Tajc Stephen G, Tolbert Blanton S, Basavappa Ravi, Miller Benjamin L
Department of Biochemistry and Biophysics, University of Rochester, Rochester, New York 14642, USA.
J Am Chem Soc. 2004 Sep 1;126(34):10508-9. doi: 10.1021/ja047929u.
Knowledge of the acid dissociation constant (pKa) of a molecule is a critical step toward understanding its structure and reactivity. Current methods for pKa measurement, including electrochemical, spectroscopic, and spectrophotometric titrations, have proven to be useful but also have significant limitations. To overcome these limitations, we report the use of isothermal titration calorimetry (ITC) as a new method for pKa determination. We demonstrate by the measurement of the pKa values for free cysteine, glutathione, and a cysteine residue in a protein that this method is rapid and accurate.
了解分子的酸解离常数(pKa)是理解其结构和反应活性的关键一步。目前用于测量pKa的方法,包括电化学、光谱和分光光度滴定法,已被证明是有用的,但也有显著的局限性。为了克服这些局限性,我们报告了使用等温滴定量热法(ITC)作为一种测定pKa的新方法。我们通过测量游离半胱氨酸、谷胱甘肽和蛋白质中半胱氨酸残基的pKa值证明,该方法快速且准确。