Kennedy B G, Lunn G, Hoffman J F
J Gen Physiol. 1986 Jan;87(1):47-72. doi: 10.1085/jgp.87.1.47.
Resealed human red blood cell ghosts were prepared to contain a range of ADP concentrations at fixed ATP concentrations and vice versa. ATP/ADP ratios ranging from approximately 0.2 to 50 were set and maintained (for up to 45 min) in this system. ATP and ADP concentrations were controlled by the addition of either a phosphoarginine- or phosphocreatine-based regenerating system. Ouabain-sensitive unidirectional Na efflux was determined in the presence and absence of 15 mM external K as a function of the nucleotide composition. Na/K exchange was found to increase to saturation with ATP (K 1/2 approximately equal to 250 microM), whereas Na/Na exchange (measured in K-free solutions) was a saturating function of ADP (K 1/2 approximately equal to 350 microM). The elevation of ATP from approximately 100 to 1,800 microM did not appreciably affect Na/Na exchange. In the presence of external Na and a saturating concentration of external K, increasing the ADP concentration at constant ATP was found to decrease ouabain-sensitive Na/K exchange. The decreased Na/K exchange that still remained when the ADP/ATP ratio was high was stimulated by removal of external Na. Assuming that under normal substrate conditions the reaction cycle of the Na/K pump is rate-limited by the conformational change associated with the release of occluded K [E2 X (K) X ATP----E1 X ATP + K], increasing ADP inhibits the rate of these transformations by competition with ATP for the E2(K) form. A less likely alternative is that inhibition is due to competition with ATP at the high-affinity site (E1). The acceleration of the Na/K pump that occurs upon removing external Na at high levels of ADP evidently results from a shift in the forward direction of the transformation of the intermediates involved with the release of occluded Na from E1P X (Na). Thus, the nucleotide composition and the Na gradient can modulate the rate at which the Na/K pump operates.
制备重新封闭的人红细胞血影,使其在固定的ATP浓度下含有一系列ADP浓度,反之亦然。在该系统中设定并维持(长达45分钟)约0.2至50的ATP/ADP比率。通过添加基于磷酸精氨酸或磷酸肌酸的再生系统来控制ATP和ADP的浓度。在有和没有15 mM外部K的情况下,测定哇巴因敏感的单向Na外流作为核苷酸组成的函数。发现Na/K交换随ATP增加至饱和(K 1/2约等于250 microM),而Na/Na交换(在无K溶液中测量)是ADP的饱和函数(K 1/2约等于350 microM)。ATP从约100 microM升高至1800 microM对Na/Na交换没有明显影响。在存在外部Na和饱和浓度的外部K的情况下,发现在恒定ATP下增加ADP浓度会降低哇巴因敏感的Na/K交换。当ADP/ATP比率高时仍然存在的Na/K交换减少受到去除外部Na的刺激。假设在正常底物条件下,Na/K泵的反应循环受与封闭K释放相关的构象变化的速率限制[E2 X (K) X ATP----E1 X ATP + K],增加ADP通过与ATP竞争E2(K)形式来抑制这些转化的速率。另一种可能性较小的是,抑制是由于在高亲和力位点(E1)与ATP竞争。在高ADP水平下去除外部Na时发生的Na/K泵加速显然是由于与从E1P X (Na)释放封闭Na相关的中间体转化向前方向的转变。因此,核苷酸组成和Na梯度可以调节Na/K泵的运行速率。