Wallace Bram, Atzberger Paul J
Department of Mathematics, University of California Santa Barbara, Santa Barbara, CA, 93106, United States of America.
Department of Mechanical Engineering, University of California Santa Barbara, Santa Barbara, CA, 93106, United States of America.
PLoS One. 2017 May 19;12(5):e0177122. doi: 10.1371/journal.pone.0177122. eCollection 2017.
Förster resonance energy transfer (FRET) is a widely used single-molecule technique for measuring nanoscale distances from changes in the non-radiative transfer of energy between donor and acceptor fluorophores. For macromolecules and complexes this observed transfer efficiency is used to infer changes in molecular conformation under differing experimental conditions. However, sometimes shifts are observed in the FRET efficiency even when there is strong experimental evidence that the molecular conformational state is unchanged. We investigate ways in which such discrepancies can arise from kinetic effects. We show that significant shifts can arise from the interplay between excitation kinetics, orientation diffusion of fluorophores, separation diffusion of fluorophores, and non-emitting quenching.
荧光共振能量转移(FRET)是一种广泛应用的单分子技术,用于通过供体和受体荧光团之间非辐射能量转移的变化来测量纳米尺度的距离。对于大分子和复合物,这种观察到的转移效率用于推断不同实验条件下分子构象的变化。然而,有时即使有强有力的实验证据表明分子构象状态未发生变化,FRET效率也会出现偏移。我们研究了这种差异可能由动力学效应产生的方式。我们表明,显著的偏移可能源于激发动力学、荧光团的取向扩散、荧光团的分离扩散以及非发射猝灭之间的相互作用。