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ProteomicsPRM of DMXAA-treated Raw264.7 secretome
Raw264.7 cells were cultured in serum-free DMEM containing DMSO or DMXAA for 4 h, and the conditioned media were collected. The precipitated proteins were directly digested with trypsin/Lys-C mix. Three biological replicates of the samples were individually prepared and analyzed by targeted LC-MS/MS...
ORGANISM(S): Mus Musculus (mouse) 
2018-04-04 | PXD009170 | JPOST Repository
ProteomicsSequential Digestion with Different Proteases
We examined three combinations of different proteases for digestion of proteins from TurboID-STING-expressing cells: trypsin alone, Lys-C followed by trypsin, and Glu-C followed by trypsin. First, we tested whether PTS buffer used to solubilize precipitated proteins is compatible with digestion with...
ORGANISM(S): Mus Musculus (mouse) 
2022-08-25 | PXD035242 | JPOST Repository
ProteomicsLFQ_TurboID-STING_anti-biotin_antibody
The STING-null RAW264.7 cells expressing TurboID-STING were treated with DMSO or 30 μg/ml DMXAA, and 500 µM biotin was added to the medium. After 1-h incubation, the cells were lysed in 6 M guanidine-HCl containing 100 mM HEPES-NaOH (pH 7.5), 10 mM TCEP, and 40 mM CAA. The lysates were dissolved by ...
ORGANISM(S): Mus Musculus (mouse) 
2020-06-17 | PXD018803 | JPOST Repository
ProteomicsLFQ_TurboID-STING_Tamavidin2-REV
The STING-null RAW264.7 cells expressing TurboID-STING were treated with DMSO or 30 μg/ml DMXAA, and 500 µM biotin was added to the medium. After 1-h incubation, the cells were lysed in 6 M guanidine-HCl containing 100 mM HEPES-NaOH (pH 7.5), 10 mM TCEP, and 40 mM CAA. The lysates were dissolved by ...
ORGANISM(S): Mus Musculus (mouse) 
2020-06-17 | PXD018802 | JPOST Repository
ProteomicsLFQ of DMXAA-treated Raw264.7 secretome
Raw264.7 cells were cultured in serum-free DMEM containing DMSO or DMXAA for 4 h, and the conditioned medium were collected. The precipitated proteins were directly digested with trypsin. Three biological replicates of the samples were individually prepared and analyzed by LC-MS/MS. Label-free quant...
ORGANISM(S): Mus Musculus (mouse) 
2018-04-04 | PXD009169 | JPOST Repository
ProteomicsOptimization of Elution Conditions for Biotinylated Peptides from Tamavidin 2-REV
We attempted to optimize the conditions for competitive elution of biotinylated peptides from the Tamavidin 2-REV beads. First, to optimize the temperature at which biotinylated peptides were eluted from the beads, biotinylated peptides were eluted with the biotin solution at 4, 37, 56, and 95 ºC. S...
ORGANISM(S): Mus Musculus (mouse) 
2022-08-25 | PXD035219 | JPOST Repository
ProteomicsPurification of Biotinylated Peptides using SDB-SCX StageTip
We tried purification of biotinylated peptides using SDB-SCX StageTip to reduce interference ions. We compared this method with the original and optimized workflows. We assessed reproducibility of each enrichment process by three technical replicates. Original workflow with SDB-SCX: A 15-µL slurry o...
ORGANISM(S): Mus Musculus (mouse) 
2022-08-25 | PXD035229 | JPOST Repository
ProteomicsComparison of Biotinylated Peptides Enriched by the Original and Optimized Workflows using Tamavidin 2-REV.
To evaluate the optimized workflow, biotinylated peptides enriched by the original and optimized workflows from 300 µg proteins of RAW264.7 cells expressing TurboID-STING were compared by LC-MS/MS analysis. We assessed reproducibility of each workflow using six technical replicates. Original workflo...
ORGANISM(S): Mus Musculus (mouse) 
2022-08-25 | PXD035220 | JPOST Repository
ProteomicsReduction of Interference Ions Generated in the Enrichment Process of Biotinylated Peptides using Tamavidin 2-REV
After tryptic digestion of proteins of RAW264.7 cells expressing TurboID-STING, biotinylated peptides were captured with Tamavidin 2-REV magnetic beads and eluted competitively with excess biotin. When the peptide samples were subjected to LC-MS/MS, high intensity peaks of interference and/or contam...
ORGANISM(S): Cellular Organisms Mus Musculus (mouse) 
2022-08-25 | PXD035218 | JPOST Repository
ProteomicsLFQ of GFP-Trap IP-MS from hTBJ1 cells expressing EGFP-mSTING
Permeabilised hTBJ1 cells expressing EGFP-mSTING were stimulated with or without 1 µM 2’3’-cGAMP at 10°C and cross-linked with 0.1 or 0.5% paraformaldehyde at 4°C for 1 h in three independent experiments. After quenching with 100 mM glycine-NaOH, pH 7.5 at 4°C for 15 min, the cells were lysed in RIP...
ORGANISM(S): Homo Sapiens (human) 
2022-12-09 | PXD029736 | JPOST Repository
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