Carlier M F, Pantaloni D, Korn E D
J Biol Chem. 1985 Jun 10;260(11):6565-71.
Polymerization under sonication has been developed as a new method to study the rapid polymerization of actin with a large number of elongating sites. The theory proposed assumes that filaments under sonication are maintained at a constant length by the constant input of energy. The data obtained for the reversible polymerization of ADP-actin under sonication have been successfully analyzed according to the proposed model and, therefore, validate the model. The results obtained for the polymerization of ATP-actin under sonication demonstrate the involvement of ATP hydrolysis in the polymerization process. At high actin concentration, polymerization was fast enough, as compared to ATP hydrolysis on the F-actin, to obtain completion of the reversible polymerization of ATP-actin before significant hydrolysis of ATP occurred. A critical concentration of 3 microM was determined as the ratio of the dissociation and association rate constants for the interaction of ATP-actin with the ATP filament ends in 1 mM MgCl2, 0.2 mM ATP. The plot of the rate of elongation of filaments versus actin monomer concentration exhibited an upward deviation at high actin concentration that is consistent with this result. The fact that F-actin at steady state is more stable than the ATP-F-actin polymer at equilibrium suggests that the interaction between ADP-actin and ATP-actin subunits at the end of the ATP-capped filament is much stronger than the interaction between two ATP-actin subunits.
超声作用下的聚合反应已发展成为一种研究肌动蛋白在大量延伸位点处快速聚合的新方法。所提出的理论假设,超声作用下的细丝通过持续的能量输入保持恒定长度。根据所提出的模型,已成功分析了超声作用下ADP - 肌动蛋白可逆聚合反应所获得的数据,因此验证了该模型。超声作用下ATP - 肌动蛋白聚合反应所获得的结果表明ATP水解参与了聚合过程。在高肌动蛋白浓度下,与F - 肌动蛋白上的ATP水解相比,聚合反应足够快,以至于在ATP发生显著水解之前,ATP - 肌动蛋白的可逆聚合反应能够完成。在1 mM MgCl2、0.2 mM ATP条件下,确定3 microM的临界浓度为ATP - 肌动蛋白与ATP细丝末端相互作用的解离和缔合速率常数之比。细丝伸长速率与肌动蛋白单体浓度的关系图在高肌动蛋白浓度下呈现向上偏差,这与该结果一致。稳态下的F - 肌动蛋白比平衡状态下的ATP - F - 肌动蛋白聚合物更稳定,这一事实表明ATP封端细丝末端的ADP - 肌动蛋白与ATP - 肌动蛋白亚基之间的相互作用比两个ATP - 肌动蛋白亚基之间的相互作用要强得多。