Site-Specific Labeling of Proteins with Near-IR Heptamethine Cyanine Dyes

Molecules. 2018 Nov 7;23(11):2900. doi: 10.3390/molecules23112900.

Abstract

Convenient labeling of proteins is important for observing its function under physiological conditions. In tissues particularly, heptamethine cyanine dyes (Cy-7) are valuable because they absorb in the near-infrared (NIR) region (750⁻900 nm) where light penetration is maximal. In this work, we found Cy-7 dyes with a meso-Cl functionality covalently binding to proteins with free Cys residues under physiological conditions (aqueous environments, at near neutral pH, and 37 °C). It transpired that the meso-Cl of the dye was displaced by free thiols in protein, while nucleophilic side-chains from amino acids like Tyr, Lys, and Ser did not react. This finding shows a new possibility for convenient and selective labeling of proteins with NIR fluorescent probes.

Keywords: cancer targeting; heptamethine cyanine; protein labeling; thiol labeling; vimentin.

MeSH terms

  • Amino Acids / chemistry
  • Carbocyanines / chemistry*
  • Fluorescent Dyes / chemistry*
  • Molecular Structure
  • Proteins / chemistry*
  • Spectroscopy, Near-Infrared*
  • Staining and Labeling*
  • Sulfhydryl Compounds

Substances

  • Amino Acids
  • Carbocyanines
  • Fluorescent Dyes
  • Proteins
  • Sulfhydryl Compounds