Synthesis and characterization of 18F-interleukin-8 using a cell-free translation system and 4-18F-fluoro-L-proline

Ryuichi Harada, Shozo Furumoto, Takeo Yoshikawa, Yoichi Ishikawa, Katsuhiko Shibuya, Nobuyuki Okamura, Kiichi Ishiwata, Ren Iwata, Kazuhiko Yanai

Research output: Contribution to journalArticlepeer-review

6 Citations (Scopus)


Macromolecules such as proteins are attracting increasing interest for molecular imaging. We previously proposed a novel strategy for preparing macromolecules labeled with a PET radionuclide, 11C, using a cell-free translation system with 11C-methionine. However, macromolecules tend to exhibit slower kinetics, thus requiring a longer scanning time. Here, we expand our strategy using 18F, which has a longer half-life, with the cell-free translation system with 4-18F-fluoro-L-proline (18F-FPro). We evaluated 18F-interleukin-8 (18F-IL-8) produced by this method in vitro and in vivo to provide a proof of concept of our strategy. Methods: We tested some fluorinated amino acids to be incorporated into a protein. Trans-18F-FPro was radiolabeled from the corresponding precursor. 18F-IL-8 was produced using the cell-free translation system with trans-18F-FPro instead of natural L-proline with incubation at 37°C for 120 min. An in vitro binding assay of 18F-IL-8 was performed using IL-8 receptor-expressing cells. After intravenous administration of 18FIL- 8, in vivo PET imaging of IL-8 receptor-expressing xenograft-bearing mice was performed using a small-animal PET system. Results: FPro was identified as an amino acid incorporated into the protein. 18F-IL-8 was successfully prepared using the cell-free translation system and trans-18F-FPro with the radiochemical yield of 1.5% (decay-corrected) based on trans-18F-FPro. In vitro binding assays of 18F-IL-8 demonstrated its binding to IL-8 receptor. In vivo PET imaging demonstrated that 18F-IL-8 clearly accumulated in IL-8 receptor-expressing xenografts in mice, unlike trans-18F-FPro. Conclusion: 18F-IL-8 produced by this method binds to IL-8 receptors in vitro, and 18F-IL-8 PET clearly visualizes its target receptor-expressing xenograft in vivo. Therefore, this technique might be useful for labeling macromolecules and performing preclinical evaluations of proteins of interest in vitro and in vivo.

Original languageEnglish
Pages (from-to)634-639
Number of pages6
JournalJournal of Nuclear Medicine
Issue number4
Publication statusPublished - 2016 Apr 1


  • Cell-free protein synthesis
  • F
  • Interleukin-8
  • Non-natural amino acid
  • PET

ASJC Scopus subject areas

  • Radiology Nuclear Medicine and imaging


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