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Principles of Fluorescence Spectroscopy

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PRINCIPLES OF FLUORESCENCE SPECTROSCOPY 227<br />

Figure 6.41. Excimer formation by a self-assembled perylene diimide derivative. Revised and reprinted with permission from [89]. Copyright © 2003,<br />

American Chemical Society. Courtesy <strong>of</strong> Dr. Alex D. Q. Li from the Washington State University.<br />

weakly fluorescent in the absence <strong>of</strong> protein (Figure 6.43).<br />

Addition <strong>of</strong> calmodulin, without calcium, had only a minor<br />

effect on the emission. Addition <strong>of</strong> calcium to calmodulin<br />

resulted in a dramatic increase in the intensity <strong>of</strong> the three<br />

probes. Since the effect was seen with neutral (NPN), negatively<br />

charged (ANS), and partially charged (9-AC)<br />

probes, the binding was interpreted as due to hydrophobic<br />

rather than electrostatic interactions between the probe and<br />

calmodulin.<br />

6.9.3. Binding to Cyclodextrin Using a<br />

Dansyl Probe<br />

While there are numerous examples <strong>of</strong> proteins labeled<br />

with fluorescent probes, relatively few studies are available<br />

using labeled carbohydrates. 98–99 The solvent sensitivity <strong>of</strong><br />

Figure 6.42. Emission spectra <strong>of</strong> acrylodan-labeled fatty acid binding<br />

protein (FABP). The numbers refer to the concentration in µM <strong>of</strong> fatty<br />

acid (oleate) added to 0.2-µM FABP. Revised from [90].

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