AI-driven Deep Visual Proteomics defines cell identity and heterogeneity

The systems-wide analysis of biomolecules in time and space is key to our understanding of cellular function and heterogeneity in health and disease1. Remarkable technological progress in microscopy and multi-omics technologies enable increasingly data-rich descriptions of tissue heterogeneity2,3,4,5. Single cell sequencing, in particular, now routinely allows the mapping of cell types and states uncovering tremendous complexity6. Yet, an unaddressed challenge is the development of a method that would directly connect the visual dimension with the molecular phenotype and in particular with the unbiased characterization of proteomes, a close proxy for cellular function. Here we introduce Deep Visual Proteomics (DVP), which combines advances in artificial intelligence (AI)-driven image analysis of cellular phenotypes with automated single cell laser microdissection and ultra-high sensitivity mass spectrometry7. DVP links protein abundance to complex cellular or subcellular phenotypes while preserving spatial context. Individually excising nuclei from cell culture, we classified distinct cell states with proteomic profiles defined by known and novel proteins. AI also discovered rare cells with distinct morphology, whose potential function was revealed by proteomics. Applied to archival tissue of salivary gland carcinoma, our generic workflow characterized proteomic differences between normal-appearing and adjacent cancer cells, without admixture of background from unrelated cells or extracellular matrix. In melanoma, DVP revealed immune system and DNA replication related prognostic markers that appeared only in specific tumor regions. Thus, DVP provides unprecedented molecular insights into cell and disease biology while retaining spatial information.

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

[2]  Ben C. Collins,et al.  diaPASEF: parallel accumulation–serial fragmentation combined with data-independent acquisition , 2020, Nature Methods.

[3]  M. Krieg,et al.  The nucleus measures shape changes for cellular proprioception to control dynamic cell behavior , 2020, Science.

[4]  Fabian J Theis,et al.  LifeTime and improving European healthcare through cell-based interceptive medicine , 2020, Nature.

[5]  Lassi Paavolainen,et al.  nucleAIzer: A Parameter-free Deep Learning Framework for Nucleus Segmentation Using Image Style Transfer , 2020, Cell systems.

[6]  Marius Pachitariu,et al.  Cellpose: a generalist algorithm for cellular segmentation , 2020, Nature Methods.

[7]  H. Moch,et al.  The single-cell pathology landscape of breast cancer , 2020, Nature.

[8]  S. Preissl,et al.  Single-cell multimodal omics: the power of many , 2020, Nature Methods.

[9]  Method of the Year 2019: Single-cell multimodal omics , 2020, Nature Methods.

[10]  Anne E Carpenter,et al.  Nucleus segmentation across imaging experiments: the 2018 Data Science Bowl , 2019, Nature Methods.

[11]  Matthias Mann,et al.  A streamlined mass spectrometry-based proteomics workflow for large scale FFPE tissue analysis , 2019, bioRxiv.

[12]  Jan Ellenberg,et al.  Integrating Imaging and Omics: Computational Methods and Challenges , 2019, Annual Review of Biomedical Data Science.

[13]  C. Bakal,et al.  The cell-cell adhesion protein JAM3 determines nuclear deformability by regulating microtubule organization , 2019 .

[14]  Roman Fischer,et al.  MaxQuant Software for Ion Mobility Enhanced Shotgun Proteomics* , 2019, Molecular & Cellular Proteomics.

[15]  M. Gurcan,et al.  Digital pathology and artificial intelligence. , 2019, The Lancet. Oncology.

[16]  Anthony J. Cesnik,et al.  Author Correction: Spatiotemporal dissection of the cell cycle with single-cell proteogenomics , 2019, Nature.

[17]  R. Satija,et al.  Integrative single-cell analysis , 2019, Nature Reviews Genetics.

[18]  E. Lundberg,et al.  Spatial proteomics: a powerful discovery tool for cell biology , 2019, Nature Reviews Molecular Cell Biology.

[19]  Damian Szklarczyk,et al.  STRING v11: protein–protein association networks with increased coverage, supporting functional discovery in genome-wide experimental datasets , 2018, Nucleic Acids Res..

[20]  Thomas L. Fillmore,et al.  Residual tissue repositories as a resource for population-based cancer proteomic studies , 2018, Clinical Proteomics.

