Radionuclide molecular imaging using Affibody molecules

Curr Pharm Biotechnol. 2010 Sep 1;11(6):581-9. doi: 10.2174/138920110792246609.

Abstract

The current way to increase efficacy of cancer therapy is the use of molecular recognition of aberrantly expressed gene products for selective treatment. However, only a fraction of the patients have tumors with a particular molecular target. Radionuclide imaging of molecular targets might help to stratify patient for cancer treatment. Affibody molecules are scaffold proteins, which can be selected for high affinity recognition of proteinaceous molecular targets. The capacity to re-fold under physiological conditions allows labeling of Affibody molecules in a broad range of pH and temperatures with preserved binding properties. Peptide synthesis or introduction of a unique cysteine enables site-specific labeling of Affibody molecules, resulting in uniform conjugates with well-defined pharmacological characteristics. The small size (7 kDa) of Affibody molecules provides rapid extravasation, rapid tumor penetration, and rapid clearance of unbound tracer from healthy organs and tissues. In combination with sub-nanomolar affinity, this results in high contrast in vivo imaging a few hours after injection. Excellent targeting has been demonstrated in pre-clinical studies with HER2-targeting Affibody molecules labeled with (99m)Tc and (111)In for single photon computed tomography (SPECT), and (18)F, (64)Cu, (124)I and (68)Ga for positron emission tomography (PET). Pilot clinical data confirm the high potential of Affibody molecules.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Humans
  • Image Enhancement / methods
  • Isotope Labeling / methods
  • Molecular Imaging / methods*
  • Neoplasms / diagnostic imaging*
  • Positron-Emission Tomography / methods*
  • Radioisotopes*
  • Radiopharmaceuticals*
  • Recombinant Fusion Proteins*

Substances

  • Radioisotopes
  • Radiopharmaceuticals
  • Recombinant Fusion Proteins