Zammit V A, Corstorphine C G, Kolodziej M P, Fraser F
Hannah Research Institute, Ayr, Scotland, United Kingdom.
Lipids. 1998 Apr;33(4):371-6. doi: 10.1007/s11745-998-0217-7.
Mitochondrial outer membranes were prepared from livers of rats that were in the normal fed state, starved for 48 h, or made diabetic by injection of streptozotocin. Membranes were also prepared from starved late-pregnant rats. The latter three conditions have previously been shown to induce varying degrees of desensitization of mitochondrial overt carnitine palmitoyltransferase (CPT I) to malonyl-CoA inhibition. We measured the fluorescence polarization anisotropy of two probes, 1,6-diphenyl-1,3,5-hexatriene (DPH) and 1-(4-trimethylammoniumphenyl)-6-phenyl-1,3,5-hexatriene-p-toluenes ulfonate (TMA-DPH) which, when incorporated into membranes, report on the hydrophobic core and on the peripheral regions of the bilayer, respectively. The corresponding polarization indices (rDPH and rTMA-DPH) were calculated. In membranes of all three conditions characterized by CPT I desensitization to malonyl-CoA, rDPH was decreased, whereas there was no change in rTMA-DPH, indicating that CPT I is sensitive to changes in membrane core, rather than peripheral, lipid order. The major lipid components of the membranes were analyzed. Although significant changes with physiological state were observed, there was no consistent pattern of changes in gross lipid composition accompanying the changes to membrane fluidity and CPT I sensitivity to malonyl-CoA. We conclude that CPT I kinetic characteristics are sensitive to changes in lipid composition that are localized to specific membrane microdomains.
线粒体外膜取自处于正常进食状态、饥饿48小时或通过注射链脲佐菌素诱导糖尿病的大鼠肝脏。也从饥饿的妊娠晚期大鼠制备了线粒体外膜。先前已表明,后三种情况会导致线粒体表面肉碱棕榈酰转移酶(CPT I)对丙二酰辅酶A抑制的脱敏程度不同。我们测量了两种探针1,6-二苯基-1,3,5-己三烯(DPH)和1-(4-三甲基铵苯基)-6-苯基-1,3,5-己三烯对甲苯磺酸盐(TMA-DPH)的荧光偏振各向异性,当它们掺入膜中时,分别报告疏水核心和双层的外围区域。计算了相应的偏振指数(rDPH和rTMA-DPH)。在所有三种以CPT I对丙二酰辅酶A脱敏为特征的情况下,膜中的rDPH均降低,而rTMA-DPH没有变化,这表明CPT I对膜核心而非外围脂质有序性的变化敏感。分析了膜的主要脂质成分。虽然观察到随生理状态有显著变化,但在总体脂质组成上没有伴随膜流动性和CPT I对丙二酰辅酶A敏感性变化的一致变化模式。我们得出结论,CPT I的动力学特征对定位于特定膜微区的脂质组成变化敏感。