Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9890864 | International Journal of Biological Macromolecules | 2005 | 9 Pages |
Abstract
The single Cys residue in the C-terminal domain of bovine eye lens α-crystallin was covalently labelled with 6-bromomethyl-2-(2-furanyl)-3-hydroxychromone. This novel SH-reactive two-band ratiometric fluorescent dye is characterized by excited state intramolecular proton transfer reaction yielding two highly emissive N* and T* bands separated by more than 100 nm. Their relative intensities are known to be highly sensitive to the H-bonding ability of the environment. Properties of the environment of the dye attached to the protein were studied under native-like conditions and at a range of elevated temperatures that are known to facilitate α-crystallin chaperone-like activity. We observe that on heating, the environment of the dye becomes more flexible and the H-bonding of the dye with the protein vicinity decreases. The spectroscopic properties observed on heating were partially restored after cooling, but the initial values were not reached on the time scale of our experiments (up to 3 h). This suggests that the changes of the dye microenvironment are connected with the rearrangements of α-crystallin quaternary structure. Since there is only one Cys residue in αA subunit of α-crystallin (whereas αB subunit contains no Cys), we attributed the observed temperature-induced changes of the dye's microenvironment to the particular site within α-crystallin molecule.
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Authors
Sergiy V. Avilov, Csaba Bode, Ferenc G. Tolgyesi, Andrey S. Klymchenko, Judit Fidy, Alexander P. Demchenko,