deconvolution , 2022, Nature Methods.

[9]  Andrew P. Bowman,et al.  Sphingolipids control dermal fibroblast heterogeneity , 2022, Science.

[10]  Lynette R. Bower,et al.  A metabolome atlas of the aging mouse brain , 2021, Nature Communications.

[11]  Daniel C. Castro,et al.  Enhancing the Throughput of FT Mass Spectrometry Imaging Using Joint Compressed Sensing and Subspace Modeling. , 2021, Analytical chemistry.

[12]  Elizabeth C. Randall,et al.  Peak learning of mass spectrometry imaging data using artificial neural networks , 2021, Nature Communications.

[13]  Gustavo S. França,et al.  Exploring tissue architecture using spatial transcriptomics , 2021, Nature.

[14]  Zheng-Jiang Zhu,et al.  Ion mobility-based sterolomics reveals spatially and temporally distinctive sterol lipids in the mouse brain , 2021, Nature Communications.

[15]  P. Khavari,et al.  Integrating single-cell and spatial transcriptomics to elucidate intercellular tissue dynamics , 2021, Nature Reviews Genetics.

[16]  P. Timpson,et al.  Automated annotation and visualisation of high-resolution spatial proteomic mass spectrometry imaging data using HIT-MAP , 2021, Nature Communications.

[17]  M. Heikenwalder,et al.  SpaceM reveals metabolic states of single cells , 2021, Nature Methods.

[18]  Fabian J Theis,et al.  Ultra‐high sensitivity mass spectrometry quantifies single‐cell proteome changes upon perturbation , 2020, bioRxiv.

[19]  Lu Fang,et al.  Reinforcing neuron extraction and spike inference in calcium imaging using deep self-supervised learning , 2020, bioRxiv.

[20]  Christof Koch,et al.  Removing independent noise in systems neuroscience data using DeepInterpolation , 2020, bioRxiv.

[21]  Daniel Coelho de Castro,et al.  Accelerating Fourier Transform-Ion Cyclotron Resonance Mass Spectrometry Imaging Using a Subspace Approach. , 2020, Journal of the American Society for Mass Spectrometry.

[22]  Long N Nguyen,et al.  Emerging roles of lysophospholipids in health and disease. , 2020, Progress in lipid research.

[23]  Tim Sainburg,et al.  Parametric UMAP Embeddings for Representation and Semisupervised Learning , 2020, Neural Computation.

[24]  M. Mann,et al.  Cell-Type- and Brain-Region-Resolved Mouse Brain Lipidome. , 2020, Cell reports.

[25]  Hongkui Zeng,et al.  A taxonomy of transcriptomic cell types across the isocortex and hippocampal formation , 2020, Cell.

[26]  Ryan T. Kelly,et al.  Automated mass spectrometry imaging of over 2000 proteins from tissue sections at 100-μm spatial resolution , 2020, Nature Communications.

[27]  N. Friedman,et al.  Gene expression cartography , 2019, Nature.

[28]  S. Hasselbalch,et al.  Ageing as a risk factor for neurodegenerative disease , 2019, Nature Reviews Neurology.

[29]  David H Perlman,et al.  Single-cell proteomic and transcriptomic analysis of macrophage heterogeneity using SCoPE2 , 2019, Genome Biology.

[30]  Fan Zhang,et al.  Fast, sensitive, and accurate integration of single cell data with Harmony , 2018, bioRxiv.

[31]  R. Caprioli,et al.  Advanced Registration and Analysis of MALDI Imaging Mass Spectrometry Measurements through Autofluorescence Microscopy. , 2018, Analytical chemistry.

[32]  Elizabeth K. Neumann,et al.  Multimodal Chemical Analysis of the Brain by High Mass Resolution Mass Spectrometry and Infrared Spectroscopic Imaging. , 2018, Analytical chemistry.

[33]  K. Schwamborn,et al.  Mass Spectrometry Imaging and Integration with Other Imaging Modalities for Greater Molecular Understanding of Biological Tissues , 2018, Molecular Imaging and Biology.

[34]  Morgan R Alexander,et al.  The 3D OrbiSIMS—label-free metabolic imaging with subcellular lateral resolution and high mass-resolving power , 2017, Nature Methods.

[35]  Michael Becker,et al.  FDR-controlled metabolite annotation for high-resolution imaging mass spectrometry , 2016, Nature Methods.

[36]  Bernhard Spengler,et al.  Atmospheric pressure MALDI mass spectrometry imaging of tissues and cells at 1.4-μm lateral resolution , 2016, Nature Methods.

[37]  S. Quake,et al.  A survey of human brain transcriptome diversity at the single cell level , 2015, Proceedings of the National Academy of Sciences.

[38]  D. Piomelli,et al.  Peripheral gating of pain signals by endogenous lipid mediators , 2014, Nature Neuroscience.

[39]  A. Gambin,et al.  BRAIN: a universal tool for high-throughput calculations of the isotopic distribution for mass spectrometry. , 2013, Analytical chemistry.

[40]  Allan R. Jones,et al.  An anatomically comprehensive atlas of the adult human brain transcriptome , 2012, Nature.

[41]  J. Sweedler,et al.  Profiling metabolites and peptides in single cells , 2011, Nature Methods.

[42]  Eoin Fahy,et al.  LIPID MAPS online tools for lipid research , 2007, Nucleic Acids Res..

[43]  J. Milbrandt,et al.  Lipid rafts in neuronal signaling and function , 2002, Trends in Neurosciences.

[44]  A. Marshall,et al.  Relaxation and spectral line shape in Fourier transform ion resonance spectroscopy , 1979 .

[45]  Benoit M Dawant,et al.  Integrating spatially resolved three-dimensional MALDI IMS with in vivo magnetic resonance imaging , 2008, Nature Methods.