kinITC: a new method for obtaining joint thermodynamic and kinetic data by isothermal titration calorimetry.
Fiche publication
Date publication
janvier 2012
Journal
Journal of the American Chemical Society
Auteurs
Membres identifiés du Cancéropôle Est :
Dr ENNIFAR Eric
Tous les auteurs :
Burnouf D, Ennifar E, Guedich S, Puffer B, Hoffmann G, Bec G, Disdier F, Baltzinger M, Dumas P
Lien Pubmed
Résumé
Isothermal titration calorimetry (ITC) is the method of choice for obtaining thermodynamic data on a great variety of systems. Here we show that modern ITC apparatus and new processing methods allow researchers to obtain a complete kinetic description of systems more diverse than previously thought, ranging from simple ligand binding to complex RNA folding. We illustrate these new features with a simple case (HIV-1 reverse transcriptase/inhibitor interaction) and with the more complex case of the folding of a riboswitch triggered by the binding of its ligand. The originality of the new kinITC method lies in its ability to dissect, both thermodynamically and kinetically, the two components: primary ligand binding and subsequent RNA folding. We are not aware of another single method that can yield, in a simple way, such deep insight into a composite process. Our study also rationalizes common observations from daily ITC use.
Mots clés
Calorimetry, methods, HIV Reverse Transcriptase, antagonists & inhibitors, HIV-1, enzymology, Kinetics, Nevirapine, metabolism, Reverse Transcriptase Inhibitors, metabolism, Riboswitch, Statistics as Topic, methods, Thermodynamics, Thiamine Pyrophosphate, metabolism
Référence
J. Am. Chem. Soc.. 2012 Jan 11;134(1):559-65