Asturias F J, Blasie J K
Department of Chemistry, University of Pennsylvania, Philadelphia 19104.
Biophys J. 1989 Apr;55(4):739-53. doi: 10.1016/S0006-3495(89)82873-5.
Direct measurements of phosphorylation of the Ca2+ ATPase of the sarcoplasmic reticulum (SR) have shown that the lifetime of the first phosphorylated intermediate in the Ca2+ transport cycle, E1 approximately P, increases with decreasing [Mg2+] (Dupont, Y. 1980. Eur. J. Biochem. 109:231-238). Previous x-ray diffraction work (Pascolini, D., and J.K. Blasie. 1988. Biophys. J. 54:669-678) under high [Mg2+] conditions (25 mM) indicated that changes in the profile structure of the SR membrane could be responsible for the low-temperature transient trapping of E1 approximately P that occurs at temperatures below 2-3 degrees C, the upper characteristic temperature th for lipid lateral phase separation in the membrane. We now present results of our study of the Ca2+ uptake kinetics and of the structure of the SR membrane at low [Mg2+] (less than or equal to 100 microM). Our results show a slowing in the kinetics of both phases of the Ca2+ uptake process and an increase in the duration of the plateau of the fast phase before the onset of the slow phase, indicating an increase in the lifetime (transient trapping) of E1 approximately P. Calcium uptake kinetics at low [Mg2+] and moderately low temperature (approximately 0 degree C) are similar to those observed at much lower temperatures (approximately -10 degrees C) at high [Mg2+]. The temperature-induced structural changes that we observed at low [Mg2+] are much more pronounced than those found to occur at higher [Mg2+]. Also, at the lower [Mg2+] the upper characteristic temperature th for lipid lateral phase separation was found to be higher, at approximately 8-10 degrees C. Our studies indicate that both temperature and [Mg2+] affect the structure and the functionality (as measured by changes in the kinetics of Ca2+ uptake) of the SR membrane. Membrane lipid phase behavior and changes in the Ca2+ ATPase profile structure seem to be related, and we have found that structural changes are responsible for the slowing of the kinetics of the fast phase of Ca2+ uptake, and could also mediate the effect that [Mg2+] has on E1 approximately P lifetime.
对肌浆网(SR)Ca2+ATP酶磷酸化的直接测量表明,在Ca2+转运循环中第一个磷酸化中间体E1≈P的寿命随[Mg2+]降低而增加(杜邦,Y. 1980.《欧洲生物化学杂志》109:231 - 238)。先前在高[Mg2+]条件(25 mM)下的X射线衍射研究(帕斯科利尼,D.,和J.K. 布拉西。1988.《生物物理杂志》54:669 - 678)表明,SR膜轮廓结构的变化可能是导致在低于2 - 3摄氏度(膜中脂质横向相分离的上特征温度th)时E1≈P低温瞬时捕获的原因。我们现在展示在低[Mg2+](小于或等于100 microM)条件下对Ca2+摄取动力学和SR膜结构的研究结果。我们的结果显示Ca2+摄取过程两个阶段的动力学均减慢以及慢相开始前快相平台期持续时间增加,表明E1≈P的寿命(瞬时捕获)增加。低[Mg2+]和适度低温(约0摄氏度)下的钙摄取动力学与高[Mg2+]时在低得多的温度(约 - 10摄氏度)下观察到的相似。我们在低[Mg2+]时观察到的温度诱导结构变化比在高[Mg2+]时更明显。此外,在较低[Mg2+]时,脂质横向相分离的上特征温度th较高,约为8 - 10摄氏度。我们的研究表明温度和[Mg2+]都影响SR膜的结构和功能(通过Ca2+摄取动力学变化来衡量)。膜脂质相行为和Ca2+ATP酶轮廓结构变化似乎相关,并且我们发现结构变化是Ca2+摄取快相动力学减慢的原因,并且还可能介导[Mg2+]对E1≈P寿命的影响。