Chatelain P, Berliner C, Ruysschaert J M, Jaffé J
Biochim Biophys Acta. 1976 Feb 6;419(3):540-6. doi: 10.1016/0005-2736(76)90264-9.
AC-3579 (2-N-methylpiperazinomethyl-1,3-diazafluoranthen 1-oxide) produces in rat hepatocytes a hypertrophy of the endoplasmic reticulum. Two possibilities that can explain this phenomenon are (1) that AC-3579 inactivates the phospholipases, and (2) that an AC-3579-lipid interaction hinders the enzymic activity. To demonstrate these hypotheses, a physicochemical model of biological membrane, the lipid-water interface, has been used. Dipalmitoyl DL-alpha-phosphatidyl-choline was spread at the air-water interface, the enzymes (phospholipase A or phospholipase C) dissolved in the aqueous phase. The enzymic reaction was first studied with and without AC-3579 dissolved in the aqueous phase; no enzymic inactivation was observed. However an AC-3579-lipid complex completely inhibited the enzymic reaction in the case of phospholipase A. An explanation is given in terms of steric hindrance to the enzyme-substrate.
AC - 3579(2 - N - 甲基哌嗪甲基 - 1,3 - 二氮杂荧蒽1 - 氧化物)可使大鼠肝细胞的内质网肥大。有两种可能解释这一现象的情况:(1)AC - 3579使磷脂酶失活;(2)AC - 3579与脂质的相互作用阻碍了酶活性。为了验证这些假设,采用了生物膜的物理化学模型——脂质 - 水界面。将二棕榈酰DL - α - 磷脂酰胆碱铺展在空气 - 水界面,酶(磷脂酶A或磷脂酶C)溶解于水相。首先研究了水相中溶解有和没有AC - 3579时的酶促反应;未观察到酶失活。然而,在磷脂酶A的情况下,AC - 3579 - 脂质复合物完全抑制了酶促反应。从空间位阻对酶 - 底物的影响方面给出了解释。