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. 2020 May 25;11:1069. doi: 10.3389/fmicb.2020.01069

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.