Cryobiofrontier Research Center, Faculty of Agriculture, Iwate University, 3-18-8 Ueda, Morioka, 020-8550 Iwate, Japan.
RIKEN Quantitative Biology Center, Suita, 565-0874 Osaka, Japan.
J Biochem. 2018 Apr 1;163(4):313-319. doi: 10.1093/jb/mvx083.
Spontaneous insertion of membrane proteins into liposomes formed from Escherichia coli polar phospholipids is blocked by diacylglycerol (DAG) at a physiological level. We found that cholesterol also blocks this spontaneous insertion, although a much larger amount is necessary for sufficient blockage. Reversely, sphingomyelin enhanced the spontaneous insertion. DAG at a physiological level was found not to block spontaneous insertion into liposomes formed from phosphatidylcholine (PC), while non-physiologically high concentrations of DAG reduced it. On the other hand, cholesterol blocked the spontaneous insertion into PC liposomes at a physiological level, explaining that both PC and cholesterol are absent in E. coli. While sphingomyelin did not enhance spontaneous insertion into PC liposomes, the effect of cholesterol on blockage of spontaneous insertion was dominant over that of sphingomyelin, suggesting that cholesterol functions as a blocker of disordered spontaneous insertion in eukaryotic cells. Lower amount of cholesterol was necessary to block spontaneous insertion into ER-mimic liposomes, explaining that ER membranes contain less amount of cholesterol. These results also explain that cholesterol, but not DAG, is involved in blockage of spontaneous insertion in eukaryotic cells, since DAG plays an important role as a second messenger in signal transduction.
在生理水平下,二酰基甘油(DAG)可阻断大肠杆菌极性磷脂形成的脂质体中膜蛋白的自发插入。我们发现胆固醇也能阻断这种自发插入,尽管需要更大的量才能充分阻断。相反,鞘磷脂增强了自发插入。发现生理水平的 DAG 不会阻断从磷脂酰胆碱(PC)形成的脂质体中的自发插入,而非生理水平的高浓度 DAG 则会减少这种插入。另一方面,胆固醇在生理水平下阻断了 PC 脂质体中的自发插入,这解释了大肠杆菌中既没有 PC 也没有胆固醇。虽然鞘磷脂不会增强 PC 脂质体中的自发插入,但胆固醇对自发插入阻断的影响大于鞘磷脂,表明胆固醇在真核细胞中充当无序自发插入的阻断剂。需要较少的胆固醇来阻断 ER 模拟脂质体中的自发插入,这解释了内质网膜中胆固醇的含量较低。这些结果还解释了胆固醇而不是 DAG 参与真核细胞中自发插入的阻断,因为 DAG 在信号转导中作为第二信使起着重要作用。