Kozlov I A, Vulfson E N
FEBS Lett. 1985 Mar 25;182(2):425-8. doi: 10.1016/0014-5793(85)80347-1.
The interaction of inorganic phosphate with native and nucleotide-depleted F1-ATPase was studied. F1-ATPase depleted of tightly bound nucleotides loses the ability to bind inorganic phosphate. The addition of ATP, ADP, GTP and GDP but not AMP, restores the phosphate binding. The nucleotides affecting the phosphate binding to F1-ATPase are located at the catalytic (exchangeable) site of the enzyme. The phosphate is thought to bind to the same catalytic site where the nucleotide is already bound. It is thought that ADP is the first substrate to bind to F1-ATPase in the ATP synthesis reaction.
研究了无机磷酸盐与天然及核苷酸耗尽的F1-ATP酶之间的相互作用。耗尽紧密结合核苷酸的F1-ATP酶失去了结合无机磷酸盐的能力。添加ATP、ADP、GTP和GDP(但不是AMP)可恢复磷酸盐结合能力。影响磷酸盐与F1-ATP酶结合的核苷酸位于该酶的催化(可交换)位点。磷酸盐被认为与核苷酸已结合的同一催化位点结合。据认为,在ATP合成反应中,ADP是第一个与F1-ATP酶结合的底物。