Rossi J P, Garrahan P J, Rega A F
J Membr Biol. 1978 Dec 8;44(1):37-46. doi: 10.1007/BF01940572.
Human red cells containing low ATP and high Pi concentrations were suspended in media with and without 2 mM Ca2+, and the incorporation of (32P)Pi into ATP was measured. There was some incorporation whatever the medium, but in every experiment there was an extra incorporation when the cells were in the Ca2+-containing medium. This extra incorporation was abolished by the ionophore A23187, which collapses the Ca2+ concentration gradient across the membranes, or by LaCl3, which blocks the Ca2+ pump. Starved and phosphate-loaded cells also show an uptake of Ca2+ which is not apparent in fresh cells. Results are consistent with the idea that Ca2+-dependent incorporation of Pi into ATP is catalyzed by the Ca2+ pump using energy derived from the Ca2+ concentration gradient.
将含有低ATP和高无机磷酸盐(Pi)浓度的人体红细胞悬浮于含有和不含2 mM钙离子(Ca2+)的培养基中,并测定(32P)Pi掺入ATP的情况。无论培养基如何,都会有一定程度的掺入,但在每个实验中,当细胞处于含Ca2+的培养基中时,都会有额外的掺入。这种额外的掺入被离子载体A23187消除,A23187会破坏跨膜的Ca2+浓度梯度,或者被氯化镧(LaCl3)消除,LaCl3会阻断Ca2+泵。饥饿且加载了磷酸盐的细胞也表现出对Ca2+的摄取,而这在新鲜细胞中并不明显。结果与以下观点一致,即依赖Ca2+的Pi掺入ATP是由Ca2+泵催化的,该过程利用了来自Ca2+浓度梯度的能量。