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. 2008 Sep 12;95(11):5399–5411. doi: 10.1529/biophysj.107.114587

FIGURE 2.

FIGURE 2

Normalized experimental (dotted line) and fitted (solid line) fluorescence rise and decay curves of the Venus acceptor, detected at 557 nm, in YC3.60 on donor excitation at 400 nm. In A the data are presented with a time scale of 5 ps/channel, whereas this is 1 ps/channel in B, in which only the first nanosecond is shown. Curve 1 is the fluorescence intensity trace of YC3.60 in the absence of Ca2+, whereas curve 2 is that of YC3.60 in the presence of Ca2+. Curve 3 represents the reference compound xanthione in ethanol. In B it can be observed that the rise time of curve 2 is shorter than that of curve 1, because curve 2 is already starting to decay. The experimental data taken at both time scales are globally analyzed using a bi-exponential rise (in case of calcium-free YC3.60) and mono-exponential decay model with amplitudes αi and lifetimes τi as adjustable parameters for obtaining an optimal fit. The recovered parameters (α, τ) are collected in Table 1 (case 3). Weighted residuals are presented in the bottom panels. Global χ2 values are, respectively, for YC3.60 in absence of Ca2+ 1.05, and for YC3.60 in presence of Ca2+ 1.05.