Tellinghuisen Joel
Department of Chemistry, Vanderbilt University, Nashville, TN 37235, U.S.A.
Anal Biochem. 2008 Feb 15;373(2):395-7. doi: 10.1016/j.ab.2007.08.039. Epub 2007 Sep 2.
In the study of 1:1 binding, M + X right arrow over left arrow MX, isothermal titration calorimetry (ITC) can be used successfully at values of c=KM well below the value 1.0 that is often considered its lower limit. However, analysis of low-c ITC data may require freezing the stoichiometry parameter n, and that is thought to be prohibitive for biological systems, where n can be poorly known. Here it is noted that the least-squares estimates of the binding constant K are virtually independent of errors in n at low c, permitting reliable determination of K and, from its temperature dependence, DeltaH degrees and n, down to c=10(-4) or lower, ligand solubility permitting.
在1:1结合反应M + X ⇌ MX的研究中,对于c = KM远低于通常认为的下限值1.0的情况,等温滴定量热法(ITC)能够成功应用。然而,对低c值的ITC数据进行分析可能需要固定化学计量参数n,而这对于生物系统而言被认为是不可行的,因为在生物系统中n可能难以准确知晓。在此需指出的是,在低c值时,结合常数K的最小二乘估计实际上与n的误差无关,从而能够可靠地确定K,并根据其对温度的依赖性确定ΔH°和n,直至c = 10⁻⁴或更低,前提是配体具有足够的溶解度。