| Literature DB >> 26794354 |
Philippe Dumas1, Eric Ennifar2, Cyrielle Da Veiga2, Guillaume Bec2, William Palau3, Carmelo Di Primo3, Angel Piñeiro4, Juan Sabin5, Eva Muñoz5, Javier Rial5.
Abstract
Isothermal titration calorimetry (ITC) has long been used for kinetic studies in chemistry, but this remained confined to enzymatic studies in the biological field. In fact, the biological community has long had the tendency of ignoring the kinetic possibilities of ITC considering it solely as a thermodynamic technique, whereas surface plasmon resonance is seen as the kinetic technique par excellence. However, the primary signal recorded by ITC is a heat power which is directly related to the kinetics of the reaction. Here, it is shown how this kinetic signal can be recovered by using kinITC, the kinetic extension of ITC. The theoretical basis of kinITC is detailed for the most common situation of a second-order reaction A+B Ω C characterized by kinetic parameters kon, koff. A simplified kinITC-ETC method based upon the determination of an "Equilibration Time Curve" (ETC) is presented. The ETC is obtained by automatic determination of the "effective end" of each injection. The method is illustrated with experimental results with a comparison to Surface Plasmon Resonance (SPR) data. kon values were obtained in a wide range, from 10(3) to 0.5×10(6) M(-1) s(-1). All procedures were implemented in the program AFFINImeter (https://www.affinimeter.com/).Keywords: Biological calorimetry; Equilibration time curve; ITC; Kinetics; Microcalorimetry; kinITC
Mesh:
Year: 2015 PMID: 26794354 DOI: 10.1016/bs.mie.2015.08.026
Source DB: PubMed Journal: Methods Enzymol ISSN: 0076-6879 Impact factor: 1.600