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Figure 1.
Fig. 1. Time course of fluorescence at 416 nm after jumping
from the peptide stock solution in TFE/LiCl into the final
buffer solution using 20 μM Abz-Ala-Ala-Pro-Phe-NH-Np at 10°C.
A, uncatalyzed (k=7.9×10^3 s^−1); B, 1 nM rhCyp18cy
(k=15.3×10^3 s^−1). Measurements were done in 35 mM
HEPES pH 7.8, λ[ex]=320 nm.
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