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. 2011 Aug 8;286(39):34088–34100. doi: 10.1074/jbc.M111.243907

FIGURE 3.

FIGURE 3.

The interaction of oligomeric Aβ42 with different proteins followed by ELISA. A, the plate was coated with 0.5 μg/well TPPP/p25 (▴), tubulin (○), or α-synuclein (●), then it was incubated with Aβ42 at different concentrations. B, the apparent dissociation constants (Kd) characteristic for the interactions were evaluated by non-linear fitting of the hyperbolic saturation curves using the Microcal Origin 6.0 software. C, ○, the plate was coated with TPPP/p25 then incubated with Aβ42. After incubation, tubulin was added in constant concentration (100 nm). After further incubation, anti-tubulin was added. ●, the plate was coated with TPPP/p25 and incubated with Aβ42, 100 nm α-synuclein was added, and then anti-α-synuclein was added. The effect of the Aβ42 was calculated as the absorbance at a given Aβ42 concentration divided by the absorbance without Aβ42. D, ○, the plate was coated with α-synuclein, then incubated with Aβ42. After incubation, tubulin was added in constant concentration (100 nm). After further incubation, anti-tubulin was added. The average of three-five independent experiments and the S.E. is shown.