The non-natural amino acid p-cyanophenylalanine (Phe(CN)) has recently emerged as a useful fluorescent probe of proteins; however, its photophysical properties have not been systematically examined. Herein, we measure the fluorescence quantum yield and the fluorescence lifetime of Phe(CN) in a series of solvents. It is found that the fluorescence lifetime of Phe(CN) shows a linear dependence on the Kamlet-Taft parameter α of the protic solvents used, indicating that the solute-solvent hydrogen bonding interactions mediate the non-radiative decay rate. Thus, results of this study provide a basis for quantitative application of Phe(CN) fluorescence in protein conformational studies.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2857417 | PMC |
http://dx.doi.org/10.1016/j.cplett.2010.01.058 | DOI Listing |
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