ABSTRACT
The present study deals with the photophysical properties of triguanosine diphosphate in aqueous solutions, which are compared with those of the 2'-deoxyguanosine monophosphate. They are studied by steady-state absorption and fluorescence spectroscopy as well as by time-resolved fluorescence spectroscopy with femtosecond resolution. The temperature, salt and concentration dependence of the absorption and fluorescence spectra reveal that association of the trimers takes place. The resulting aggregates could correspond to a tetraplex structure. The aggregate fluorescence quantum yield is higher and the fluorescence lifetime much longer than those of the monomer. These results show the interaction between guanosine residues that may manifest itself via self-solvation, hydrogen bonding and/or delocalization of the excitation.
Subject(s)
Guanosine Diphosphate/chemistry , Guanosine Diphosphate/radiation effects , Light , Deoxyguanine Nucleotides/chemistry , Deoxyguanine Nucleotides/radiation effects , Fluorescence , Guanosine Diphosphate/analogs & derivatives , Hydrogen Bonding , Molecular Structure , Photochemistry , Spectrometry, Fluorescence , Temperature , Water/chemistryABSTRACT
Cytosine methylation, which determines the hot spots for DNA photo-damage, is shown to induce a red-shift of the nucleoside absorption spectrum, making the chromophore more vulnerable to solar radiation, and a tenfold increase of the fluorescence lifetime, making excited statereactions more probable. A femtosecond investigation of the excited state deactivation reveals a quite complex mechanism.
Subject(s)
Cytidine/analogs & derivatives , Cytidine/chemistry , Spectrometry, Fluorescence , Spectrophotometry, UltravioletABSTRACT
A series of biochip readers developed for gel-based biochips includes three imaging models and a novel nonimaging biochip scanner. The imaging readers, ranging from a research-grade versatile reader to a simple portable one, use wide-field objectives and 12-bit digital large-coupled device cameras for parallel addressing of multiple array elements. This feature is valuable for monitoring the kinetics of sample interaction with immobilized probes. Depending on the model and the label used, the sensitivity of these readers approaches 0.3 amol of a labeled sample per gel element. In the selective scanner, both the spot size of the excitation laser beam and the detector field of view match the size of the biochip array elements so that the whole row of the array can be read in a single scan. The portable version reads 50-mm long, 150-element, one-dimensional arrays in 5 s. With a dynamic range of 4000:1, a sensitivity of 1-5 amol of a labeled sample per gel element, and a data format facilitating online processing, the scanner is an attractive, inexpensive solution for biomedical diagnostics. Fluorophores for sample labeling were compared experimentally in terms of detection sensitivity, influence on duplex stability, and suitability for multilabel analysis and thermodynamic studies. Texas Red and tetracarboxyphenylporphyn proved to be the best choice for two-wavelength analysis using the imaging readers.
