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Single-nucleus proteomics identifies regulators of protein transport

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Demonstrated aim:

This work demonstrated an approach to infer novel functional regulators from (sub-)single-cell proteomics data. Specifically, the natural proteomic and functional variability of THP-1 macrophage-like cells was used to identify regulators of LPS-induced nucleocytoplasmic protein transport. Cells were treated with LPS for short durations (10, 30, or 60 minutes) or left not-treated.

 

Methods:

Bulk data:

Proteomics method: plexDIA
Sample preparation method: mPOP  

Single-nucleus data:

Proteomics method: SCoPE-DIA
Sample preparation method: nPOP

 

Data organized by experiments

All processed data from the article are organized in this directory.

Meta data for mapping single-nuclei and bulk data are here

 

Raw data and search results from DIA-NN

The repository below contains raw mass-spectrometry data files generated by a timsTOF SCP as well as the search results from analyzing the raw files by DIA-NN (v.1.8.1).

 

Repeating the computational analyses:

The {targets} R package was used to ensure repeatability of our analyses. R scripts corresponding to bulk, single nucleus, and knock down data can be found in the "Code" folder of our Github. The DIA-NN outputs can be found in our MassIVE repository; meta data, and other misc files required to run the code can be found in our directory

 

 

 

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