Department of Chemistry, Michigan Technological University, Houghton, Michigan 49931, United States.
Department of Biological Science, Michigan Technological University, Houghton, Michigan 49931, United States.
ACS Appl Bio Mater. 2024 Aug 19;7(8):5437-5451. doi: 10.1021/acsabm.4c00595. Epub 2024 Jul 12.
Fluorescent probes play a crucial role in elucidating cellular processes, with NAD(P)H sensing being pivotal in understanding cellular metabolism and redox biology. Here, the development and characterization of three fluorescent probes, , , and , based on the coumarin platform for monitoring of NAD(P)H levels in living cells are described. Probes and incorporate a coumarin-cyanine hybrid structure with vinyl and thiophene connection bridges to 3-quinolinium acceptors, respectively, while probe introduces a dicyano moiety for replacement of the lactone carbonyl group of probe which increases the reaction rate of the probe with NAD(P)H. Initially, all probes exhibit subdued fluorescence due to intramolecular charge transfer (ICT) quenching. However, upon hydride transfer by NAD(P)H, fluorescence activation is triggered through enhanced ICT. Theoretical calculations confirm that the electronic absorption changes upon the addition of hydride to originate from the quinoline moiety instead of the coumarin section and end up in the middle section, illustrating how the addition of hydride affects the nature of this absorption. Control and dose-response experiments provide conclusive evidence of probe 's specificity and reliability in identifying intracellular NAD(P)H levels within HeLa cells. Furthermore, colocalization studies indicate probe 's selective targeting of mitochondria. Investigation into metabolic substrates reveals the influence of glucose, maltose, pyruvate, lactate, acesulfame potassium, and aspartame on NAD(P)H levels, shedding light on cellular responses to nutrient availability and artificial sweeteners. Additionally, we explore the consequence of oxaliplatin on cellular NAD(P)H levels, revealing complex interplays between DNA damage repair, metabolic reprogramming, and enzyme activities. In vivo studies utilizing starved fruit fly larvae underscore probe 's efficacy in monitoring NAD(P)H dynamics in response to external compounds. These findings highlight probe 's utility as a versatile tool for investigating NAD(P)H signaling pathways in biomedical research contexts, offering insights into cellular metabolism, stress responses, and disease mechanisms.
荧光探针在阐明细胞过程中起着至关重要的作用,其中 NAD(P)H 感应对于理解细胞代谢和氧化还原生物学至关重要。在这里,描述了基于香豆素平台的三种荧光探针 、 、 和 的开发和表征,用于监测活细胞中的 NAD(P)H 水平。探针 和 分别采用香豆素-氰基杂化结构,带有乙烯基和噻吩连接桥,以 3-喹啉受体为受体,而探针 则引入了二氰基部分,取代探针 的内酯羰基,这增加了探针与 NAD(P)H 的反应速率。最初,由于分子内电荷转移 (ICT) 猝灭,所有探针都表现出较弱的荧光。然而,当 NAD(P)H 发生氢转移时,通过增强 ICT 触发荧光激活。理论计算证实,加氢引起的电子吸收变化源于喹啉部分,而不是香豆素部分,最终出现在中间部分,说明加氢如何影响这种吸收的性质。对照和剂量反应实验提供了确凿的证据,证明探针 在识别 HeLa 细胞内细胞内 NAD(P)H 水平方面的特异性和可靠性。此外,共定位研究表明探针 选择性靶向线粒体。对代谢底物的研究揭示了葡萄糖、麦芽糖、丙酮酸、乳酸、乙酰磺胺酸钾和阿斯巴甜对 NAD(P)H 水平的影响,阐明了细胞对营养物质可用性和人工甜味剂的反应。此外,我们还研究了奥沙利铂对细胞 NAD(P)H 水平的影响,揭示了 DNA 损伤修复、代谢重编程和酶活性之间的复杂相互作用。利用饥饿的果蝇幼虫进行的体内研究强调了探针 在监测对外界化合物的 NAD(P)H 动力学反应中的功效。这些发现突出了探针 在生物医学研究背景下作为研究 NAD(P)H 信号通路的多功能工具的效用,为细胞代谢、应激反应和疾病机制提供了深入的见解。