Department of Chemistry, University of British Columbia, Vancouver, British Columbia, Canada.
NanoBioPhotonics, Institute for Integrative Biology of the Cell, Université Paris-Saclay, Université Paris-Sud, CNRS, CEA, Orsay, France.
Nat Methods. 2019 Sep;16(9):815-829. doi: 10.1038/s41592-019-0530-8. Epub 2019 Aug 30.
The applications of Förster resonance energy transfer (FRET) grow with each year. However, different FRET techniques are not applied consistently, nor are results uniformly presented, which makes implementing and reproducing FRET experiments challenging. We discuss important considerations for designing and evaluating ensemble FRET experiments. Alongside a primer on FRET basics, we provide guidelines for making experimental design choices such as the donor-acceptor pair, instrumentation and labeling chemistries; selecting control experiments to unambiguously demonstrate FRET and validate that the experiments provide meaningful data about the biomolecular process in question; analyzing raw data and assessing the results; and reporting data and experimental details in a manner that easily allows for reproducibility. Some considerations are also given for FRET assays and FRET imaging, especially with fluorescent proteins. Our goal is to motivate and empower all biologists to consider FRET for the powerful research tool it can be.
荧光能量共振转移(Förster resonance energy transfer,FRET)的应用逐年增加。然而,不同的 FRET 技术并未得到一致应用,结果也未统一呈现,这使得 FRET 实验的实施和再现具有挑战性。我们讨论了设计和评估整体 FRET 实验时需要考虑的重要因素。除了 FRET 基础知识的简介外,我们还为您提供了一些指导,帮助您做出实验设计选择,例如供体-受体对、仪器和标记化学物质;选择控制实验,以明确证明 FRET,并验证实验是否提供了有关所研究生物分子过程的有意义的数据;分析原始数据并评估结果;以易于再现的方式报告数据和实验细节。我们还考虑了一些用于 FRET 测定和 FRET 成像的注意事项,特别是对于荧光蛋白。我们的目标是激励和授权所有生物学家将 FRET 作为一种强大的研究工具来考虑。