Chmielińska Anna, Stepien Piotr, Bonarek Piotr, Girych Mykhailo, Enkavi Giray, Rog Tomasz, Dziedzicka-Wasylewska Marta, Polit Agnieszka
Faculty of Biochemistry Biophysics and Biotechnology, Jagiellonian University, Gronostajowa 7, 30-387 Kraków, Poland.
Department of Physics, University of Helsinki, Gustaf Hällströmin katu 2, 00014 Helsinki, Finland.
Biochim Biophys Acta Biomembr. 2021 Sep 1;1863(9):183649. doi: 10.1016/j.bbamem.2021.183649. Epub 2021 May 12.
The potential-sensitive di-4-ANEPPDHQ dye is presently gaining popularity in structural studies of the lipid bilayer. Within the bilayer, dye environmental sensitivity originates from the excitation induced charge redistribution and is usually attributed to solvent relaxation. Here, di-4-ANEPPDHQ is utilized to compare the structure of neutral and negatively charged lipid bilayers between two model systems: the nanodiscs and the liposomes. Using the well-established approach of measuring solvatochromic shifts of the steady-state spectra to study the bilayer structural changes has proved insufficient in this case. By applying an in-depth analysis of time-resolved fluorescence decays and emission spectra, we distinguished and characterized two and three distinct emissive di-4-ANEPPDHQ species in the liposomes and the nanodiscs, respectively. These emissive species were ascribed to the dual emission of the dye rather than to solvent relaxation. An additional, long-lived component present in the nanodiscs was associated with a unique domain of high order, postulated recently. Our results reveal that the di-4-ANEPPDHQ steady-state fluorescence should be interpreted with caution. With the experimental approach presented here, the di-4-ANEPPDHQ sensitivity was improved. We confirmed that the bilayer structure is, indeed, altered in the nanodiscs. Moreover, molecular dynamic simulations showed a distribution of the probe in the nanodiscs plane, which is sensitive to lipid composition. In POPC nanodiscs, probe frequently interacts with MSP, while in POPC-POPG nanodiscs, such interactions are rare. We did not observe, however, any impact of those interactions on the probe fluorescence.
电位敏感染料二-4-ANEPPDHQ目前在脂质双层结构研究中越来越受欢迎。在双层膜中,染料对环境的敏感性源于激发诱导的电荷重新分布,通常归因于溶剂弛豫。在这里,二-4-ANEPPDHQ被用于比较两种模型系统(纳米盘和脂质体)中中性和带负电脂质双层的结构。在这种情况下,使用测量稳态光谱的溶剂化显色位移这一成熟方法来研究双层膜结构变化已被证明是不够的。通过对时间分辨荧光衰减和发射光谱进行深入分析,我们分别在脂质体和纳米盘中区分并表征了两种和三种不同的发射性二-4-ANEPPDHQ物种。这些发射物种归因于染料的双重发射,而非溶剂弛豫。纳米盘中存在的另一个长寿命成分与最近假设的一个独特的高阶结构域有关。我们的结果表明,二-4-ANEPPDHQ稳态荧光的解释应谨慎。通过本文介绍的实验方法,二-4-ANEPPDHQ的灵敏度得到了提高。我们证实,纳米盘中的双层膜结构确实发生了改变。此外,分子动力学模拟显示了探针在纳米盘平面内的分布,该分布对脂质组成敏感。在POPC纳米盘中,探针经常与MSP相互作用,而在POPC-POPG纳米盘中,这种相互作用很少见。然而,我们没有观察到这些相互作用对探针荧光有任何影响。