Breer H, Morris S J, Whittaker V P
Eur J Biochem. 1977 Oct 17;80(1):313-8. doi: 10.1111/j.1432-1033.1977.tb11884.x.
A rapid method for purifying Torpedo electric organ vesicles is described, which employs an isoosmotic continuous sucrose-glycine gradient followed by chromagography on CPG-10-3000 porous glass beads. The synaptic vesicles have a buoyant density of 1.057 g/ml. The purified vesicles are free of cholinesterase, lactate dehydrogenase and Na+, K+-stimulated ATPase activity. They contain a ouabaininsensitive, Na+, K+-inhibited, Mg2+, Ca2+-stimulated ATPase activity. This is further stimulated by acetylcholine but not by choline.
本文描述了一种纯化电鳐电器官囊泡的快速方法,该方法采用等渗连续蔗糖-甘氨酸梯度,随后在CPG-10-3000多孔玻璃珠上进行色谱分析。突触囊泡的浮力密度为1.057 g/ml。纯化后的囊泡不含胆碱酯酶、乳酸脱氢酶以及Na+、K+刺激的ATP酶活性。它们含有一种哇巴因不敏感、Na+、K+抑制、Mg2+、Ca2+刺激的ATP酶活性。乙酰胆碱可进一步刺激该活性,但胆碱不能。