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. 2024 Jan 9;300(2):105626. doi: 10.1016/j.jbc.2024.105626

Figure S3.

Figure S3

N24A and R30A mutations of CI accessory subunit NDUFB4 modify cellular metabolism and substrate preference. A, the rate of ATP formation from OXPHOS and glycolysis and OXPHOS, n = 3 (B) The glycolytic index, n = 3 from independent experiments. C, confocal microscopy of cells stained with TOMM20 and nuclei (Hoechst). D–F, enzymatic activity of (D) Citrate synthase, (E) Lactate dehydrogenase (LDH), and (F) Malate dehydrogenase, n = 6-7 biological replicates. G, contributions of N-linked respiration and S-linked respiration in the co-stimulated protocol, n = 5-6 from independent experiments. H and I, catalytic activity of (H) Complex I (CI) and (I) Complex II, n = 6-7 biological replicates. (J) Steady-state CoQ10 levels, n = 7-9 biological replicates. Values are Means ± SEM. Comparisons between groups were determined using a one-way ANOVA with Tukey post-hoc test. ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, ∗∗∗∗p < 0.0001.