Peptides from Extruded Lupin (Lupinus albus L.) Regulate Inflammatory Activity via the p38 MAPK Signal Transduction Pathway in RAW 264.7 Cells.
Yue GaoXuna ZhangGuixing RenCai-E WuPeiyou QinYang YaoPublished in: Journal of agricultural and food chemistry (2020)
In this study, protein was extracted from extruded lupin and submitted to gastroduodenal digests to obtain lupin peptides, which were characterized using ultraperformance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS). After this, IQDKEGIPPDQQR (IQD), the lupine peptide monomer characterized after UPLC-MS/MS, was screened out by macrophage inflammatory cytokine production assay. RNA-sequencing analysis was performed to explore the mechanisms underlying the anti-inflammatory activity associated with this peptide. The results indicated that lupin peptides effectively inhibited the lipopolysaccharide-induced overproduction of proinflammatory mediators. IQD inhibited the production of tumor necrosis factor-α, interleukin (IL)-6, IL-1β, and monocyte chemoattractant protein-1 by 51.20, 38.52, 44.70, and 40.43%, respectively. RNA-sequencing results showed that IQD inhibited the inflammatory response by regulating the gene expression of the p38 mitogen-activated protein kinase pathway and inhibiting downstream inflammatory cytokines. These bioactive peptides may be used to develop new ingredients for anti-inflammatory nutritional supplements.
Keyphrases
- liquid chromatography tandem mass spectrometry
- simultaneous determination
- ms ms
- lipopolysaccharide induced
- inflammatory response
- amino acid
- gene expression
- single cell
- solid phase extraction
- anti inflammatory
- high performance liquid chromatography
- induced apoptosis
- oxidative stress
- tandem mass spectrometry
- ultra high performance liquid chromatography
- lps induced
- toll like receptor
- rheumatoid arthritis
- dna methylation
- signaling pathway
- high throughput
- liquid chromatography
- protein protein
- molecularly imprinted
- cell cycle arrest
- cell death
- binding protein
- mass spectrometry
- small molecule
- cell proliferation
- immune response
- protein kinase