[21]  Peter Horvath,et al.  Environmental properties of cells improve machine learning-based phenotype recognition accuracy , 2018, Scientific Reports.

[22]  Jeffrey E Gershenwald,et al.  Melanoma staging: Evidence‐based changes in the American Joint Committee on Cancer eighth edition cancer staging manual , 2017, CA: a cancer journal for clinicians.

[23]  Lassi Paavolainen,et al.  Data-analysis strategies for image-based cell profiling , 2017, Nature Methods.

[24]  C. Lindskog,et al.  A pathology atlas of the human cancer transcriptome , 2017, Science.

[25]  Lassi Paavolainen,et al.  Advanced Cell Classifier: User-Friendly Machine-Learning-Based Software for Discovering Phenotypes in High-Content Imaging Data. , 2017, Cell systems.

[26]  Matthias Mann,et al.  Loss-less Nano-fractionator for High Sensitivity, High Coverage Proteomics * , 2017, Molecular & Cellular Proteomics.

[27]  Alexei A. Efros,et al.  Image-to-Image Translation with Conditional Adversarial Networks , 2016, 2017 IEEE Conference on Computer Vision and Pattern Recognition (CVPR).

[28]  Marco Y. Hein,et al.  The Perseus computational platform for comprehensive analysis of (prote)omics data , 2016, Nature Methods.

[29]  M. Ford,et al.  Single‐Cell Transcriptomics Comes of Age , 2016, American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons.

[30]  Yunpeng Li,et al.  CIDRE: an illumination-correction method for optical microscopy , 2015, Nature Methods.

[31]  G. von Heijne,et al.  Tissue-based map of the human proteome , 2015, Science.

[32]  Marco Y. Hein,et al.  Accurate Proteome-wide Label-free Quantification by Delayed Normalization and Maximal Peptide Ratio Extraction, Termed MaxLFQ * , 2014, Molecular & Cellular Proteomics.

[33]  Joshua M. Stuart,et al.  The Cancer Genome Atlas Pan-Cancer analysis project , 2013, Nature Genetics.

[34]  Z. Baloch,et al.  Archived formalin-fixed paraffin-embedded (FFPE) blocks: A valuable underexploited resource for extraction of DNA, RNA, and protein. , 2013, Biopreservation and biobanking.

[35]  Guangchuang Yu,et al.  clusterProfiler: an R package for comparing biological themes among gene clusters. , 2012, Omics : a journal of integrative biology.

[36]  Albert J R Heck,et al.  Trends in ultrasensitive proteomics. , 2012, Current opinion in chemical biology.

[37]  D. Hanahan,et al.  Hallmarks of Cancer: The Next Generation , 2011, Cell.

[38]  X. Kang,et al.  Meiotic chromosome preparation techniques of pollen mother cells for laser micro-dissection in Populus spp. , 2010 .

[39]  Emma Lundberg,et al.  A single fixation protocol for proteome-wide immunofluorescence localization studies. , 2010, Journal of proteomics.

[40]  Jeffrey E Gershenwald,et al.  Final version of 2009 AJCC melanoma staging and classification. , 2009, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[41]  E. Haura,et al.  Src kinases as therapeutic targets for cancer , 2009, Nature Reviews Clinical Oncology.

[42]  M. Mann,et al.  MaxQuant enables high peptide identification rates, individualized p.p.b.-range mass accuracies and proteome-wide protein quantification , 2008, Nature Biotechnology.

[43]  Anne E Carpenter,et al.  CellProfiler: image analysis software for identifying and quantifying cell phenotypes , 2006, Genome Biology.

[44]  S. Green,et al.  Ballistic labeling and dynamic imaging of astrocytes in organotypic hippocampal slice cultures , 2005, Journal of Neuroscience Methods.

[45]  Christine Brun,et al.  In silico prediction of protein-protein interactions in human macrophages , 2001, BMC Research Notes.

[46]  J. Hunt,et al.  Review and updates of immunohistochemistry in selected salivary gland and head and neck tumors. , 2015, Archives of pathology & laboratory medicine.

[47]  Atsushi Miyawaki,et al.  [Visualizing spatiotemporal dynamics of multicellular cell-cycle progression]. , 2012, Seikagaku. The Journal of Japanese Biochemical Society.