Radiolabelling of isopeptide N-epsilon-(gamma-glutamyl)-L-lysine by conjugation with N-succinimidyl-4-[F-18]fluorobenzoate

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • F Wüst - (Author)
  • C Hultsch - (Author)
  • R Bergmann - (Author)
  • B Johannsen - (Author)
  • T Henle - , Chair of Food Chemistry (Author)
  • Helmholtz-Zentrum Dresden-Rossendorf

Abstract

The isopeptide N-epsilon-(gamma-glutamyl)-L-lysine 4 was labelled with F-18 via N-succinimidyl-4-[F-18]fluorobenzoate ([F-18]SFB). A modified approach for the convenient synthesis of [F-18]SFB was used, and [F-18]SFB could be obtained in decay-corrected radiochemical yields of 44-53% (n=20) and radiochemical purity >95% within 40 min after EOB. For labelling N-epsilon-(gamma-glutamyl)-L-lysine with [F-18]SFB the effects of isopeptide concentration, temperature, and pH were studied to determine the optimum reaction conditions. The coupling reaction was shown to be temperature and pH independent while being strongly affected by the isopeptide concentration. Using the optimized labelling conditions, in a typical experiment 1.3 GBq of [F-18]SFB could be converted into 447MBq (46%, decay-corrected) of [F-18]fluorobenzoylated isopeptide within 45 min, including HPLC purification. (C) 2003 Elsevier Ltd. All rights reserved.

Details

Original languageEnglish
Pages (from-to)43-48
Number of pages6
JournalApplied radiation and isotopes
Volume59
Issue number1
Publication statusPublished - Jul 2003
Peer-reviewedYes

External IDs

Scopus 0142058825

Keywords

Keywords

  • F-18-labelling, positron emission tomography, isopeptide, [F-18]SFB, MICROBIAL TRANSGLUTAMINASE, PROTEINS, BIODISTRIBUTION, PEPTIDES, ACID