| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-162 |
Sentence |
denotes |
Highly reproducible improved label-free quantitative analysis of cellular phosphoproteome by optimization of LC-MS/MS gradient and analytical column construction. |
| T1 |
0-162 |
Sentence |
denotes |
Highly reproducible improved label-free quantitative analysis of cellular phosphoproteome by optimization of LC-MS/MS gradient and analytical column construction. |
| TextSentencer_T2 |
163-313 |
Sentence |
denotes |
Expanding the sequencing depth of the peptides with a statistically significant quantitative change derived from a biological stimulation is critical. |
| T2 |
163-313 |
Sentence |
denotes |
Expanding the sequencing depth of the peptides with a statistically significant quantitative change derived from a biological stimulation is critical. |
| TextSentencer_T3 |
314-487 |
Sentence |
denotes |
Here we demonstrate that optimization of LC gradient and analytical column construction can reveal over 30,000 unique peptides and 23,000 phosphopeptides at high confidence. |
| T3 |
314-487 |
Sentence |
denotes |
Here we demonstrate that optimization of LC gradient and analytical column construction can reveal over 30,000 unique peptides and 23,000 phosphopeptides at high confidence. |
| TextSentencer_T4 |
488-665 |
Sentence |
denotes |
The quantitative reproducibility of different analytical workflows was evaluated by comparing the phosphoproteome of CD3/4 stimulated and unstimulated T-cells as a model system. |
| T4 |
488-665 |
Sentence |
denotes |
The quantitative reproducibility of different analytical workflows was evaluated by comparing the phosphoproteome of CD3/4 stimulated and unstimulated T-cells as a model system. |
| TextSentencer_T5 |
666-869 |
Sentence |
denotes |
A fritless, 50cm-long column packed with 1.9μm particles operated with a standard pressure HPLC significantly improved the sequencing depth 51% and decreased the selected ion chromatogram peak spreading. |
| T5 |
666-869 |
Sentence |
denotes |
A fritless, 50cm-long column packed with 1.9μm particles operated with a standard pressure HPLC significantly improved the sequencing depth 51% and decreased the selected ion chromatogram peak spreading. |
| TextSentencer_T6 |
870-1067 |
Sentence |
denotes |
Most importantly, under the optimal workflow we observed an improvement of over 300% in detection of significantly changed phosphopeptides in the stimulated cells compared with the other workflows. |
| T6 |
870-1067 |
Sentence |
denotes |
Most importantly, under the optimal workflow we observed an improvement of over 300% in detection of significantly changed phosphopeptides in the stimulated cells compared with the other workflows. |
| TextSentencer_T7 |
1068-1388 |
Sentence |
denotes |
The discovery power of the optimized column configuration was illustrated by identification of significantly altered phosphopeptides harboring novel sites from proteins previously established as important in T cell signaling including A-Raf, B-Raf, c-Myc, CARMA1, Fyn, ITK, LAT, NFAT1/2/3, PKCα, PLCγ1/2, RAF1, and SOS1. |
| T7 |
1068-1388 |
Sentence |
denotes |
The discovery power of the optimized column configuration was illustrated by identification of significantly altered phosphopeptides harboring novel sites from proteins previously established as important in T cell signaling including A-Raf, B-Raf, c-Myc, CARMA1, Fyn, ITK, LAT, NFAT1/2/3, PKCα, PLCγ1/2, RAF1, and SOS1. |
| TextSentencer_T8 |
1389-1663 |
Sentence |
denotes |
Taken together, our results reveal the analytical power of optimized chromatography using sub 2μm particles for the analysis of the T cell phosphoproteome to reveal a vast landscape of significantly altered phosphorylation changes in response to T cell receptor stimulation. |
| T8 |
1389-1663 |
Sentence |
denotes |
Taken together, our results reveal the analytical power of optimized chromatography using sub 2μm particles for the analysis of the T cell phosphoproteome to reveal a vast landscape of significantly altered phosphorylation changes in response to T cell receptor stimulation. |