Fontaine Nicolas, Harter Lara, Marette André, Boudreau Denis
Department of Chemistry, Université Laval, 1045 avenue de la Médecine, Québec, CanadaG1V 0A6.
Center for Optics, Photonics and Lasers, Université Laval, 2375 rue de la Terrasse, Québec, CanadaG1V 0A6.
ACS Omega. 2022 Dec 28;8(1):1067-1078. doi: 10.1021/acsomega.2c06420. eCollection 2023 Jan 10.
Lysophosphatidic acids (LPA) are key biomarkers for several physiological processes, the monitoring of which can provide insights into the host's health. Common lab-based techniques for their detection are cumbersome, expensive, and necessitate specialized personnel to operate. LPA-sensitive fluorescent probes have been described, albeit for nonaqueous conditions, which impedes their use in biological matrices. In this paper, we explore in detail the influence of structure on the extent of aggregation-induced fluorescence quenching using specially synthesized styrylpyridinium dyes bearing structural adaptations to bestow them enhanced affinity toward LPA in aqueous media. Spectroscopic investigations supported by time-resolved fluorimetry revealed the contribution of excimer formation to the fluorescence quenching mechanism displayed by the fluorescent probes. Experimental observations of the influence of structure on detection sensitivity were supported by DFT calculations.
溶血磷脂酸(LPA)是多种生理过程的关键生物标志物,对其进行监测可以深入了解宿主的健康状况。常用的基于实验室的检测技术繁琐、昂贵,且需要专业人员操作。虽然已经报道了对LPA敏感的荧光探针,但这些探针仅适用于非水条件,这限制了它们在生物基质中的应用。在本文中,我们详细探讨了结构对聚集诱导荧光猝灭程度的影响,使用了经过特殊合成的苯乙烯基吡啶鎓染料,这些染料具有结构适应性,使其在水性介质中对LPA具有更高的亲和力。时间分辨荧光光谱研究支持的光谱研究揭示了准分子形成对荧光探针显示的荧光猝灭机制的贡献。密度泛函理论(DFT)计算支持了结构对检测灵敏度影响的实验观察结果。