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Leineweber, W. D.

Publications and source records attributed to Leineweber, W. D..

4 recordsLinked to original sources

Generative machine learning unlocks the first proteome-wide image of human cells

The spatial organization of proteins within cells governs virtually all cellular functions, yet current imaging can simultaneously visualize only tens of proteins, orders of magnitude below the thousands populating a single human cell. Here we present ProtiCelli, a deep generative model that simulates microscopy images for 12,800 human proteins from just three cellular landmark stains. Trained on 1.23 million Human Protein Atlas images, ProtiCelli outperforms existing methods in reconstruction accuracy and textural fidelity, and generalizes to unseen cell types and drug perturbations. Simulated images preserve hierarchical subcellular organization, recapitulate known protein protein interaction landscapes, and resolve compartment-specific functions of moonlighting proteins at single cell resolution. Remarkably, the model infers drug-induced changes in protein expression and localization from cell morphology alone, predicts cell cycle stage without dedicated markers, and enables unsupervised segmentation of subcellular compartments and spatial decomposition of gene sets into functional regions. We leverage ProtiCelli to generate Proteome2Cell, a dataset of 30.7 million simulated images spanning 2,400 virtual cells across 12 human cell lines, enabling hierarchical single-cell models that distinguish conserved from dynamic protein architectures. Integrated into the Human Protein Atlas, Proteome2Cell democratizes exploration of these virtual cells. By computationally bridging the experimental scalability gap, ProtiCelli establishes a foundation for spatial virtual cell modeling.

cell biology↗

Cell shapes decode molecular phenotypes in image-basedspatial proteomics

The diversity of cellular and tissue structures can arise from a few basic cell shapes, which undergo various transformations based on biophysical constraints on cytoskeletal organization. While cellular geometry has been linked with selected biological processes such as polarity, signaling or morphogenesis, the orchestration of the whole proteome in association to cell shape is still poorly understood. In this study, using more than 1 million images of single cells stained for 11,998 proteins across 10 cell lines in the Human Protein Atlas database, we performed an integrated analysis of organelle, pathway and single protein levels in association to a 2D cellular shapespace. We found that cell and nuclear shapes across cell lines exist in a shared continuum. We also found that the subcellular organelle topology varies across cell lines, but remains robust within each cell lines shapespace. At the single protein level, we found that cells of different shapes in the same cell cycle phase might be preparing for different fates, and that many non-cell cycle proteins expressed shape-based abundance variation. Using the same coordinate framework defined by shape, we could analyze the distribution shift of protein spatial localization under drug perturbation.

bioengineering↗

SubCell: Vision foundation models for microscopycapture single-cell biology

Cell morphology and subcellular protein organization provide important insights into cellular function and behavior. These cellular features can be studied using large-scale fluorescence microscopy, and machine learning has become a powerful tool to interpret the resulting images for biological insights. Here, we introduce SubCell, a deep learning model for fluorescence microscopy designed to accurately capture cellular morphology, protein localization, cellular forganization, and biological function beyond what humans can readily perceive. SubCell was trained on the proteome-wide image collection from the Human Protein Atlas with a novel proteome-aware learning objective. SubCell outperforms state-of-the-art methods across a variety of tasks relevant to single-cell biology and generalizes to other fluorescence microscopy datasets without any fine-tuning. Additionally, we construct the first proteome-wide hierarchical map of proteome organization that is directly learned from image data. This vision-based multiscale cell map defines cellular subsystems down to protein complex resolution, reveals proteins with similar functions, and distinguishes dynamic and stable behaviors within cellular compartments. Finally, combining SubCell with a protein sequence model enables a rich multimodal approach to capture gene function better than either vision-only or sequence-only models alone. In conclusion, SubCell creates deep, image-driven representations of cellular architecture that are applicable across diverse biological contexts and datasets.

cell biology↗

Holotomographic microscopy reveals label-free quantitative dynamics of endothelial cells during endothelialization

Holotomograhic microscopy (HTM) has emerged as a non-invasive imaging technique that offers high-resolution, quantitative 3D imaging of biological samples. This study explores the application of HTM in examining endothelial cells (ECs). HTM overcomes the limitations of traditional microscopy methods in capturing the real-time dynamics of ECs by leveraging the refractive index (RI) to map 3D distributions label-free. This work demonstrates the utility of HTM in visualizing key cellular processes during endothelialization, wherein ECs anchor, adhere, migrate, and proliferate. Leveraging the high resolution and quantitative power of HTM, we show that lipid droplets and mitochondria are readily visualized, enabling more comprehensive studies on their respective roles during endothelialization. The study highlights how HTM can uncover novel insights into EC behavior, offering potential applications in medical diagnostics and research, particularly in developing treatments for cardiovascular diseases. This advanced imaging technique not only enhances our understanding of EC biology but also presents a significant step forward in the study of cardiovascular diseases, providing a robust platform for future research and therapeutic development.

cell biology↗