Mazères S, Schram V, Tocanne J F, Lopez A
Laboratoire de Pharmacologie et Toxicologie Fondamentales du CNRS, Department III, Toulouse, France.
Biophys J. 1996 Jul;71(1):327-35. doi: 10.1016/S0006-3495(96)79228-7.
Steady-state and time-resolved fluorescence properties of the 7-nitrobenz-2-oxa-1, 3-diazole-4-yl (NBD) fluorophore attached either to the sn-2 acyl chain of various phospholipids (phosphatidylcholine, phosphatidylethanolamine, phosphatidylserine, and phosphatidic acid) or to the polar headgroup of phosphatidylethanolamine were studied after insertion of these NBD-labeled lipid probes into unilamellar vesicles of phosphatidylcholine, phosphatidylglycerol, phosphatidic acid, and phosphatidylserine. The fluorescence response of the NBD group was observed to strongly depend on the chemical structure and physical state of the host phospholipids and on the chemical structure of the lipid probe itself. Among the various fluorescence parameters studied, i.e., Stokes' shifts, lifetimes, and quantum yields, the quantum yields were by far the most affected by these structural and environmental factors, whereas the Stokes' shifts were practically unaffected. Thus, depending on the phospholipid probe and the host phospholipid, the fluorescence emission of the NBD group was found to vary by a factor of up to 5. Careful analysis of the data shows that for the various couples of probe and host lipid molecules studied, deexcitation of the fluorophore was dominated by nonradiative deactivation processes. This great sensitivity of the NBD group to environmental factors originates from its well-known solvatochromic properties, and comparison of these knr values with those obtained for n-propylamino-NBD in a set of organic solvents covering a large scale of polarity indicates that in phospholipids, the NBD fluorophore experiences a dielectric constant of around 27-41, corresponding to a medium of relatively high polarity. From these epsilon values and on the basis of models of the dielectric transition that characterizes any water-phospholipid interface, it can be inferred that for all of the phospholipid probes and host phospholipids tested, the NBD group is located in the region of the polar headgroups, near the phosphoglycerol moiety of the lipids.
将连接有7-硝基苯并-2-恶唑-1,3-二唑-4-基(NBD)荧光团的磷脂(磷脂酰胆碱、磷脂酰乙醇胺、磷脂酰丝氨酸和磷脂酸)的sn-2酰基链或连接到磷脂酰乙醇胺的极性头部基团,插入磷脂酰胆碱、磷脂酰甘油、磷脂酸和磷脂酰丝氨酸的单层囊泡后,研究了其稳态和时间分辨荧光特性。观察到NBD基团的荧光响应强烈依赖于主体磷脂的化学结构和物理状态以及脂质探针本身的化学结构。在所研究的各种荧光参数中,即斯托克斯位移、寿命和量子产率,量子产率受这些结构和环境因素的影响最大,而斯托克斯位移实际上不受影响。因此,根据磷脂探针和主体磷脂的不同,发现NBD基团的荧光发射变化高达5倍。对数据的仔细分析表明,对于所研究的各种探针和主体脂质分子对,荧光团的去激发主要由非辐射失活过程主导。NBD基团对环境因素的这种高度敏感性源于其众所周知的溶剂化显色特性,将这些knr值与在一系列极性范围广泛的有机溶剂中获得的正丙基氨基-NBD的值进行比较表明,在磷脂中,NBD荧光团经历的介电常数约为27-41,对应于极性相对较高的介质。根据这些ε值,并基于表征任何水-磷脂界面的介电跃迁模型,可以推断,对于所有测试的磷脂探针和主体磷脂,NBD基团位于极性头部基团区域,靠近脂质的磷酸甘油部分。