Shieh D D, Ueda I, Lin H, Eyring H
Proc Natl Acad Sci U S A. 1976 Nov;73(11):3999-4002. doi: 10.1073/pnas.73.11.3999.
Sonicated 1,2-dihexadecyl-sn-glycero-3-phosphorylcholine forms liposomes. Studies by Fourier transform proton magnetic resonance of the interaction of these bilayers with some general anesthetics, i.e., chloroform, halothane, methoxyflurane, and enflurane, show that the addition of a general anesthetic to the liposomes and raising the temperature have a similar effect in cuasing the fluidization of the bilayer. General anesthetics act on the hydrophilic site (choline group) in clinical concentrations and then diffuse into the hydrophobic region with the addition of larger amount of anesthetics. There is evidence that the lecithin choline groups are involved in the interaction with protein and that the general anesthetics change the conformation of some polypeptides and proteins. We conclude that the general anesthetics, by increasing the motion of positively charged choline groups and negatively charged groups in protein, weaken the Coulomb-type interaction and cause the liprotein conformational changes.
超声处理的1,2 - 二正十六烷基 - sn - 甘油 - 3 - 磷酸胆碱形成脂质体。通过傅里叶变换质子磁共振研究这些双层膜与一些全身麻醉剂(即氯仿、氟烷、甲氧氟烷和恩氟烷)的相互作用表明,向脂质体中添加全身麻醉剂并升高温度在导致双层膜流化方面具有相似的效果。全身麻醉剂在临床浓度下作用于亲水位点(胆碱基团),然后随着麻醉剂用量增加扩散到疏水区域。有证据表明卵磷脂胆碱基团参与与蛋白质的相互作用,并且全身麻醉剂会改变一些多肽和蛋白质的构象。我们得出结论,全身麻醉剂通过增加蛋白质中带正电荷的胆碱基团和带负电荷基团的运动,削弱库仑型相互作用并导致脂蛋白构象变化。