Deep and fast label-free Dynamic Organellar Mapping.
Julia Patricia SchessnerVincent AlbrechtAlexandra K DaviesPavel SinitcynGeorg H H BornerPublished in: Nature communications (2023)
The Dynamic Organellar Maps (DOMs) approach combines cell fractionation and shotgun-proteomics for global profiling analysis of protein subcellular localization. Here, we enhance the performance of DOMs through data-independent acquisition (DIA) mass spectrometry. DIA-DOMs achieve twice the depth of our previous workflow in the same mass spectrometry runtime, and substantially improve profiling precision and reproducibility. We leverage this gain to establish flexible map formats scaling from high-throughput analyses to extra-deep coverage. Furthermore, we introduce DOM-ABC, a powerful and user-friendly open-source software tool for analyzing profiling data. We apply DIA-DOMs to capture subcellular localization changes in response to starvation and disruption of lysosomal pH in HeLa cells, which identifies a subset of Golgi proteins that cycle through endosomes. An imaging time-course reveals different cycling patterns and confirms the quantitative predictive power of our translocation analysis. DIA-DOMs offer a superior workflow for label-free spatial proteomics as a systematic phenotype discovery tool.
Keyphrases
- label free
- single cell
- high resolution
- mass spectrometry
- high throughput
- electronic health record
- liquid chromatography
- cell cycle arrest
- induced apoptosis
- big data
- data analysis
- small molecule
- high performance liquid chromatography
- high density
- capillary electrophoresis
- cell death
- genome wide
- healthcare
- optical coherence tomography
- stem cells
- high intensity
- dna methylation
- bone marrow
- binding protein
- artificial intelligence
- signaling pathway
- machine learning
- gene expression
- pi k akt
- mesenchymal stem cells
- tandem mass spectrometry
- oxidative stress
- photodynamic therapy