| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-111 |
Sentence |
denotes |
Global Analysis of Protein Expression and Phosphorylation Levels in Nicotine-Treated Pancreatic Stellate Cells. |
| T1 |
0-111 |
Sentence |
denotes |
Global Analysis of Protein Expression and Phosphorylation Levels in Nicotine-Treated Pancreatic Stellate Cells. |
| TextSentencer_T2 |
112-269 |
Sentence |
denotes |
Smoking is a risk factor in pancreatic disease; however, the biochemical mechanisms correlating smoking with pancreatic dysfunction remain poorly understood. |
| T2 |
112-269 |
Sentence |
denotes |
Smoking is a risk factor in pancreatic disease; however, the biochemical mechanisms correlating smoking with pancreatic dysfunction remain poorly understood. |
| TextSentencer_T3 |
270-409 |
Sentence |
denotes |
Strategies using multiplexed isobaric tag-based mass spectrometry facilitate the study of drug-induced perturbations on biological systems. |
| T3 |
270-409 |
Sentence |
denotes |
Strategies using multiplexed isobaric tag-based mass spectrometry facilitate the study of drug-induced perturbations on biological systems. |
| TextSentencer_T4 |
410-644 |
Sentence |
denotes |
Here, we present the first large-scale analysis of the proteomic and phosphoproteomic alterations in pancreatic stellate cells following treatment with two nicotinic acetylcholine receptor (nAChR) ligands: nicotine and α-bungarotoxin. |
| T4 |
410-644 |
Sentence |
denotes |
Here, we present the first large-scale analysis of the proteomic and phosphoproteomic alterations in pancreatic stellate cells following treatment with two nicotinic acetylcholine receptor (nAChR) ligands: nicotine and α-bungarotoxin. |
| TextSentencer_T5 |
645-863 |
Sentence |
denotes |
We treated cells with nicotine or α-bungarotoxin for 12 h in triplicate and compared alterations in protein expression and phosphorylation levels to mock-treated cells using a tandem mass tag (TMT9plex)-based approach. |
| T5 |
645-863 |
Sentence |
denotes |
We treated cells with nicotine or α-bungarotoxin for 12 h in triplicate and compared alterations in protein expression and phosphorylation levels to mock-treated cells using a tandem mass tag (TMT9plex)-based approach. |
| TextSentencer_T6 |
864-991 |
Sentence |
denotes |
Over 8100 proteins were quantified across all nine samples, of which 46 were altered in abundance upon treatment with nicotine. |
| T6 |
864-991 |
Sentence |
denotes |
Over 8100 proteins were quantified across all nine samples, of which 46 were altered in abundance upon treatment with nicotine. |
| TextSentencer_T7 |
992-1143 |
Sentence |
denotes |
Proteins with increased abundance included those associated with neurons, defense mechanisms, indicators of pancreatic disease, and lysosomal proteins. |
| T7 |
992-1143 |
Sentence |
denotes |
Proteins with increased abundance included those associated with neurons, defense mechanisms, indicators of pancreatic disease, and lysosomal proteins. |
| TextSentencer_T8 |
1144-1364 |
Sentence |
denotes |
In addition, we measured differences for ∼16 000 phosphorylation sites across all nine samples using a titanium dioxide-based strategy, of which 132 sites were altered with nicotine and 451 with α-bungarotoxin treatment. |
| T8 |
1144-1364 |
Sentence |
denotes |
In addition, we measured differences for ∼16 000 phosphorylation sites across all nine samples using a titanium dioxide-based strategy, of which 132 sites were altered with nicotine and 451 with α-bungarotoxin treatment. |
| TextSentencer_T9 |
1365-1461 |
Sentence |
denotes |
Many altered phosphorylation sites were involved in nuclear function and transcriptional events. |
| T9 |
1365-1461 |
Sentence |
denotes |
Many altered phosphorylation sites were involved in nuclear function and transcriptional events. |
| TextSentencer_T10 |
1462-1640 |
Sentence |
denotes |
This study supports the development of future targeted investigations to establish a better understanding for the role of nicotine and associated receptors in pancreatic disease. |
| T10 |
1462-1640 |
Sentence |
denotes |
This study supports the development of future targeted investigations to establish a better understanding for the role of nicotine and associated receptors in pancreatic disease. |