Quast U, Labhardt A M, Doyle V M
Biochem Biophys Res Commun. 1984 Sep 17;123(2):604-11. doi: 10.1016/0006-291x(84)90272-9.
The kinetics of the Quin 2-Ca2+ interaction have been studied using stopped-flow fluorimetry. Mixing the Quin 2-Ca2+ complex with a large excess of EGTA, EDTA or MgCl2 resulted in first order dissociation kinetics. The observed dissociation rate increased slightly with increasing EGTA concentration yielding a limiting value of 83 +/- 4 s-1 for the dissociation rate constant (k-) at pH 7.2, 37 degrees C, +/- 3mM Mg2+. The temperature dependence of the dissociation was weak (activation energy = 22 +/- 1 kJ/mol) and around neutral pH the pH dependence was negligible. The association reaction was too fast to be monitored directly. From this and the instrument dead-time, the second order rate constant k+ was estimated to be greater than or equal to 10(9) M-1s-1, in agreement with the calculation from k+ = k-/K. These data should be useful in evaluating the potential of Quin 2 to measure fast intracellular Ca2+ transients.
已使用停流荧光法研究了喹啉-2(Quin 2)与钙离子(Ca2+)相互作用的动力学。将喹啉-2-钙离子复合物与大量过量的乙二醇双乙醚二胺四乙酸(EGTA)、乙二胺四乙酸(EDTA)或氯化镁(MgCl2)混合,产生一级解离动力学。随着EGTA浓度的增加,观察到的解离速率略有增加,在pH 7.2、37摄氏度、±3毫摩尔镁离子(Mg2+)条件下,解离速率常数(k-)的极限值为83±4秒-1。解离的温度依赖性较弱(活化能=22±1千焦/摩尔),在接近中性pH时,pH依赖性可忽略不计。缔合反应太快,无法直接监测。据此以及仪器死时间,二级速率常数k+估计大于或等于10(9) 摩尔-1秒-1,这与根据k+ = k-/K的计算结果一致。这些数据应有助于评估喹啉-2测量快速细胞内钙离子瞬变的潜力。