Wilson B W, Nieberg P S
Biochem Pharmacol. 1983 Mar 1;32(5):911-8. doi: 10.1016/0006-2952(83)90596-8.
Studies of recovery of acetylcholinesterase (AChE, EC 3.1.1.7) after inhibition by organophosphates (OPs) have been hampered by the low number of in vitro systems with large collagen-tailed forms of AChE characteristic of motor end plates. Pectoral muscle cultures from Japanese quail with high levels of a large 20S form of AChE were used to study recovery of cells from acute treatment with diisopropylfluorophosphate (DFP), an irreversible AChE inhibitor. Low molecular weight AChE forms were synthesized more rapidly than the large 20S form following a 15-min treatment with 10(-4)M DFP. Most of the activities of the small forms, but only part of the activity of the 20S form, disappeared within 48 hr after cycloheximide was added to block protein synthesis. To the contrary, virtually all the activity of the 20S AChE that was newly synthesized after DFP treatment was lost within 24 hr after cycloheximide treatment. The results were generally consistent with the idea that the 20S AChE form is assembled inside the cell near to its surface and then is released to bind to its outside.
有机磷酸酯(OPs)抑制后乙酰胆碱酯酶(AChE,EC 3.1.1.7)恢复的研究受到阻碍,因为具有运动终板特征的大胶原尾型AChE的体外系统数量较少。来自日本鹌鹑的胸肌培养物中含有高水平的20S大形式AChE,用于研究用不可逆的AChE抑制剂二异丙基氟磷酸酯(DFP)急性处理后细胞的恢复情况。在用10(-4)M DFP处理15分钟后,低分子量AChE形式的合成速度比20S大形式更快。添加环己酰亚胺以阻断蛋白质合成后,小形式的大部分活性在48小时内消失,但20S形式的活性仅部分消失。相反,DFP处理后新合成的20S AChE的几乎所有活性在环己酰亚胺处理后24小时内丧失。结果总体上与以下观点一致,即20S AChE形式在细胞内靠近其表面组装,然后释放以结合到其外部。