Fontana Mattia, Ivanovaitė Šarunė, Lindhoud Simon, van der Wijk Elmar, Mathwig Klaus, Berg Willy van den, Weijers Dolf, Hohlbein Johannes
Laboratory of Biophysics, Wageningen University and Research, Stippeneng 4, Wageningen, 6708 WE, The Netherlands.
Laboratory of Biochemistry, Wageningen University and Research, Stippeneng 4, Wageningen, 6708 WE, The Netherlands.
Adv Biol (Weinh). 2022 Apr;6(4):e2100953. doi: 10.1002/adbi.202100953. Epub 2021 Sep 2.
Single-molecule fluorescence detection offers powerful ways to study biomolecules and their complex interactions. Here, nanofluidic devices and camera-based, single-molecule Förster resonance energy transfer (smFRET) detection are combined to study the interactions between plant transcription factors of the auxin response factor (ARF) family and DNA oligonucleotides that contain target DNA response elements. In particular, it is shown that the binding of the unlabeled ARF DNA binding domain (ARF-DBD) to donor and acceptor labeled DNA oligonucleotides can be detected by changes in the FRET efficiency and changes in the diffusion coefficient of the DNA. In addition, this data on fluorescently labeled ARF-DBDs suggest that, at nanomolar concentrations, ARF-DBDs are exclusively present as monomers. In general, the fluidic framework of freely diffusing molecules minimizes potential surface-induced artifacts, enables high-throughput measurements, and proved to be instrumental in shedding more light on the interactions between ARF-DBDs monomers and between ARF-DBDs and their DNA response element.
单分子荧光检测为研究生物分子及其复杂相互作用提供了强大的方法。在此,将纳米流体装置与基于相机的单分子荧光共振能量转移(smFRET)检测相结合,以研究生长素响应因子(ARF)家族的植物转录因子与含有靶DNA响应元件的DNA寡核苷酸之间的相互作用。特别地,研究表明,通过FRET效率的变化和DNA扩散系数的变化,可以检测未标记的ARF DNA结合结构域(ARF-DBD)与供体和受体标记的DNA寡核苷酸的结合。此外,关于荧光标记的ARF-DBD的这些数据表明,在纳摩尔浓度下,ARF-DBD仅以单体形式存在。一般来说,自由扩散分子的流体框架将潜在的表面诱导伪影降至最低,实现高通量测量,并被证明有助于更深入地了解ARF-DBD单体之间以及ARF-DBD与其DNA响应元件之间的相互作用。