Max-Planck-Institute of Biophysics, Kennedy-Allee 70, D-60596, Frankfurt, Germany.
J Fluoresc. 1996 Sep;6(3):159-63. doi: 10.1007/BF00732055.
Stopped-flow kinetic studies have been performed to determine the kinetic parameters of K(+) binding to the fluorescent cryptand F222 and of Na(+)binding to F221 at pH 8.O. The results clearly indicate that a comparatively stable intermediate is formed before the rate-limiting binding step occurs with a rate constant around 30 s(-1) under the chosen experimental conditions. The conversion of the intermediate to the final cation complex is assigned to the final penetration of the already bound, but still partially solvated cation into the ligand's cavity. The main fluorescence intensity change found upon cation binding is attributed to the second reaction step, and not to the fast, initial binding reaction. The comparatively slow overall binding reaction is interpreted on the bases of a special solvate substitution mechanism which, in principle, can also account for the 1500 times slower binding of Ca 2(+) to F221. With regard to time-resolved analytical Na(+) and K(+) determinations, the response times under the chosen conditions are around 20 ms. Differentiation between Na(+) and Ca(2+), for example, is possible with F221 on the basis of completely different response times.
已进行停流动力学研究,以确定在 pH 8.0 下,K(+)与荧光穴醚 F222 结合以及 Na(+)与 F221 结合的动力学参数。结果清楚地表明,在限速结合步骤发生之前,会形成一个相对稳定的中间产物,在所选实验条件下,其速率常数约为 30 s(-1)。将中间产物转化为最终的阳离子配合物归因于已经结合但仍部分溶剂化的阳离子最终进入配体的空腔。阳离子结合时发现的主要荧光强度变化归因于第二反应步骤,而不是快速的初始结合反应。整体结合反应较慢是基于特殊的溶剂取代机制来解释的,原则上,该机制也可以解释 Ca 2(+)与 F221 的结合速度慢 1500 倍。关于时间分辨分析的 Na(+)和 K(+)测定,在所选条件下的响应时间约为 20 ms。例如,基于完全不同的响应时间,可以用 F221 区分 Na(+)和 Ca(2+)。