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. 2010 Jun 16;98(12):2770–2779. doi: 10.1016/j.bpj.2010.03.051

Figure 4.

Figure 4

Cytosolic concentration profiles of β-catenin (A), α-catenin (B), and α-catenin dimers (C) resulting from the reaction-diffusion system described by Eqs. 1a–1d, with the boundary conditions without cell-cell contact (Eq. 6) or with cell-cell contact (Eq. 7), as functions of the distance from the center of a cell with spherical symmetry. The different parameters are as follows. The Golgi apparatus of the cell is located at r0 = 1 μm and the total radius of the cell is R = 10 μm. The β-catenin influx is j0β = 5.0 μm μM s−1. The diffusion constants of α- and β-catenin are equal to 1 μm2 s−1, and the one for α-catenin dimers is 0.5 μm2 s−1 (30). In these plots, the reaction rate of α-catenin with β-catenin is 0.01 μM−1 s−1, and that of α-catenin with itself is 0.005 μM−1 s−1 (31). The protein degradation rates of α-catenin and β-catenin are equal to 10−3 s−1, and the consumption and degradation rates of α-catenin dimers are 0.5 × 10−3 s−1. Finally, the membrane binding and unbinding rates, konβ and koffβ, of the β-catenin protein complex are equal to 1 μm s−1 and 1 s−1, respectively.