Proteomics

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Labeled quantitative proteomics dataset of optogenetics induced axon regeneration


ABSTRACT: This labeled quantitative proteomics dataset was collected from a transgenic channel rhodopsin mouse model (Chr2) subjected to light stimulation after traumatic optic nerve crush (ONC) was performed. Mouse models expressing channel rhodopsin were subjected to therapeutic light stimulation promoting axon regeneration of retinal ganglion cell (RGC) axons post optic nerve crush. Experimental mice and wild type control mice were euthanized, and optic nerves were collected. A protein extraction was carried out by careful mincing of the tissue in extraction buffer (TEAB, NaCl and SDS). Protein amount normalization across samples was achieved using dot blot densitometry using ImageJ software. Samples were labelled using a modified 16plex TMT (Tandem Mass Tag) kit for quantification after overnight trypsin digestion. Untargeted liquid chromatography-mass spectrometry was performed on an Easy-nLC 1000 liquid chromatograph coupled to a QExactive mass spectrometer (LC-MS/MS). Data analysis was performed using Proteome Discoverer 2.5.

INSTRUMENT(S): Q Exactive

ORGANISM(S): Mus Musculus (mouse)

TISSUE(S): Optic Nerve

DISEASE(S): Disease Free

SUBMITTER: Sanjoy Bhattacharya  

LAB HEAD: Sanjoy K Bhattacharya

PROVIDER: PXD032788 | Pride | 2022-08-12

REPOSITORIES: Pride

Dataset's files

Source:
Action DRS
Optogenetics_TMT_Bio_1.raw Raw
Optogenetics_TMT_Bio_2.raw Raw
Optogenetics_TMT_Bio_3.raw Raw
Optogenetics_TMT_Result_File.mzML Mzml
Optogenetics_TMT_Result_File.mzid.gz Mzid
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Publications

Labeled quantitative proteomics dataset of optogenetics induced axon regeneration in mice.

Harvey Faith Christine FC   Mendoza Ximena X   Liu Yuan Y   Lee Richard K RK   Bhattacharya Sanjoy K SK  

Data in brief 20220521


This labeled quantitative proteomics dataset was collected from a transgenic channel rhodopsin mouse model (Chr2) subjected to light stimulation after traumatic optic nerve crush (ONC). Protein extraction was performed by careful mincing of the tissue in extraction buffer (TEAB, NaCl and SDS). Protein amounts were normalized across samples using dot blot densitometry and ImageJ software. Samples were labeled for quantification using a modified TMTpro™ 16plex Label Reagent Set (Thermo Scientific™  ...[more]

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