Department of Biophysics and Cell Biology, University of Debrecen, 98 Nagyerdei krt., H-4032 Debrecen, Hungary.
Chemphyschem. 2010 Dec 3;11(17):3713-21. doi: 10.1002/cphc.201000568.
Fluorescence resonance energy transfer (FRET) is a strongly distance-dependent process between a donor and an acceptor molecule, which can be used for sensitive distance measurements and characterization of molecular interactions at the nanometer level. The original mathematical description of this process, however, is only valid for the interaction of one donor with one acceptor. This criterion is not always met, especially in biological systems, where multiple structures can interact simultaneously, often making distance estimations based on transfer efficiency values error-prone. Herein we investigate how the interaction of multiple acceptors and donors influences the transfer efficiency value in an intramolecular cellular FRET system by manipulating the fluorophore/protein ratio of the fluorophore-conjugated antibodies. We show that the labeling ratio of the acceptor has the largest influence on measured transfer efficiency and decreasing or increasing the acceptor labeling ratio can be utilized to manipulate the FRET response of the acceptor-donor pair and therefore is a tool for optimizing sensitivity of FRET measurements.
荧光共振能量转移(FRET)是供体和受体分子之间强烈依赖于距离的过程,可用于纳米级距离测量和分子相互作用的特征描述。然而,该过程的原始数学描述仅适用于一个供体与一个受体的相互作用。这个标准并不总是满足的,特别是在生物系统中,多个结构可以同时相互作用,这使得基于转移效率值的距离估计容易出错。在此,我们通过操纵荧光素标记的抗体的荧光素/蛋白质比,研究了多个供体和受体的相互作用如何影响细胞内分子 FRET 系统中的转移效率值。我们表明,受体的标记比对接收到的转移效率有最大的影响,并且可以减少或增加受体的标记比,以操纵供体-受体对的 FRET 响应,因此是优化 FRET 测量灵敏度的工具。