4.4 Article

Direct observation of resonance tryptophan-to-chromophore energy transfer in visible fluorescent proteins

Journal

BIOPHYSICAL CHEMISTRY
Volume 116, Issue 3, Pages 207-212

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.bpc.2005.04.013

Keywords

resonance energy transfer; green fluorescent protein; cyan fluorescent protein; yellow fluorescent protein; tryptophan; time-resolved fluorescence; fluorescence anisotropy

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Visible fluorescent proteins from Aequorea victoria contain next to the fluorophoric group a single tryptophan residue. Both molecules form a single donor-acceptor pair for resonance energy transfer (RET) within the protein. Time-resolved fluorescence experiments using tryptophan excitation have shown that RET is manifested by a distinct growing in of acceptor fluorescence at a rate characteristic for this process. In addition, time-resolved fluorescence anisotropy measurements under the same excitation-emission conditions showed a correlation time that is similar to the time constant of the same RET process with the additional benefit of gaining information on the relative orientation of the corresponding transition dipoles. (c) 2005 Elsevier B.V. All rights reserved.

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