In addition, liquid chromatography mass spectrometry (LC-MS/MS) proteomic analysis was performed as previously described30 (link),31 (link). EV pellets were solubilized and lysed, and protein samples denatured. Aliquots were resolubilized in reducing sample buffer and samples electrophoresed. Gel sections were digested with trypsin31 (link), and peptides extracted and transferred onto a PicoFrit column 9 (NewObjective), self-packed with Agilent Poroshell 120 S 2.7 µm EC-C18 stationary phase, using a Dionex UltiMate 3000 RSLC LC system (Thermo-Fisher Scientific). Peptides were separated and eluting peptides analyzed using a QExactive mass spectrometer (Thermo-Fisher Scientific).
mRNA Sequencing and Proteomic Analysis of MSC-derived EVs
In addition, liquid chromatography mass spectrometry (LC-MS/MS) proteomic analysis was performed as previously described30 (link),31 (link). EV pellets were solubilized and lysed, and protein samples denatured. Aliquots were resolubilized in reducing sample buffer and samples electrophoresed. Gel sections were digested with trypsin31 (link), and peptides extracted and transferred onto a PicoFrit column 9 (NewObjective), self-packed with Agilent Poroshell 120 S 2.7 µm EC-C18 stationary phase, using a Dionex UltiMate 3000 RSLC LC system (Thermo-Fisher Scientific). Peptides were separated and eluting peptides analyzed using a QExactive mass spectrometer (Thermo-Fisher Scientific).
Corresponding Organization : WinnMed
Other organizations : Mayo Clinic in Arizona
Protocol cited in 2 other protocols
Variable analysis
- MRNA isolation method (mirVana PARIS total RNA isolation kit)
- MRNA expression levels (RPKM)
- Protein expression levels (from LC-MS/MS)
- Sequencing method (Illumina HiSeq 2000, TruSeq SBS kit version 3)
- Data analysis method (MAPRSeq v.1.2.1, TopHat 2.0.6, featureCounts)
- Protein sample preparation (solubilization, denaturation, gel electrophoresis, trypsin digestion)
- Positive control: Not specified
- Negative control: Not specified
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