2020
DOI: 10.1016/j.foodchem.2020.127133
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TMT-based quantitative proteomic analysis of porcine muscle associated with postmortem meat quality

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Cited by 56 publications
(35 citation statements)
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“…Since there was no difference in fiber types in breast muscle, the higher shear force and lower pressing loss in SG meat than in FG meat may be attributed to the larger muscle fibers with less extracellular space in the former. Similar results were obtained for pork; the muscle fibers of meat with a high drip loss were much smaller and less closely aligned than meat with a low drip loss ( Hou et al, 2020 ). People in China tend to judge poultry products with high pigments as prolonged raising cycle meat with high nutrient levels.…”
Section: Discussionsupporting
confidence: 76%
“…Since there was no difference in fiber types in breast muscle, the higher shear force and lower pressing loss in SG meat than in FG meat may be attributed to the larger muscle fibers with less extracellular space in the former. Similar results were obtained for pork; the muscle fibers of meat with a high drip loss were much smaller and less closely aligned than meat with a low drip loss ( Hou et al, 2020 ). People in China tend to judge poultry products with high pigments as prolonged raising cycle meat with high nutrient levels.…”
Section: Discussionsupporting
confidence: 76%
“…The quantitative analysis of proteomic protein was conducted using TMT labeling method. The protein digestion was performed as described by Hou et al [ 48 ]. Briefly, dithiothreitol was firstly added into 100 μg of extracted protein with 25 mM final concentration and incubated at 37 °C for 1 h. Then, iodoacetamide with 50 mM final concentration was added and incubated in darkness at room temperature for 30 min.…”
Section: Methodsmentioning
confidence: 99%
“…The labeled samples were pooled in equal proportion and subjected to nano-liquid chromatography–tandem mass spectrometry (nanoLC–MS/MS). NanoLC–MS/MS analysis was performed on an Orbitrap Fusion Tribrid MS (Thermo, Waltham, MA) equipped with an UltiMate 3000 system according to the procedure described by Hou et al [ 48 ]. The collected raw MS/MS data were processed using Maxquant proteomics software (Version 1.6.4) against UniProt proteomes of Peniophora genus.…”
Section: Methodsmentioning
confidence: 99%
“…(ii) TMTpro labeling. Two sets of TMTpro Plex amine-reactive reagents were used to label 30 samples ( 46 ). Channel 126 was used to label an equally proportioned sample as the reference channel.…”
Section: Methodsmentioning
confidence: 99%