Fluorescent Zinc Sensors for Cellular Imaging

用于细胞成像的荧光锌传感器

• 批准号: 6808479
• 负责人: CHRISTOPH J FAHRNI
• 金额: $ 25.7万
• 依托单位: GEORGIA INSTITUTE OF TECHNOLOGY
• 依托单位国家: 美国
• 财政年份: 2004
• 资助国家: 美国
• 起止时间: 2004-08-15 至 2009-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6808479
• 关键词: X ray crystallography; cell line; chemical synthesis; chromophore; cytotoxicity; fluorescence microscopy; fluorescence spectrometry; fluorescent dye /probe; intracellular transport; ionophores; quantum chemistry; technology /technique development; thermodynamics; vesicle /vacuole; zinc

DESCRIPTION (provided by applicant): Zinc serves as a cofactor in various metallo enzymes and is involved in a broad range of biological processes, such as neurotransmission, gene expression, apoptosis, and immune system functions. Much of the intracellular zinc is bound to proteins and the concentration of free zinc in the cytoplasm is extremely low; however, a fraction of the total zinc is localized in cytoplasmic vesicles and freely exchangeable. There is strong evidence, that these vesicles play a central role in the intracellular regulation of Zn(ll) and possibly other vital biological processes. However, the nature of these processes and the biological function of the vesicles are elusive. The investigation of the dynamics of vesicular zinc has been hampered in particular by the lack of Zn(ll)-specific fluorescent probes, that are suitable for live cell studies. This proposal describes the design, synthesis and characterization of Zn(ll)-specific fluorescent probes, that should overcome problems of existing probes and enable researchers to elucidate the mechanisms of cellular zinc homeostasis. The proposed sensors are specifically designed for two-photon excitation microscopy, a noninvasive live cell imaging technique that drastically reduces photoxicity. The sensing mechanism is based on zinc-induced inhibition of excited state proton transfer (ESIPT), a new design concept that provides large spectral shifts suitable for quantitative emission ratiometric measurements. The proposed research fills a critical niche in the biological chemistry of metal ion speciation. The lack of a non-invasive zinc specific fluorescent sensor is currently a limiting factor in the study of intracellular zinc regulation and trafficking.

描述（由申请人提供）：锌作为各种金属酶的辅因子，参与广泛的生物过程，如神经传递、基因表达、细胞凋亡和免疫系统功能。大部分细胞内锌与蛋白质结合，并且细胞质中游离锌的浓度极低;然而，总锌的一部分位于细胞质囊泡中并可自由交换。有强有力的证据表明，这些囊泡在Zn（II）的细胞内调节和可能的其他重要生物过程中发挥核心作用。然而，这些过程的性质和囊泡的生物学功能是难以捉摸的。泡状锌的动力学的调查已受到阻碍，特别是缺乏锌（II）特异性荧光探针，这是适合活细胞研究。该提案描述了Zn（II）特异性荧光探针的设计、合成和表征，其应克服现有探针的问题，并使研究人员能够阐明细胞锌稳态的机制。所提出的传感器是专为双光子激发显微镜，一种非侵入性的活细胞成像技术，大大降低了光毒性。的传感机制是基于锌诱导抑制激发态质子转移（ESIPT），一个新的设计概念，提供大的光谱位移适合定量发射率测量。拟议的研究填补了金属离子形态生物化学中的一个关键利基。目前，缺乏一种非侵入性的锌特异性荧光传感器是研究细胞内锌调控和运输的一个限制因素。