A New Strategy for the Preparation of Peptide-Targeted Radiopharmaceuticals Based on an Fmoc-Lysine-Derived Single Amino Acid Chelate (SAAC). Automated Solid-Phase Synthesis, NMR Characterization, and in Vitro Screening of fMLF(SAAC)G and fMLF[(SAAC-Re(CO)3)+]G

Karin A. Stephenson, Jon A Zubieta, Sangeeta Ray Banerjee, Murali K. Levadala, Linda Taggart, Loma Ryan, Nicole McFarlane, Douglas R. Boreham, Kevin P. Maresca, John W. Babich, John F. Valliant

Research output: Contribution to journalArticle

103 Scopus citations


A tridentate single amino acid chelate (SAAC) derived from N- α-Fmoc-L-lysine was incorporated within a short peptide sequence using an automated peptide synthesizer. Novel derivatives of the chemotactic peptide fMLF were prepared such that the SAAC and its Re complex were selectively placed between a terminal glycine amino acid and the targeting fMLF sequence. The products, which were synthesized in parallel, were characterized by mass spectrometry and multi-NMR spectroscopy. The latter technique demonstrated that the structures of the targeting portions of the peptides are the same in the SAAC and Re-SAAC derivatives. The affinities of the reported compounds for the formyl peptide receptor were subsequently determined using flow cytometry and were found to be comparable to that of the parent peptide. The results of this work demonstrate the feasibility and numerous benefits of using the SAAC system to prepare peptide-targeted Tc(I) and Re(I) radiopharmaceuticals.

Original languageEnglish (US)
Pages (from-to)128-136
Number of pages9
JournalBioconjugate Chemistry
Issue number1
StatePublished - Jan 2004


ASJC Scopus subject areas

  • Chemistry(all)
  • Organic Chemistry
  • Clinical Biochemistry
  • Biochemistry, Genetics and Molecular Biology(all)
  • Biochemistry

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