Alteration of tryptophan fluorescence properties upon dissociation of Lumbricus terrestris hemoglobin

Rhoda Elison Hirsch, Gediminas J A Vidugiris, Joel M. Friedman, John P. Harrington

Research output: Contribution to journalArticle

10 Citations (Scopus)

Abstract

Fluorescence analysis has been used to study dissociation of the dodecameric 3.8 kDa Lumbricus terrestris hemoglobin. Since tryptophan intrinsic fluorescence has been used as a reporter group to study Lumbricus hemoglobin, it is of interest to study dissociation perturbed properties of the tryptophan residues. Shifts in the fluorescence emission maximum to longer wavelengths upon dissociation at pH 9.2 suggest that tryptophans buried at the subunit interface(s) become more exposed. Fluorescence lifetime and quenching studies are employed in this present investigation as a means to confirm the location of tryptophan residues at the subunit interfaces. Acrylamide titration (to 2.5 M) indicate only a fraction of the residues can be quenched at either pH. At pH 7.0, the Stern-Volmer plot has downward curvature, while at pH 9.2 there is slight upward curvature, again indicating a change in environment. The intrinsic fluorescence decay requires at least four exponentials at both pHs. The mean fluorescence lifetime of CO Lumbricus hemoglobin increases from 1.1 ns at pH 7 to 3.3 ns at pH 9.2. The lifetime data can be further interpreted as a decrease in the quenching of residues with a ≈ 30 ps lifetime, and a concomitant increase in the longer lifetime components. This is consistent with interface tryptophans becoming exposed to solvent upon dissociation, and loss of quenching by intersubunit hemes. The overall results suggest that in the dodecamer, most of the tryptophans are located in a hydrophobic environment, not all of which are located at the subunit interface.

Original languageEnglish (US)
Pages (from-to)248-251
Number of pages4
JournalBiochimica et Biophysica Acta (BBA)/Protein Structure and Molecular
Volume1205
Issue number2
DOIs
StatePublished - Apr 13 1994

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Oligochaeta
Tryptophan
Hemoglobins
Fluorescence
Quenching
Acrylamide
Carbon Monoxide
Heme
Titration
Wavelength

Keywords

  • (L. terrestris)
  • Dissociation
  • Fluorescence lifetime
  • Fluorescence quenching
  • Hemoglobin

ASJC Scopus subject areas

  • Biochemistry
  • Biophysics
  • Molecular Biology
  • Structural Biology

Cite this

Alteration of tryptophan fluorescence properties upon dissociation of Lumbricus terrestris hemoglobin. / Hirsch, Rhoda Elison; Vidugiris, Gediminas J A; Friedman, Joel M.; Harrington, John P.

In: Biochimica et Biophysica Acta (BBA)/Protein Structure and Molecular, Vol. 1205, No. 2, 13.04.1994, p. 248-251.

Research output: Contribution to journalArticle

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