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QUENCHING OF TYROSINE FLUORESCENCE BY PHOSPHATE IONS: A MODEL STUDY FOR PROTEIN‐NUCLEIC ACID COMPLEXES
Author(s) -
AlevBehmoaras Tula,
Toulme JeanJacques,
Hélène Claude
Publication year - 1979
Publication title -
photochemistry and photobiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.818
H-Index - 131
eISSN - 1751-1097
pISSN - 0031-8655
DOI - 10.1111/j.1751-1097.1979.tb07177.x
Subject(s) - fluorescence , tyrosine , chemistry , quenching (fluorescence) , deprotonation , nucleic acid , phosphate , photochemistry , ion , biochemistry , organic chemistry , physics , quantum mechanics
— In order to test the ability of phosphate groups to quench the tyrosine fluorescence in nucleic acid‐protein complexes, we have studied the effect of several phosphate ions on the fluorescence of tyrosine derivatives. Mono and bianions (H 2 PO 4 and HPO 4 2– ) which are good proton acceptors quenched the fluorescence of all the phenolic compounds studied except that of O ‐methyl tyrosine. With the other derivatives (tyrosine, N ‐acetyl tyrosinamide and lysyl‐tyrosyl‐α lysine) fluorescence inhibition was accompanied by the appearance of a long wavelength emission (345 nm) attributed to tyrosinate anions. The quenching of tyrosine emission was due to the deprotonation of the phenolic group promoted in the excited state by phosphate ions and leading to the weakly fluorescent tyrosinate ion. Mono and dianions of phosphate mono ester inhibited tyrosine fluorescence as did unesterified phosphates. However, phosphate diester did not have any effect on the fluorescence of tyrosine derivatives. We conclude from this study that in nucleic acid‐protein complexes phosphate groups are not able to quench tyrosine fluorescence except at the end of polynucleotide chains. Since monoester and diester monoanions have a different behavior, we propose that quenching of tyrosine fluorescence by monoanions requires the formation of two hydrogen bonds. This complex cannot form with diesters which consequently do not quench tyrosine fluorescence.