Literature DB >> 9733992

Fluorescence line narrowing applied to the study of proteins.

J Fidy1, M Laberge, A D Kaposi, J M Vanderkooi.   

Abstract

Fluorescence line narrowing is a high resolution spectroscopic technique that uses low temperature and laser excitation to optically select specific subpopulations from the inhomogeneously broadened absorption band of the sample. When applied to the study of fluorescent groups in proteins one can obtain vibronically resolved spectra, which can be analyzed to give information on spectral line shapes, vibrational energies of both the ground and excited state molecule, and the inhomogeneous distribution function of the electronic transitions. These parameters reveal information about the chromophoric prosthetic group and the protein matrix and are functions of geometric strains and local electric fields imposed by the protein. Examples of the use of fluorescence line narrowing are discussed in investigations of heme proteins, photosynthetic systems and tryptophan-containing proteins.

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Year:  1998        PMID: 9733992     DOI: 10.1016/s0167-4838(98)00101-0

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  3 in total

1.  Infrared absorption study of the heme pocket dynamics of carbonmonoxyheme proteins.

Authors:  Andras D Kaposi; Jane M Vanderkooi; Solomon S Stavrov
Journal:  Biophys J       Date:  2006-09-15       Impact factor: 4.033

2.  The enzyme horseradish peroxidase is less compressible at higher pressures.

Authors:  László Smeller; Judit Fidy
Journal:  Biophys J       Date:  2002-01       Impact factor: 4.033

3.  Energy selection is not correlated in the Qx and Qy bands of a Mg-porphyrin embedded in a protein.

Authors:  A Suisalu; K Mauring; J Kikas; L Herenyi; J Fidy
Journal:  Biophys J       Date:  2001-01       Impact factor: 4.033

  3 in total

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