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Excited‐state lifetime studies of the three tryptophan residues in the N‐lobe of human serum transferrin
Author(s) -
James Nicholas G.,
Ross Justin A.,
Mason Anne B.,
Jameson David M.
Publication year - 2010
Publication title -
protein science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.353
H-Index - 175
eISSN - 1469-896X
pISSN - 0961-8368
DOI - 10.1002/pro.287
Subject(s) - quantum yield , chemistry , fluorophore , fluorescence , tryptophan , quenching (fluorescence) , excited state , transferrin , analytical chemistry (journal) , emission spectrum , photochemistry , atomic physics , spectral line , biochemistry , chromatography , physics , amino acid , quantum mechanics , astronomy
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.