Gershman L C, Newman J, Selden L A, Estes J E
Biochemistry. 1984 May 8;23(10):2199-203. doi: 10.1021/bi00305a015.
The delay or lag phase at the onset of polymerization of actin by neutral salt is generally attributed to an actin nucleation reaction. However, when nucleation is circumvented by the use of phalloidin-stabilized nuclei, a lag phase persists when Ca2+-containing actin is polymerized with MgCl2. Pretreatment of actin with ethylene glycol bis(beta-aminoethyl ether)-N,N,N',N'-tetraacetic acid (EGTA) and/or Mg2+ shortens or eliminates this lag phase, suggesting that exchange of the actin-bound divalent cation occurs during this nucleation-independent lag phase. Measurement of the actin-bound cation initially and after brief incubation with EGTA/Mg2+ directly verifies that Mg2+ has replaced Ca2+ as the actin-bound cation, producing a highly polymerizable Mg2+-actin species. Bound-cation exchange prolongs the lag phase in actin polymerization and probably explains what has been termed the monomer activation step in actin polymerization.
中性盐引发肌动蛋白聚合时的延迟或滞后阶段通常归因于肌动蛋白成核反应。然而,当使用鬼笔环肽稳定的核来规避成核时,含Ca2+的肌动蛋白与MgCl2聚合时仍存在滞后阶段。用乙二醇双(β-氨基乙醚)-N,N,N',N'-四乙酸(EGTA)和/或Mg2+预处理肌动蛋白可缩短或消除该滞后阶段,这表明在这个与成核无关的滞后阶段发生了肌动蛋白结合的二价阳离子的交换。对初始时以及与EGTA/Mg2+短暂孵育后的肌动蛋白结合阳离子进行测量,直接证实Mg2+已取代Ca2+成为肌动蛋白结合阳离子,产生了一种高度可聚合的Mg2+ - 肌动蛋白物种。结合阳离子的交换延长了肌动蛋白聚合的滞后阶段,可能解释了肌动蛋白聚合中所谓的单体活化步骤。