Quantitative DIA-based proteomic analysis of lysosomes (Lyso-IP) from VPS35[D620N] Mouse Embryonic Fibroblasts (MEFs)
Authors/Creators
- 1. Team Alessi, MRC-PPU, University of Dundee, Dundee, UK
Description
This Zenodo deposit contains a publicly available description of the Dataset:
Title: "Quantitative DIA-based proteomic analysis of lysosomes (Lyso-IP) from VPS35[D620N] Mouse Embryonic Fibroblasts (MEFs)".
Description: Quantitative DIA-based proteomic analysis comparing isolated lysosomes (Lyso-IP) from Wild-Type and VPS35[D620N] knock-in MEFs. This dataset provides the basal characterization of mutant lysosomal protein changes without inhibitor treatment. Expression of the 3XHA-TMEM192 tag was verified by genotyping PCR and anti-HA Western Blotting. Data acquired on an Orbitrap Exploris 480 and processed using DIA-NN 1.8.1.
This dataset is made available to researchers via the ASAP CRN Cloud: cloud.parkinsonsroadmap.org. Instructions for how to request access can be found in the User Manual.
This research was funded by the Aligning Science Across Parkinson's Collaborative Research Network (ASAP CRN), through the Michael J. Fox Foundation for Parkinson's Research (MJFF).
This Zenodo deposit was created by the ASAP CRN Cloud staff on behalf of the dataset authors. It provides a citable reference for a CRN Cloud Dataset
Files
alessi-mefs-ms-p-vps35-d620n-wt_README.pdf
Files
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Additional details
Funding
- Aligning Science Across Parkinson's
- Mapping the LRRK2 signalling pathway and its interplay with other Parkinson’s disease components ASAP-000463
References
- Aligning Science Across Parkinson's Collaborative Research Network Cloud, https://cloud.parkinsonsroadmap.org/collections, RRID:SCR_023923
- Team Alessi