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  Deep and fast label-free Dynamic Organellar Mapping

Schessner, J. P., Albrecht, V., Davies, A. K., Sinitcyn, P., & Borner, G. H. H. (2023). Deep and fast label-free Dynamic Organellar Mapping. Nature Communications, 14(1): 5252. doi:10.1038/s41467-023-41000-7.

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 Creators:
Schessner, Julia P.1, 2, Author           
Albrecht, Vincent1, 2, Author           
Davies, Alexandra K.1, 2, Author           
Sinitcyn, Pavel3, Author           
Borner, Georg H. H.1, 2, Author           
Affiliations:
1Borner, Georg / Systems Biology of Membrane Trafficking, Max Planck Institute of Biochemistry, Max Planck Society, ou_3060205              
2Mann, Matthias / Proteomics and Signal Transduction, Max Planck Institute of Biochemistry, Max Planck Society, ou_1565159              
3Cox, Jürgen / Computational Systems Biochemistry, Max Planck Institute of Biochemistry, Max Planck Society, ou_2063284              

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Free keywords: PROTEIN LOCALIZATION; COMPUTATIONAL PLATFORM; MESSENGER-RNA; CELL-SURFACE; PROTEOMICS; QUANTIFICATION; INITIATION; COMPLEXES; AUTOPHAGY; MIXTURESScience & Technology - Other Topics;
 Abstract: 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.

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Language(s): eng - English
 Dates: 2023-08-29
 Publication Status: Published online
 Pages: 19
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Degree: -

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Title: Nature Communications
  Abbreviation : Nat. Commun.
Source Genre: Journal
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Publ. Info: London : Nature Publishing Group
Pages: - Volume / Issue: 14 (1) Sequence Number: 5252 Start / End Page: - Identifier: ISSN: 2041-1723
CoNE: https://pure.mpg.de/cone/journals/resource/2041-1723