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1.
J Fluoresc ; 26(1): 355-62, 2016 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-26555288

RESUMO

Live cells contain high concentrations of macromolecules, but almost all experimental biochemical data have been generated from dilute solutions that do not reflect conditions in vivo. To understand biomolecular behavior in vivo, properties studied in vitro are extrapolated to conditions in vivo. Another significant factor which is overlooked is the effects of macromolecular crowding and its consequences in the actual biochemical and physiological environment. Such influences of crowding, its modification and physiological parameters have been reported. The present study investigates the effect of molecular crowding on binding characteristics of Salmon sperm DNA with Bovine hemoglobin and their reconstitutes in presence of molecular crowders viz., Poly ethylene glycol (PEG) and Dextran of different molecular weight by fluorescence, UV visible spectroscopic technique at different temperatures. The results showed that BHb fluorescence was quenched by sDNA through static quenching mechanism which is enhanced in presence of polymers. The number of binding sites 'n' and binding constants 'K' were determined at different temperatures based on fluorescence quenching. The thermodynamic parameters namely ∆H°, ∆G°, T∆S° were studied at different temperatures and the results indicate that hydrophobic forces are predominant in the sDNA-BHb complex. Negative ∆G° values imply that the binding process is spontaneous.


Assuntos
DNA/química , Dextranos/química , Hemoglobinas/química , Polietilenoglicóis/química , Termodinâmica , Animais , Bovinos , Substâncias Macromoleculares/química , Masculino , Salmão , Espectrometria de Fluorescência , Espectrofotometria Ultravioleta , Espermatozoides
2.
J Fluoresc ; 24(4): 1275-84, 2014 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-24894381

RESUMO

Biological macromolecules evolve and function within intracellular environments that are crowded with other macromolecules. Crowding results in surprisingly large quantitative effects on both the rates and the equilibria of interactions involving macromolecules, but such interactions are commonly studied outside the cell in uncrowded buffers. The addition of high concentrations of natural and synthetic macromolecules to such buffers enables crowding to be mimicked in vitro, and should be encouraged as a routine variable to study. In this study, we propose to understand the changes in DNA character and its modulation in presence of macromolecules such as PEG with reference to binding parameters to amino acids using fluorescence enhancement.


Assuntos
Aminoácidos/química , DNA/química , Aminoácidos/análise , DNA/análise , Fluorescência , Substâncias Macromoleculares/análise , Substâncias Macromoleculares/química , Polietilenoglicóis/química , Espectrometria de Fluorescência , Termodinâmica
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