125I-Tetrazines and Inverse-Electron-Demand Diels–Alder Chemistry: A Convenient Radioiodination Strategy for Biomolecule Labeling, Screening, and Biodistribution Studies Academic Article uri icon

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abstract

  • A convenient method to prepare radioiodinated tetrazines was developed, such that a bioorthogonal inverse electron demand Diels-Alder reaction can be used to label biomolecules with iodine-125 for in vitro screening and in vivo biodistribution studies. The tetrazine was prepared by employing a high-yielding oxidative halo destannylation reaction that concomitantly oxidized the dihydrotetrazine precursor. The product reacts quickly and efficiently with trans-cyclooctene derivatives. Utility was demonstrated through antibody and hormone labeling experiments and by evaluating products using standard analytical methods, in vitro assays, and quantitative biodistribution studies where the latter was performed in direct comparison to Bolton-Hunter and direct iodination methods. The approach described provides a convenient and advantageous alternative to conventional protein iodination methods that can expedite preclinical development and evaluation of biotherapeutics.

authors

  • Albu, Silvia A
  • Al-Karmi, Salma A
  • Vito, Alyssa
  • Dzandzi, James PK
  • Zlitni, Aimen
  • Beckford-Vera, Denis
  • Blacker, Megan
  • Janzen, Nancy
  • Patel, Ramesh M
  • Capretta, Alfredo
  • Valliant, John F

publication date

  • January 20, 2016

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