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. 2008 May 30;283(22):15169–15176. doi: 10.1074/jbc.M801229200

FIGURE 7.

FIGURE 7.

The ΔΔβ-toxins do not compete with brevetoxin on binding to site-5. A, locust neuronal membranes were incubated with 0.1 nm 125I-LqhαIT as in Fig. 4. Saturating concentration of PbTx-2 (1 μm; Ref. 19) increased 125I-LqhαIT binding by 30 ± 8%. 0.1 μm ΔΔBj-xtrIT increased 125I-LqhαIT binding (maximal enhancement, Fig. 4) by 172 ± 11%, and in the presence of a mixture of both (1 μm PbTx-2 + 0.1 μm ΔΔBj-xtrIT), the increase in 125I-LqhαIT binding was comparable (168 ± 14%). B, [3H]PbTx-3 binding in the presence of the ΔΔβ-toxins. [3H]PbTx-3 (10 nm) was incubated with rat brain synaptosomes (70 μg) for 3 h at room temperature in the absence (Total binding) or presence of 2 μm PbTx-2 (nonspecific binding) or the indicated concentrations of ΔΔβ-toxins. Identical results were obtained when the ΔΔβ-toxins were preincubated with the membranes for 1 h prior to the addition of [3H]PbTx-3.