TABLE 2.
Differentially expressed mitochondrial proteins in Caco-2 epithelial monolayers after treatment with 10 or 50 μM 3O-C12-HSL for 4 h compared to the diluent control.
| Identified proteins | UniProt accession | MW kDa | P-value emPAI ANOVA | Quantitative profile | Functional groups # | |||||||
| Control | 10 μM | 50 μM | ||||||||||
| Peroxiredoxin-5, mitochondrial | PRDX5_HUMAN | 22 | 0.0024 | Low | High | High | X | |||||
| NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 8 | NDUA8_HUMAN | 20 | 0.011 | Low | High | High | X | |||||
| Periplakin | K7EKI8_HUMAN | 204 | 0.021 | Low | High | High | X | |||||
| Prostaglandin E synthase 2 | PTGES2_HUMAN | 42 | 0.039 | Low | High | High | X | |||||
| Isoform 2 of 39S ribosomal protein L47, mitochondrial | RM47_HUMAN | 27 | 0.041 | High | High | Low | X | |||||
| Peroxisomal bifunctional enzyme | ECHP_HUMAN | 79 | 0.02 | High | Low | High | X | |||||
| Cytochrome c1, heme protein, mitochondrial | CY1_HUMAN | 35 | 0.04 | High | Low | High | X | X | ||||
| Cluster of NAD transhydrogenase | NNTM_HUMAN | 114 | 0.024 | Low | Low | High | X | |||||
| GrpE protein homolog 1, mitochondrial | GRPE1_HUMAN | 24 | 0.034 | Low | Low | High | X | X | ||||
| Cluster of isoform 2 of MICOS complex subunit MIC60 | MIC60_HUMAN | 83 | 0.035 | Low | Low | High | X | |||||
| Stress-70 protein, mitochondrial | GRP75_HUMAN | 74 | 0.041 | Low | Low | High | X | X | ||||
| Succinate–CoA ligase [ADP/GDP-forming] subunit alpha, mitochondrial | SUCA_HUMAN | 36 | 0.0078 | High | Low | Low | X | |||||
| Succinate dehydrogenase assembly factor 2, mitochondrial | F5GYJ5_HUMAN | 18 | 0.0091 | High | Low | Low | X | |||||
| Cytochrome c oxidase subunit 5B, mitochondrial | COX5B_HUMAN | 14 | 0.012 | High | Low | Low | X | |||||
# Functional groups of human proteins: X – respiratory chain complexes; X – cell defense and response to stress and pathogens; X – structural organization; X – lipid metabolism and heme binding; X – chaperone activity; X – ribosomal function. STRING and SCAFFOLD analyses were used to group proteins into functional classes. Data are from six independent experiments.