Greenhut S F, Roseman M A
Biochemistry. 1985 Feb 26;24(5):1252-60. doi: 10.1021/bi00326a030.
Cytochrome b5 induced flip-flop of phosphatidylethanolamine (PE) in sonicated vesicles prepared from a 9:1 mixture of phosphatidylcholine (PC) to phosphatidylethanolamine was determined as follows. First, vesicles having a nonequilibrium distribution of PE across the bilayer were prepared by amidinating the external amino groups with isethionyl acetimidate. Amidinated cytochrome b5 was then added, and after the protein was completely bound, the rate of appearance of fresh PE on the outer surface was determined by removing aliquots at timed intervals and titrating the external amino groups with trinitrobenzenesulfonic acid. The results show an initial rapid phase of flip-flop (especially in the presence of salt) followed by a very slow phase, at 25 degrees C. Similar results were obtained when cytochrome b5 was introduced into the amidinated vesicles by spontaneous transfer from PC donor vesicles. These results indicate that the accumulation of the transferable ("loose") form of cytochrome b5 on the outer surface of a vesicle causes a transient, global destabilization of the bilayer that is relieved by lipid flip-flop. We speculate that this mechanism may be a significant driving force for the transfer of amphipathic molecules across membranes.
细胞色素b5诱导由磷脂酰胆碱(PC)与磷脂酰乙醇胺按9:1比例混合制备的超声处理囊泡中磷脂酰乙醇胺(PE)的翻转情况如下测定。首先,通过用羟乙磺酰乙亚胺酰胺化外部氨基来制备PE在双层中分布不均的囊泡。然后加入酰胺化的细胞色素b5,在蛋白质完全结合后,通过定时取出等分试样并用三硝基苯磺酸滴定外部氨基来测定外表面上新PE出现的速率。结果显示在25℃时,翻转有一个初始快速阶段(特别是在有盐存在时),随后是一个非常缓慢的阶段。当细胞色素b5通过从PC供体囊泡自发转移引入酰胺化囊泡时,也得到了类似结果。这些结果表明,可转移(“松散”)形式的细胞色素b5在囊泡外表面的积累会导致双层膜的瞬时整体不稳定,这种不稳定通过脂质翻转得以缓解。我们推测这种机制可能是两亲性分子跨膜转运的一个重要驱动力。