Skip to main content
Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1978 Oct;75(10):4652–4656. doi: 10.1073/pnas.75.10.4652

Nonexponential fluorescence decay of aqueous tryptophan and two related peptides by picosecond spectroscopy

G R Fleming †,, J M Morris , R J Robbins †,, G J Woolfe , P J Thistlethwaite , G W Robinson §
PMCID: PMC336174  PMID: 16592569

Abstract

Time-resolved fluorescence spectroscopy of tryptophan and two related dipeptides, tryptophylalanine and alanyltryptophan, has been carried out on the subnanosecond time scale by using picosecond exciting pulses at a wavelength of 264 nm. Detection was with an ultrafast streak camera coupled to an optical multichannel analyzer. The zwitterions of these molecules show a definite nonexponential fluorescence decay which can be analyzed in terms of two exponentials. The two decay rates increase strongly with increasing temperature, as does the weight of the faster component. In tryptophan at pH 11, where the amino group is deprotonated, there remains only a single temperature-dependent exponential. The results are interpreted in terms of two kinds of trapped conformers in the excited state that interconvert no quicker than the time scale of the fluorescence. A model is suggested in which the nonradiative processes in one conformer approximate those in the bare indole moiety. The nonradiative decay rate of the other conformer is substantially faster. It is believed that the process responsible for this fast decay is intramolecular electron transfer from the indole to the amino acid side chain. The predilection for this electron transfer depends on steric relationships as well as on the electron-attracting power of the carbonyl group. This picture is consistent with earlier fluorescence quantum yield results. In fact, a self-consistent picture emerges from the temporal and yield data that quantitatively explains most important facets of tryptophan photochemistry in aqueous solution.

Keywords: protein fluorescence, photoionization, electron transfer, ultrafast primary processes

Full text

PDF
4652

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Bent D. V., Hayon E. Excited state chemistry of aromatic amino acids and related peptides. III. Tryptophan. J Am Chem Soc. 1975 May 14;97(10):2612–2619. doi: 10.1021/ja00843a004. [DOI] [PubMed] [Google Scholar]
  2. COWGILL R. W. Fluorescence and the structure of proteins. I. Effects of substituents on the fluorescence of indole and phenol compounds. Arch Biochem Biophys. 1963 Jan;100:36–44. doi: 10.1016/0003-9861(63)90031-6. [DOI] [PubMed] [Google Scholar]
  3. De Lauder W. B., Wahl P. pH dependence of the fluorescence decay of tryptophan. Biochemistry. 1970 Jun 23;9(13):2750–2754. doi: 10.1021/bi00815a025. [DOI] [PubMed] [Google Scholar]
  4. Eisinger J. A variable temperature, U.V. luminescence spectrograph for small samples. Photochem Photobiol. 1969 Mar;9(3):247–258. doi: 10.1111/j.1751-1097.1969.tb07289.x. [DOI] [PubMed] [Google Scholar]
  5. Eisinger J., Navon G. Fluorescence quenching and isotope effect of tryptophan. J Chem Phys. 1969 Mar 1;50(5):2069–2077. doi: 10.1063/1.1671335. [DOI] [PubMed] [Google Scholar]
  6. Grossweiner L. I., Kaluskar A. G., Baugher J. F. Flash photolysis of enzymes. Int J Radiat Biol Relat Stud Phys Chem Med. 1976 Jan;29(1):1–16. doi: 10.1080/09553007614551511. [DOI] [PubMed] [Google Scholar]
  7. Steiner R. F., Kirby E. P. The interaction of the ground and excited states of indole derivatives with electron scavengers. J Phys Chem. 1969 Dec;73(12):4130–4135. doi: 10.1021/j100846a015. [DOI] [PubMed] [Google Scholar]
  8. Strickland E. H., Horwitz J., Billups C. Near-ultraviolet absorption bands of tryptophan. Studies using indole and 3-methylindole as models. Biochemistry. 1970 Dec 8;9(25):4914–4921. doi: 10.1021/bi00827a013. [DOI] [PubMed] [Google Scholar]
  9. Tatischeff I., Klein R. Influence of the environment on the excitation wavelength dependence of the fluorescence quantum yield of indole. Photochem Photobiol. 1975 Dec;22(6):221–229. doi: 10.1111/j.1751-1097.1975.tb06740.x. [DOI] [PubMed] [Google Scholar]
  10. Templer H., Thistlethwaite P. J. Flash photolysis of aqueous tryptophan, alanyl tryptophan and tryptophyl alanine. Photochem Photobiol. 1976 Feb;23(2):79–83. doi: 10.1111/j.1751-1097.1976.tb06777.x. [DOI] [PubMed] [Google Scholar]
  11. Valeur B., Weber G. Resolution of the fluorescence excitation spectrum of indole into the 1La and 1Lb excitation bands. Photochem Photobiol. 1977 May;25(5):441–444. doi: 10.1111/j.1751-1097.1977.tb09168.x. [DOI] [PubMed] [Google Scholar]

Articles from Proceedings of the National Academy of Sciences of the United States of America are provided here courtesy of National Academy of Sciences

RESOURCES