Wang T
J Biol Chem. 1986 May 15;261(14):6307-19.
We have observed two modes each of ADP and K+ regulation of phosphoenzyme (EP) intermediates formed in the early phase of skeletal sarcoplasmic reticulum hydrolysis of ATP at 20 degrees C, using, for the first time, a five-syringe quench flow apparatus for transient-state kinetic measurements. The total acid-stable EP formed for 20.5 and 116 ms in the K+ medium appears to be composed of either two monomers in rapid equilibrium, E1P in equilibrium E'1P, or a dimer of the two subunits, PE1E'1P. The ADP-sensitive E1P may form an acid-labile ADP X E1P (or ATP X E1) complex rapidly, giving ATP as a consequence of acid quenching. The ADP may also induce decomposition of the ADP-reactive E'1P. Monomeric and dimeric mechanisms are introduced to account for the hyperbolic relation between the rate constant of the ADP-induced E'1P decomposition and [ADP], consistent with the fact that the E'1P may also give ATP in the presence of ADP. As to the K+ effects, the K+, which is bound to the unphosphorylated enzyme and possibly becomes occluded during EP formation, may either facilitate the one-to-one E1P in equilibrium E'1P equilibrium or maintain the dimeric functional unit. The subsequent forward transformation of the E'1P to the ADP-insensitive K+-sensitive E'2P, possibly the rate-determining step for the catalytic cycle, is found to be K+ independent. The major effect of the K+ in the medium is its catalytic cleavage of the E'2P, which is detected as the missing EP under these conditions. When K+ is not involved in the EP formation, the forward sequential transformation E1P----E'1P----E'2P----E2P or PE1E'1P----PE'2E2P is apparent in the time range from 20.5 to 116 ms after EP formation, and the E'2P may accumulate in the K+ devoid medium and be detected as the major component of the total acid-stable EP. The Mg2+-sensitive E2P represents the EP missing in the medium containing no ADP and K+.
我们首次使用五注射器淬灭流动装置进行瞬态动力学测量,观察到了在20℃下骨骼肌肌浆网ATP水解早期形成的磷酸酶(EP)中间体的ADP和K⁺调节的两种模式。在K⁺介质中20.5毫秒和116毫秒形成的总酸稳定EP似乎由处于快速平衡的两种单体(E1P处于平衡态E'1P)或两个亚基的二聚体(PE1E'1P)组成。ADP敏感的E1P可能迅速形成酸不稳定的ADP X E1P(或ATP X E1)复合物,酸淬灭后产生ATP。ADP也可能诱导ADP反应性E'1P的分解。引入单体和二聚体机制来解释ADP诱导的E'1P分解速率常数与[ADP]之间的双曲线关系,这与E'1P在ADP存在下也能产生ATP的事实一致。至于K⁺的作用,与未磷酸化酶结合且可能在EP形成过程中被封闭的K⁺,可能促进E1P与E'1P的一对一平衡,或维持二聚体功能单元。随后E'1P向对ADP不敏感、对K⁺敏感的E'2P的正向转化,可能是催化循环的速率决定步骤,发现其与K⁺无关。介质中K⁺的主要作用是催化E'2P的裂解,在这些条件下检测为缺失的EP。当K⁺不参与EP形成时,在EP形成后20.5至116毫秒的时间范围内,E1P→E'1P→E'2P→E2P或PE1E'1P→PE'2E2P的正向顺序转化很明显,并且E'2P可能在不含K⁺的介质中积累,并被检测为总酸稳定EP的主要成分。Mg²⁺敏感的E2P代表不含ADP和K⁺的介质中缺失的EP。