Article ID Journal Published Year Pages File Type
10532751 Analytical Biochemistry 2012 10 Pages PDF
Abstract
Literature recommendations for designing isothermal titration calorimetry (ITC) experiments to study 1:1 binding, M + X ⇄ MX, are not consistent and have persisted through time with little quantitative justification. In particular, the “standard protocol” employed by most workers involves 20 to 30 injections of titrant to a final titrant/titrand mole ratio (Rm) of ∼ 2-a scheme that can be far from optimal and can needlessly limit applicability of the ITC technique. These deficiencies are discussed here along with other misconceptions. Whether a specific binding process can be studied by ITC is determined less by c (the product of binding constant K and titrand concentration [M]0) than by the total detectable heat qtot and the extent to which M can be converted to MX. As guidelines, with 90% conversion to MX, K can be estimated within 5% over the range 10 to 108 M−1 when qtot/σq ≈ 700, where σq is the standard deviation for estimation of q. This ratio drops to ∼ 150 when the stoichiometry parameter n is treated as known. A computer application for modeling 1:1 binding yields realistic estimates of parameter standard errors for use in protocol design and feasibility assessment.
Related Topics
Physical Sciences and Engineering Chemistry Analytical Chemistry
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