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Protein Sci. 2010 Jan;19(1):99-110. doi: 10.1002/pro.287.

Excited-state lifetime studies of the three tryptophan residues in the N-lobe of human serum transferrin.

Author information

1
Department of Biochemistry, University of Vermont, College of Medicine, Burlington, Vermont 05405, USA. njames4@hawaii.edu

Abstract

The energy transfer from the three Trp residues at positions 8, 128, and 264 within the human serum transferrin (hTF) N-lobe to the ligand to metal charge transfer band has been investigated by monitoring changes in Trp fluorescence emission and lifetimes. The fluorescence emission from hTF N-lobe is dominated by Trp264, as revealed by an 82% decrease in the quantum yield when this Trp residue is absent. Fluorescence lifetimes were determined by multifrequency phase fluorometry of mutants containing one or two Trp residues. Decays of these samples are best described by two or three discrete lifetimes or by a unimodal Lorentzian distribution. The discrete lifetimes and the center of the lifetime distribution for samples containing Trp128 and Trp264 are affected by iron. The distribution width narrows on iron removal and is consistent with a decrease in dynamic mobility of the dominant fluorophore, Trp264. Both the quantum yield and the lifetimes are lower when iron is present, however, not proportionally. The greater effect of iron on quantum yields is indicative of nonexcited state quenching, i.e., static quenching. The results of these experiments provide quantitative data strongly suggesting that Förster resonance energy transfer is not the sole source of Trp quenching in the N-lobe of hTF.

PMID:
19916167
PMCID:
PMC2817844
DOI:
10.1002/pro.287
[Indexed for MEDLINE]
Free PMC Article

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