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Photophysical Properties of BADAN Revealed in the Study of GGBP Structural Transitions.
- Source :
-
International journal of molecular sciences [Int J Mol Sci] 2021 Oct 15; Vol. 22 (20). Date of Electronic Publication: 2021 Oct 15. - Publication Year :
- 2021
-
Abstract
- The fluorescent dye BADAN (6-bromoacetyl-2-dimetylaminonaphtalene) is widely used in various fields of life sciences, however, the photophysical properties of BADAN are not fully understood. The study of the spectral properties of BADAN attached to a number of mutant forms of GGBP, as well as changes in its spectral characteristics during structural changes in proteins, allowed to shed light on the photophysical properties of BADAN. It was shown that spectral properties of BADAN are determined by at least one non-fluorescent and two fluorescent isomers with overlapping absorbing bands. It was found that BADAN fluorescence is determined by the unsolvated "PICT" (planar intramolecular charge transfer state) and solvated "TICT" (twisted intramolecular charge transfer state) excited states. While "TICT" state can be formed both as a result of the "PICT" state solvation and as a result of light absorption by the solvated ground state of the dye. BADAN fluorescence linked to GGBP/H152C apoform is quenched by Trp 183, but this effect is inhibited by glucose intercalation. New details of the changes in the spectral characteristics of BADAN during the unfolding of the protein apo and holoforms have been obtained.
- Subjects :
- 2-Naphthylamine chemistry
2-Naphthylamine pharmacology
Amino Acid Substitution
Escherichia coli
Escherichia coli Proteins drug effects
Escherichia coli Proteins genetics
Escherichia coli Proteins metabolism
Fluorescence
Fluorescent Dyes chemistry
Fluorescent Dyes pharmacology
Monosaccharide Transport Proteins drug effects
Monosaccharide Transport Proteins genetics
Monosaccharide Transport Proteins metabolism
Mutation, Missense
Protein Conformation drug effects
Spectrometry, Fluorescence methods
Structure-Activity Relationship
2-Naphthylamine analogs & derivatives
Escherichia coli Proteins chemistry
Monosaccharide Transport Proteins chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 1422-0067
- Volume :
- 22
- Issue :
- 20
- Database :
- MEDLINE
- Journal :
- International journal of molecular sciences
- Publication Type :
- Academic Journal
- Accession number :
- 34681772
- Full Text :
- https://doi.org/10.3390/ijms222011113