Fig. 5From: A cleavable peptide adapter augments the activity of targeted toxins in combination with the glycosidic endosomal escape enhancer SO1861Cytotoxicity assays of DE and DAES with or without SO1861. Cytotoxicity of DE and DAES was evaluated by incubation of HCT 116 (EGFR-positive) and MDA-MB-453 (low EGFR-expression) cells with different concentrations of the toxins ranging from 0.1 pM to 1 μM, with or without addition of SO1861 at a concentration of 125 μg/mL. After 48 h incubation, the viability of the cells was measured by MTT assay. a1 The curves result from four parameter logistic regression by GraphPad Prism. The 95% confidence interval for each curve is indicated. The displayed data points each represent the mean ± SEM of three or four independent assays each performed in triplicate. As an exception, the two data points of DE at a concentration of 100 nM and 1 μM with addition of SO1861 rely on only two experiments. a2 Overview over IC50-values for HCT 116 cells, including 95% confidence interval and statistical significance. A logarithmic scale is used for the y-axis. Statistical significance was assessed by Student’s unpaired t-test. P < 0.05 was required for statistical significance. P < 0.05, *; P < 0.01, **; P < 0.001, ***. b The curves result from four parameter logistic regression by GraphPad Prism. The 95% confidence intervals could not be calculated because the sigmoid curves did not reach the baseline level due to the low toxicity for MDA-MB-453 cells. The displayed data points each represent the mean ± SEM of three or four independent assays each performed in triplicate. Additional graphs that allow ideal comparison of the effect on HCT 116 cells with the effect on MDA-MB-453 cells can be found in Additional file 8Back to article page