García Santiago, Carmona-Santiago Gustavo, Jiménez-Sánchez Arturo
Instituto de Química, Universidad Nacional Autónoma de México, Ciudad Universitaria, Circuito Exterior s/n, Coyoacán, Ciudad de México 04510, México.
Anal Chem. 2024 Dec 10;96(49):19183-19189. doi: 10.1021/acs.analchem.4c05022. Epub 2024 Nov 22.
The development of small-molecule fluorescent probes has revolutionized the monitoring of physicochemical parameters, offering unprecedented insights into biological processes. In this perspective, we critically examine recent advances and trends in the design and application of fluorescent probes for real-time monitoring of subcellular environments. Traditional concepts such as membrane potential, microviscosity, and micropolarity have been superseded by more biologically relevant parameters like membrane voltage, tension, and hydration, enhancing the accuracy of physiological assessments. This redefinition not only presents an evolved concept with broader applications in monitoring subcellular dynamics but also addresses the unmet needs of subcellular biology more effectively. We also highlight the limitations of commonly used probes in providing specific information about the redox environment, noting their nonspecificity to oxidants and the influence of various chemical interactions. These probes typically rely on free radical mechanisms and require metal catalysts to react with hydrogen peroxide. They include naphthalimide, fluorescein, BODIPY, rhodamine, cyanine cores to cover the UV-vis-near-infrared window. The motif of this perspective is to provide critical insights into trending fluorescent-based systems employed in real-time or physicochemical-responsive monitoring, thus aiming to inform and inspire further research in creating robust and efficient fluorescent probes for comprehensive monitoring applications.
小分子荧光探针的发展彻底改变了对物理化学参数的监测,为生物过程提供了前所未有的见解。从这个角度来看,我们批判性地审视了用于实时监测亚细胞环境的荧光探针在设计和应用方面的最新进展和趋势。诸如膜电位、微粘度和微极性等传统概念已被膜电压、张力和水合作用等更具生物学相关性的参数所取代,提高了生理评估的准确性。这种重新定义不仅提出了一个在监测亚细胞动态方面具有更广泛应用的进化概念,而且更有效地满足了亚细胞生物学未满足的需求。我们还强调了常用探针在提供有关氧化还原环境的特定信息方面的局限性,指出它们对氧化剂的非特异性以及各种化学相互作用的影响。这些探针通常依赖自由基机制,并且需要金属催化剂与过氧化氢反应。它们包括萘酰亚胺、荧光素、BODIPY、罗丹明、花菁核心,以覆盖紫外 - 可见 - 近红外窗口。本文的主旨是对用于实时或物理化学响应监测的基于荧光的系统提供批判性见解,从而旨在为创建用于全面监测应用的强大而高效的荧光探针提供信息并激发进一步的研究。