Related Experiment Video
Updated: Sep 18, 2025

Automated Two-dimensional Spatiotemporal Analysis of Mobile Single-molecule FRET Probes
Published on: November 23, 2021
Recent progress of dual-responsive fluorescent probes for polarity and analytes
Junru He1, Xuwei Han2, Yongkang Yue2
1School of Chemistry and Chemical Engineering, Shanxi University, Taiyuan 030006, China.
Abstract:
Polarity, as an indicator of the cellular microenvironment, regulates cell functions in conjunction with bioactive molecules including proteins, ROS, RNS, RSS, etc. Their synergistic effect is closely linked to the emergence and advancement of atherosclerosis, diabetes, cancer and neurodegenerative diseases. Accordingly, monitoring the collaborative changes to polarity and related biomolecules in real time is important and illustrates their biological and pathological roles. Fluorescence imaging revealed substantial benefits and prospects for the identification of the micro-environment and analytes in organisms due to its high resolution, non-invasiveness, and real-time monitoring features. In this review, we summarized progress made in research on multifunctional fluorescent probes for the simultaneous tracking of polarity and analytes in the past five years. Our focus centered on the design approaches, spectral properties and biological utilization of current multifunctional fluorescent probes for detecting polarity and analytes, and we analyzed their limitations and prospects. We anticipate that this review will inspire a panoramic understanding of the relationship between polarity and various biologically active molecules, and promote the further design of new probes for a deeper illustration of invisible biomechanisms.
Related Concept Videos
Labeling DNA Probes
Radioisotopes, fluorophores, or small molecule binding partners like biotin or digoxigenin, are the most widely used reporter tags for labeling DNA probes. These labels can be attached to the probe DNA molecule via...
Protein Dynamics in Living Cells
Fluorescent recovery after photobleaching (FRAP) is a fluorescent-protein-based detection technique used to quantify protein movement rates within the cell. This method exposes a small portion of the cell to an intense laser beam. The laser beam causes permanent photobleaching of the fluorophore-tagged proteins in the exposed region. As the bleached...

