MRC Laboratory of Molecular Biology , Francis Crick Avenue, Cambridge CB2 0QH, United Kingdom.
Department of Medicine, Addenbrooke's Hospital, University of Cambridge , Cambridge CB2 2QQ, United Kingdom.
J Am Chem Soc. 2017 Apr 19;139(15):5338-5350. doi: 10.1021/jacs.6b12460. Epub 2017 Apr 4.
Formaldehyde (FA) is a reactive signaling molecule that is continuously produced through a number of central biological pathways spanning epigenetics to one-carbon metabolism. On the other hand, aberrant, elevated levels of FA are implicated in disease states ranging from asthma to neurodegenerative disorders. In this context, fluorescence-based probes for FA imaging are emerging as potentially powerful chemical tools to help disentangle the complexities of FA homeostasis and its physiological and pathological contributions. Currently available FA indicators require direct modification of the fluorophore backbone through complex synthetic considerations to enable FA detection, often limiting the generalization of designs to other fluorophore classes. To address this challenge, we now present the rational, iterative development of a general reaction-based trigger utilizing 2-aza-Cope reactivity for selective and sensitive detection of FA in living systems. Specifically, we developed a homoallylamine functionality that can undergo a subsequent self-immolative β-elimination, creating a FA-responsive trigger that is capable of masking a phenol on a fluorophore or any other potential chemical scaffold for related imaging and/or therapeutic applications. We demonstrate the utility of this trigger by creating a series of fluorescent probes for FA with excitation and emission wavelengths that span the UV to visible spectral regions through caging of a variety of dye units. In particular, Formaldehyde Probe 573 (FAP573), based on a resorufin scaffold, is the most red-shifted and FA sensitive in this series in terms of signal-to-noise responses and enables identification of alcohol dehydrogenase 5 (ADH5) as an enzyme that regulates FA metabolism in living cells. The results provide a starting point for the broader use of 2-aza-Cope reactivity for probing and manipulating FA biology.
甲醛(FA)是一种反应性信号分子,通过跨越表观遗传学到一碳代谢的许多中心生物途径不断产生。另一方面,异常升高的 FA 水平与从哮喘到神经退行性疾病的疾病状态有关。在这种情况下,用于 FA 成像的荧光探针作为潜在的强大化学工具出现,有助于理清 FA 动态平衡及其生理和病理贡献的复杂性。目前可用的 FA 指示剂需要通过复杂的合成考虑直接修饰荧光团骨架,以实现 FA 检测,这通常限制了设计在其他荧光团类别中的通用性。为了解决这个挑战,我们现在提出了一种基于合理的、迭代的 2-氮杂 Cope 反应的通用反应型触发的理性开发,用于在活系统中选择性和灵敏地检测 FA。具体来说,我们开发了一种同型烯丙胺官能团,它可以进行随后的自消去β-消除,产生一种对 FA 有反应的触发物,能够掩盖荧光团上的苯酚或任何其他潜在的化学支架,用于相关的成像和/或治疗应用。我们通过创建一系列用于 FA 的荧光探针来证明这种触发物的实用性,这些探针的激发和发射波长跨越 UV 至可见光谱区域,通过各种染料单元的笼蔽。特别是,基于 Resorufin 支架的甲醛探针 573(FAP573)在信号噪声响应方面是该系列中红移最大、对 FA 最敏感的,它能够识别出醇脱氢酶 5(ADH5)是一种在活细胞中调节 FA 代谢的酶。这些结果为更广泛地利用 2-氮杂 Cope 反应来探测和操纵 FA 生物学提供了一个起点。