Efficient method for site-specific 18F-labeling of biomolecules using the rapid condensation reaction between 2-cyanobenzothiazole and cysteine

Bioconjug Chem. 2012 Sep 19;23(9):1902-8. doi: 10.1021/bc300273m. Epub 2012 Aug 10.

Abstract

An efficient method based on a rapid condensation reaction between 2-cyanobenzothiazole (CBT) and cysteine has been developed for (18)F-labeling of N-terminal cysteine-bearing peptides and proteins. An (18)F-labeled dimeric cRGD ([(18)F]CBTRGD(2)) has been synthesized with an excellent radiochemical yield (92% based on radio-HPLC conversion, 80% decay-corrected, and isolated yield) and radiochemical purity (>99%) under mild conditions using (18)F-CBT, and shown good in vivo tumor targeting efficiency for PET imaging. The labeling strategy was also applied to the site-specific (18)F-labeling of a protein, Renilla lucifierase (RLuc8) with a cysteine residue at its N-terminus. The protein labeling was achieved with 12% of decay-corrected radiochemical yield and more than 99% radiochemical purity. This strategy should provide a general approach for efficient and site-specific (18)F-labeling of various peptides and proteins for in vivo molecular imaging applications.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Benzothiazoles / chemistry*
  • Chromatography, High Pressure Liquid
  • Cysteine / chemistry*
  • Dimerization
  • Fluorine Radioisotopes / chemistry*
  • Mice
  • Mice, Nude
  • Nitriles / chemistry*
  • Positron-Emission Tomography

Substances

  • 2-cyanobenzothiazole
  • Benzothiazoles
  • Fluorine Radioisotopes
  • Nitriles
  • Cysteine