Storch J, Kleinfeld A M
Biochemistry. 1986 Apr 8;25(7):1717-26. doi: 10.1021/bi00355a041.
Movement of free fatty acids (ffa) between small unilamellar vesicles (SUV) was studied by measuring the transfer of fluorescent n-(9-anthroyloxy)-labeled analogues (AOffa) between donor and acceptor vesicles. Donors were composed of egg phosphatidylcholine (PC) loaded with 1-2 mol % AOffa, and acceptors were egg PC containing 10-12 mol % N-(7-nitro-2,1,3-benzoxadiazol-4-yl)phosphatidylethanolamine (NBD-PE). The fluorescence of AO added directly to acceptor SUV was greater than 98% quenched by energy transfer to NBD. Thus, AOffa movement from donor to acceptor was monitored by the time-dependent decrease in AO fluorescence. The transfer of the short-chain AOffa, although too fast to be resolved by the methods used here, is consistent with studies that find transfer rates on the order of milliseconds and kinetics which are first order. In contrast, transfer rates for the long-chain AOffa are more than 2 orders of magnitude slower, and the kinetics of the transfer process are best described by the sum of two exponentials plus a constant. The ffa ionization state was also found to be an important determinant of transfer rate. The charged species transferred an average of 10-fold faster than the protonated ffa. The ffa pKa in the membrane is 9, as calculated from the pH dependence of transfer. Similar to results found for other lipids, long-chain AOffa are transferred via water rather than a collision-mediated process. The aqueous phase route of AOffa intermembrane transfer is indicated by the lack of effect on transfer of large alterations in the product of donor and acceptor phospholipid concentrations. Moreover, the transfer rate is decreased as [NaCl] is increased from 0.1 to 4 M. This effect of ionic strength is probably due not only to a decrease in the aqueous phase partition of the AOffa but also to an alteration in bilayer structure, as measured by fluorescence polarization of 1,6-diphenyl-1,3,5-hexatriene. The observed kinetics are consistent with a model in which the transfer involves two steps: transbilayer movement between the inner and outer bilayer leaflets, followed by transfer from the outer leaflet to the aqueous phase (off rate). Within the framework of this model, the observed slow rate is primarily determined by the rate of transbilayer movement, and the observed fast rate is approximately equal to the off rate. The off rate is about 10-fold faster than the rate of transbilayer movement.
通过测量荧光N-(9-蒽氧基)标记类似物(AOffa)在供体囊泡和受体囊泡之间的转移,研究了游离脂肪酸(ffa)在小单层囊泡(SUV)之间的移动。供体由负载1 - 2摩尔% AOffa的鸡蛋磷脂酰胆碱(PC)组成,受体是含有10 - 12摩尔% N-(7-硝基-2,1,3-苯并恶二唑-4-基)磷脂酰乙醇胺(NBD-PE)的鸡蛋PC。直接添加到受体SUV中的AO荧光通过能量转移到NBD而猝灭超过98%。因此,通过AO荧光随时间的降低来监测AOffa从供体到受体的移动。短链AOffa的转移虽然太快以至于无法用这里使用的方法分辨,但与发现转移速率在毫秒量级且动力学为一级的研究一致。相比之下,长链AOffa的转移速率慢了2个多数量级,转移过程的动力学最好用两个指数加一个常数的和来描述。还发现ffa的电离状态是转移速率的一个重要决定因素。带电物种的转移平均比质子化ffa快10倍。根据转移对pH的依赖性计算,膜中ffa的pKa为9。与其他脂质的结果相似,长链AOffa是通过水而不是碰撞介导的过程进行转移的。AOffa跨膜转移的水相途径由供体和受体磷脂浓度乘积的大幅变化对转移没有影响表明。此外,随着[NaCl]从0.1 M增加到4 M,转移速率降低。离子强度的这种影响可能不仅是由于AOffa在水相分配的减少,还由于双层结构的改变,这通过1,6-二苯基-1,3,5-己三烯的荧光偏振来测量。观察到的动力学与一个模型一致,在该模型中转移涉及两个步骤:在内层和外层双层小叶之间的跨双层移动,然后从外层小叶转移到水相(解离速率)。在这个模型的框架内,观察到的慢速主要由跨双层移动的速率决定,观察到的快速速率大约等于解离速率。解离速率比跨双层移动的速率快约10倍。