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Florian Rosenberger et al., 2023 - in revision

Spatial single-cell mass spectrometry defines zonation of the hepatocyte proteome

Abstract

Single-cell proteomics by mass spectrometry (MS) is emerging as a powerful and unbiased method for the characterization of biological heterogeneity. So far, it has been limited to cultured cells, whereas an expansion of the method to complex tissues would greatly enhance biological insights. Here we describe single-cell Deep Visual Proteomics (scDVP), a technology that integrates high-content imaging, laser microdissection and multiplexed MS. scDVP resolves the context-dependent, spatial proteome of murine hepatocytes at a current depth of 1,700 proteins from a slice of a cell. Half of the proteome was differentially regulated in a spatial manner, with protein levels changing dramatically in proximity to the central vein. We applied machine learning to proteome classes and images, which subsequently inferred the spatial proteome from imaging data alone. scDVP is applicable to healthy and diseased tissues and complements other spatial proteomics or spatial omics technologies.

Liver painting

Table of contents

  1. Data repository
  2. Results
  3. R Scripts
  4. GitHub Notes

Data repository

Processed mass spectrometry raw data and other input files have been saved in the following folders:

Results

Figures and result dataframes are saved in the output folder.

R scripts

Run "_Top_code.R" to execute the entire R code.

Data wrangling scripts

Scripts for main figures

Figure 2, Depth of single shape proteomes and estimation of nuclear compartment

Figure 3, Single shape proteomes are accurate descriptors of zonated hepatocytes

Figure 4, Combining imaging and proteome data for a machine-learned model

Scripts for supplementary figures

Supplementary Figure S1 and S2: Five-shape proteomes

Supplementary Figure S3: Performance overview of single shape proteomes

Supplementary Figure S4: Dimensionality reduction of single shape data

Supplementary Figure S5: Concatentation of shapes

Supplementary Figure S6: Normality checks of single shape data

Supplementart Figure S7

Supplementary Figure S8: Additional data on subcellular localisation

Supplementart Figure S9

GitHub Notes

Clone Repository

Navigate to your local GitHub folder and enter:

>git clone https://github.com/MannLabs/single-cell-DVP.git

Transferring local copy to GitHUb

Update current status:

#git pull https://github.com/MannLabs/single-cell-DVP.git

Push changes by indicating the date of change and editor (e.g.: Florian Rosenberger on Feb 20 e.g. 20230220_FR)

  1. Get the path of you local GitHub folder

P:\03_Experiments\24_Borderline_Project\18_Github\Borderline_Manuscript>git init

  1. Add files and commit changes:

>git add .

>git commit -m "20230220_Editor"

>git remote -v

>git push origin main

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