Frieden C
Proc Natl Acad Sci U S A. 1983 Nov;80(21):6513-7. doi: 10.1073/pnas.80.21.6513.
A detailed mechanism that fully accounts for the Mg2+-induced polymerization of actin in the presence or absence of Ca2+ at 20 degrees C and pH 8 is presented. In the absence of Ca2+, the mechanism of the Mg2+-induced polymerization is as follows: Mg2+ binds to a metal-binding site on G-actin and induces a conformational change, which is required for eventual polymerization. The overall dissociation constant for this binding is about 30 microM. This actin species then binds a second molecule of Mg2+ (Kd = 5 mM), which yields a species capable of polymerization. Dimer formation from this monomeric species is quite unfavorable, but trimer formation from dimer and monomer is much more favorable. The trimer may then elongate to give filaments. Ca2+, when present, binds at the same site as the tightly bound Mg2+ and must be displaced by Mg2+ before the conformational change can occur. The rate and dissociation constants for tight binding of Ca2+ and Mg2+ and for the conformational change are consistent with those observed previously by using a fluorescently labeled G-actin. With the mechanism proposed, it is possible to fit the full time course of polymerization over a wide range of actin concentrations, Mg2+ concentrations, and Ca2+ concentrations.
本文提出了一种详细机制,该机制能够充分解释在20摄氏度、pH值为8的条件下,无论有无Ca2+存在时,Mg2+诱导肌动蛋白聚合的过程。在无Ca2+时,Mg2+诱导聚合的机制如下:Mg2+与G-肌动蛋白上的一个金属结合位点结合并诱导构象变化,这是最终聚合所必需的。这种结合的总解离常数约为30 microM。然后这种肌动蛋白物种结合第二个Mg2+分子(Kd = 5 mM),从而产生一种能够聚合的物种。从这种单体物种形成二聚体非常不利,但从二聚体和单体形成三聚体则更为有利。三聚体随后可能伸长形成细丝。当存在Ca2+时,它与紧密结合的Mg2+结合在同一位置,并且在构象变化发生之前必须被Mg2+取代。Ca2+和Mg2+紧密结合以及构象变化的速率和解离常数与先前使用荧光标记的G-肌动蛋白观察到的结果一致。基于所提出的机制,有可能拟合在广泛的肌动蛋白浓度、Mg2+浓度和Ca2+浓度范围内聚合的完整时间进程。