Two examples of the enzymatic flux, J, as a function of the substrate concentration, [S], for Michaelis-Menten kinetics (Equation 6.1). Arbitrary units are used and Vmax = 1. Black line: Km = 0.5. Blue line: Km = 2. Note that half-maximal flux occurs when [S] = Km.
Figure 6.all
Calcium transients in a 1.0 single cylindrical compartment, 1 μm in diameter and 1 μm in length (similar in size to a spine head). Initial concentration is 0.05 μM. Influx is due to a calcium current of 5 μA cm−2, starting at 20 ms for 2 ms, across the radial surface. Black line: accumulation of calcium with no decay or extrusion. Blue line: simple decay with τdec = 27 ms. Gray dashed line: instantaneous pump with Vpump = 4 × 10−6 μMs−1, equivalent to 10−11 mol cm−2 s−1 through the surface area of this compartment, Kpump = 10 μM, Jleak = 0.0199 × 10−6 μMs−1.
Calcium transients in the submembrane shell (black lines) and the compartment core (blue dashed lines) of a two pool model that includes a membrane-bound pump and diffusion into the core. Initial concentration Ca0 is 0.05 μM throughout. Calcium current as in Figure 6.3. Compartment length is 1 μm. (a) Compartment diameter is 1 μm, shell thickness is 0.1 μm; (b) Compartment diameter is 1 μm, shell thickness is 0.01 μm; (c) Compartment diameter is 4 μm, shell thickness is 0.1 μm. Diffusion: DCa = 2.3 × 10−6 cm2 s−1; Pump: Vpump = 10−11 mol cm−2 s−1, Kpump = 10 μM, Jleak = Vpump ∗ Ca0/(Kpump + Ca0).
Calcium transients in (a) the potassium channel colocalised pool, (b) the larger submembrane shell, (c) the compartment core in a three pool model. Note that in (a) the concentration is plotted on a different scale. Compartment 1 μm in diameter with 0.1 μm thick submembrane shell; colocalised membrane occupies 0.001% of the total membrane surface area. Calcium influx into the colocalised pool. Calcium current, diffusion and membrane-bound pump parameters as in Figure 6.5.
Calcium transients in the (a) submembrane shell and (b) cell core (central shell) for different total numbers of shells. Black line: 11 shells. Gray dashed line: 4 shells. Blue dotted line: 2 shells. Diameter is 4 μm and the submembrane shell is 0.1 μm thick. Other shells equally subdivide the remaining compartment radius. All other model parameters are as in Figure 6.5.
Note that the simulation plots correctly show the calcium transients all beginning after the stimulus at 20 msecs, unlike the figure in the book in which part (b) has a spurious time shift! (This is a drawing error, not a simulation error).
Longitudinal diffusion along a 10 μm length of dendrite. Plots show calcium transients in the 0.1 μm thick submembrane shell at different positions along the dendrite. Solid black line: 0.5 μm; dashed: 1.5 μm; dot-dashed: 4.5 μm. (a) Diameter is 1 μm. (b) Diameter is 4 μm. Calcium influx occurs in the first 1 μm length of dendrite only. Each of ten 1 μm long compartment contains four radial shells. Blue dotted line: calcium transient with only radial (and not longitudinal) diffusion in the first 1 μm long compartment. All other model parameters as in Figure 6.5.
Simulation does not reproduce calcium transient without longitudinal diffusion (blue dotted line in figure).
Calcium transients in (a) the 0.1 μm thick submembrane shell and (b) the cell core of a single dendritic compartment of 4 μm diameter with 4 radial shells. Slow buffer with initial concentration 50 μM, forward rate k+ = 1.5 μM-1s−1 and backward rate k− = 0.3 s−1. Blue dotted line: unbuffered calcium transient. Gray dashed line (hidden by solid line): excess (EBA) approximation. Gray dash-dotted line: rapid (RBA) buffer approximation. Binding ratio κ = 250. All other model parameters as in Figure 6.5.
Use Parameters panel in GUI to change parameter values for buffered model, EBA and RBA simultaneously. Same code can generate results for both figures 6.12 and 6.13.
Calcium transients in (a) the 0.1 μm thick submembrane shell and (b) the cell core of a single dendritic compartment of 4 μm diameter with 4 radial shells. Fast buffer with initial concentration 50 μM, forward rate k+ = 500 μM-1s−1 and backward rate k− = 1000 s−1. Black solid line: fixed buffer. Blue dotted line: mobile buffer with diffusion rate Dbuf = 1 × 10−6 cm2 s−1. Gray dashed line: excess (EBA) approximation. Gray dash-dotted line: rapid (RBA) buffer approximation. Binding ratio κ = 25. All other model parameters as in Figure 6.5.
Use Parameters panel to change all parameter values. Code produces results for figures 6.12 and 6.13.