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Area of Science:

  • Biophotonics and Imaging
  • Fluorescent Probe Development
  • Spectroscopy and Computational Chemistry

Background:

  • Fluorescent probes with long emission wavelengths, high fluorescence quantum yields (FQYs), and large Stokes shifts are crucial for biological imaging.
  • Current fluorescent probe development is often inefficient and relies on trial-and-error.
  • Achieving far-red/near-infrared emission typically requires extended conjugation, often leading to reduced fluorescence.

Purpose of the Study:

  • To discuss an effective red-shifting strategy for fluorescent probes.
  • To present an alternative to conventional intramolecular charge transfer (ICT) strategies for achieving redder emission.
  • To explore advancements in noncanonical fluorescent protein design and generalization to other fluorophore scaffolds.

Main Methods:

  • A novel red-shifting strategy based on the green fluorescent protein chromophore.
  • Synergistic tuning of electronic ground and excited states.
  • Spectroscopy and computation-aided design principles.

Main Results:

  • The proposed strategy enables efficient red-shifting of emission wavelengths.
  • It preserves or enhances desirable properties like high fluorescence quantum yields (FQYs).
  • This approach offers a potentially shorter path to redder emission compared to ICT strategies.

Conclusions:

  • The discussed strategy provides an efficient route to develop advanced fluorescent probes.
  • This method can accelerate the design of noncanonical fluorescent proteins and other fluorophores.
  • It holds promise for creating superior probes for biological imaging with enhanced red/near-infrared emission.