Han Hua, Han Bin, Peng Yongjin, Liu Yuling
3rd Affiliated Hospital of Jinzhou Medical University, Jinzhou, China.
Department of Physics, Tianjin Renai College, Tianjin, China.
Front Chem. 2025 Jul 23;13:1642191. doi: 10.3389/fchem.2025.1642191. eCollection 2025.
This study focuses on a multifunctional fluorescence probe JFT based on the FRET (Fluorescence Resonance Energy Transfer) and TICT (Twisted Intramolecular Charge Transfer) mechanism. JFT combines an electron donor and an acceptor, enabling it to detect sulfite and monitor intracellular viscosity. When reacting with sulfite, its electronic structure changes, turning off FRET and altering fluorescence wavelength and intensity. In different viscosity environments, the rotation of carbon-carbon bonds in the electron acceptor structure of JFT varies, affecting non-radiative transition pathways and fluorescence intensity. Theoretical calculations based on TDDFT reveal the electron distribution changes before and after the reaction with sulfite species, consistent with experimental phenomena. These findings deepen the understanding of the FRET mechanism of fluorescence probes and offer theoretical guidance for the design of more efficient fluorescence probes.
本研究聚焦于一种基于荧光共振能量转移(FRET)和扭曲分子内电荷转移(TICT)机制的多功能荧光探针JFT。JFT结合了电子供体和受体,使其能够检测亚硫酸盐并监测细胞内粘度。当与亚硫酸盐反应时,其电子结构发生变化,关闭FRET并改变荧光波长和强度。在不同的粘度环境中,JFT电子受体结构中碳 - 碳键的旋转会发生变化,影响非辐射跃迁途径和荧光强度。基于含时密度泛函理论(TDDFT)的理论计算揭示了与亚硫酸盐物种反应前后的电子分布变化,与实验现象一致。这些发现加深了对荧光探针FRET机制的理解,并为设计更高效的荧光探针提供了理论指导。