Haigh E A, Thulborn K R, Sawyer W H
Biochemistry. 1979 Aug 7;18(16):3525-32. doi: 10.1021/bi00583a014.
Fluorescence quenching and resonance energy transfer methods have been used to investigate the position of fluorophores in the lateral and transverse planes of the lipid bilayer. A series of n-(9-anthroyloxy) fatty acids (n = 2, 6, 9, and 12) have been used as energy-transfer acceptors so that apparent transfer distances from a membrane-bound donor (N-stearoyltryptophan) have a transverse as well as a lateral component. Both theory and experiment show that the energy-transfer method is not precise enough to discriminate between the positions of the fluorophores in the transverse plane of the bilayer. The n-(9-anthroyloxy) fatty acids are also susceptible to quenching by the indole moiety of tryptophan. The relative quenching efficiency can provide a semiquantitative measure of the position of quenching molecules in the lipid bilayer. The quenching techniques are applied to the determination of the orientation of gramicidin A in lipid bilayers. The tryptophan residues of gramicidin appear to be located near the membrane surface in agreement with the head-to-head dimeric structure proposed by D. W. Urry et al. [(1971) Proc. Natl. Acad. Sci. U.S.A. 68, 672--676].
荧光猝灭和共振能量转移方法已被用于研究荧光团在脂质双层横向和纵向平面中的位置。一系列n-(9-蒽氧基)脂肪酸(n = 2、6、9和12)已被用作能量转移受体,以便从膜结合供体(N-硬脂酰色氨酸)的表观转移距离具有横向和纵向分量。理论和实验均表明,能量转移方法不够精确,无法区分荧光团在双层横向平面中的位置。n-(9-蒽氧基)脂肪酸也容易被色氨酸的吲哚部分猝灭。相对猝灭效率可以提供脂质双层中猝灭分子位置的半定量测量。猝灭技术应用于确定短杆菌肽A在脂质双层中的取向。短杆菌肽的色氨酸残基似乎位于膜表面附近,这与D. W. Urry等人提出的头对头二聚体结构一致。[(1971年)美国国家科学院院刊68,672 - 676]