Jones G M, Wofsy C, Aurell C, Sklar L A
Department of Pathology, The University of New Mexico, Albuquerque, New Mexico 87131, USA.
Biophys J. 1999 Jan;76(1 Pt 1):517-27. doi: 10.1016/S0006-3495(99)77220-6.
Fluorescence resonance energy transfer (FRET) measurements have been used to analyze fluorophore separations in a number of varying geometries, including small particles and extended surfaces. This study focuses on the geometry created by a donor extended above the surface of a small sphere (radius < R0), where the acceptors are integrated into the sphere surface. The model of this geometry was based on an amphipathic molecule with its lipophilic region integrated into a detergent micelle and its hydrophilic region extending outward from the micelle surface, where the donor fluorophore is attached to the hydrophilic region of the molecule. Based on random acceptor incorporation into the micelle, a Poisson distribution was used to calculate the distribution of acceptor probes across the micelle population. The model converges to RET on a flat surface when the radius of the micelle exceeds 0.8 R0. The model was also used to simulate FRET data showing that the positions of donors above the micelle surface could be uniquely resolved. Experimental verification of the model was achieved in a sulfobetaine palmitate micelle with fluorescein isothiocyanate donors attached to detergent-solubilized lipopolysaccharide (LPS) and lipophilic Fast-DiI acceptors. The use of steady-state analysis allowed resolution of cases in which donors were located at different distances from the surface. Combining steady-state with excited-state lifetime analysis allowed resolution of cases where there was a combination of distances. Given the large number of biomolecules that interact with lipids, this approach may prove generally useful for defining molecular conformation.
荧光共振能量转移(FRET)测量已被用于分析多种不同几何结构中的荧光团分离情况,包括小颗粒和扩展表面。本研究聚焦于由一个供体在小球体(半径 < R0)表面上方延伸所形成的几何结构,其中受体整合到球体表面。这种几何结构的模型基于一种两亲分子,其亲脂区域整合到去污剂胶束中,亲水区域从胶束表面向外延伸,供体荧光团连接到该分子的亲水区域。基于受体随机掺入胶束的情况,使用泊松分布来计算受体探针在整个胶束群体中的分布。当胶束半径超过0.8 R0时,该模型收敛于平面上的RET。该模型还用于模拟FRET数据,表明供体在胶束表面上方的位置可以唯一确定。在具有连接到去污剂增溶的脂多糖(LPS)上的异硫氰酸荧光素供体和亲脂性Fast-DiI受体的棕榈酸磺基甜菜碱胶束中实现了对该模型的实验验证。使用稳态分析可以分辨供体位于距表面不同距离的情况。将稳态分析与激发态寿命分析相结合,可以分辨存在距离组合的情况。鉴于与脂质相互作用的生物分子数量众多,这种方法可能被证明对定义分子构象普遍有用。