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A flow-dialysis method for obtaining relative measures of association constants in calmodulin-metal-ion systems.

机译:一种用于获得钙调蛋白-金属离子系统中缔合常数的相对量度的流透析方法。

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摘要

A flow-dialysis apparatus suitable for the study of high-affinity metal-binding proteins has been utilized to study calmodulin-metal exchange as a measure of relative calmodulin-metal association constants. Calmodulin labelled with radioactive 153Gd was dialysed against buffer containing various competing metal ions. The rate of label exchange was monitored by a gamma-ray scintillation detector. Competing metals used were Ca2+ and Cd2+, and the lanthanides Gd3+, Eu3+, La3+ and Lu3+. All exchange processes were first-order, and two categories of metal were found: Ca2+ and Cd2+ in one, the lanthanides comprising the other. In addition calmodulin-metal complexes with radioactive 109Cd and 45Ca released the bound label without any competing metal being added to the buffer. The kinetics of this metal loss can be described by two consecutive first-order processes, and the fraction of label associated with each rate can be determined. Studies of phosphodiesterase activation by calmodulin show Cd2+ and calmodulin to cause 80% of the maximum activation found when Ca2+ and calmodulin are used.
机译:适于研究高亲和力金属结合蛋白的流式透析仪已被用于研究钙调蛋白与金属的交换,以此作为相对钙调蛋白与金属缔合常数的量度。用含各种竞争性金属离子的缓冲液透析标记有放射性153Gd的钙调蛋白。通过γ射线闪烁检测器监测标记交换的速率。使用的竞争金属是Ca2 +和Cd2 +,以及镧系元素Gd3 +,Eu3 +,La3 +和Lu3 +。所有交换过程都是一阶的,并且发现了两类金属:一种是Ca2 +和Cd2 +,另一种是镧系元素。另外,具有放射性109Cd和45Ca的钙调蛋白-金属络合物释放了结合的标记,而没有任何竞争性金属添加到缓冲液中。这种金属损失的动力学可以通过两个连续的一阶过程来描述,并且可以确定与每种速率相关的标记分数。钙调蛋白激活磷酸二酯酶的研究表明,当使用Ca2 +和钙调蛋白时,Cd2 +和钙调蛋白引起最大激活的80%。

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