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Research Article

Inhibition of anthrax lethal factor by curcumin and chemically modified curcumin derivatives

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Pages 663-669 | Received 17 Jul 2013, Accepted 20 Aug 2013, Published online: 09 Oct 2013

Figures & data

Figure 1. Molecular structures of Compounds 15.

Figure 1. Molecular structures of Compounds 1–5.

Figure 2. (A) Lethal factor activity as measured by fluorescence generated over time. 100 nM lethal factor, 3 μM substrate and 20 μM inhibitors were used uniformly. Assay buffer was used in place of inhibitor as a control. (B) Percent residual activity of 100 nM lethal factor and 3 μM substrate after incubation with 20 μM inhibitors. All experiments were performed in triplicate. R2 values for all data exceeded 0.99, as determined by Levenberg–Marquardt linear regression analysis, indicating a high level of goodness-of-fit.

Figure 2. (A) Lethal factor activity as measured by fluorescence generated over time. 100 nM lethal factor, 3 μM substrate and 20 μM inhibitors were used uniformly. Assay buffer was used in place of inhibitor as a control. (B) Percent residual activity of 100 nM lethal factor and 3 μM substrate after incubation with 20 μM inhibitors. All experiments were performed in triplicate. R2 values for all data exceeded 0.99, as determined by Levenberg–Marquardt linear regression analysis, indicating a high level of goodness-of-fit.

Figure 3. Lineweaver–Burk and Dixon plots of 100 nM lethal factor activity over four substrate concentrations and four inhibitor concentrations. (A) Lineweaver–Burk plot for Compound 1, (B) Lineweaver–Burk plot for Compound 3, (C) Dixon plot for Compound 1 and (D) Dixon plot for Compound 3.

Figure 3. Lineweaver–Burk and Dixon plots of 100 nM lethal factor activity over four substrate concentrations and four inhibitor concentrations. (A) Lineweaver–Burk plot for Compound 1, (B) Lineweaver–Burk plot for Compound 3, (C) Dixon plot for Compound 1 and (D) Dixon plot for Compound 3.
Supplemental material

Supplementary Material

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