Molecules 2014, 19(2), 2135-2165; doi:10.3390/molecules19022135
Review

Radiolabeling Strategies for Tumor-Targeting Proteinaceous Drugs

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Received: 6 September 2013; in revised form: 16 January 2014 / Accepted: 1 February 2014 / Published: 18 February 2014
(This article belongs to the Special Issue Reagents and Methods for Protein Target Identification)
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Abstract: Owing to their large size proteinaceous drugs offer higher operative information content compared to the small molecules that correspond to the traditional understanding of druglikeness. As a consequence these drugs allow developing patient-specific therapies that provide the means to go beyond the possibilities of current drug therapy. However, the efficacy of these strategies, in particular “personalized medicine”, depends on precise information about individual target expression rates. Molecular imaging combines non-invasive imaging methods with tools of molecular and cellular biology and thus bridges current knowledge to the clinical use. Moreover, nuclear medicine techniques provide therapeutic applications with tracers that behave like the diagnostic tracer. The advantages of radioiodination, still the most versatile radiolabeling strategy, and other labeled compounds comprising covalently attached radioisotopes are compared to the use of chelator-protein conjugates that are complexed with metallic radioisotopes. With the techniques using radioactive isotopes as a reporting unit or even the therapeutic principle, care has to be taken to avoid cleavage of the radionuclide from the protein it is linked to. The tracers used in molecular imaging require labeling techniques that provide site specific conjugation and metabolic stability. Appropriate choice of the radionuclide allows tailoring the properties of the labeled protein to the application required. Until the event of positron emission tomography the spectrum of nuclides used to visualize cellular and biochemical processes was largely restricted to iodine isotopes and 99m-technetium. Today, several nuclides such as 18-fluorine, 68-gallium and 86-yttrium have fundamentally extended the possibilities of tracer design and in turn caused the need for the development of chemical methods for their conjugation.
Keywords: radionuclides; radiometals; chelator; prosthetic groups; radiohalogenation; carrier molecules; proteins; radiopharmaceuticals; diagnostic imaging
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MDPI and ACS Style

Sugiura, G.; Kühn, H.; Sauter, M.; Haberkorn, U.; Mier, W. Radiolabeling Strategies for Tumor-Targeting Proteinaceous Drugs. Molecules 2014, 19, 2135-2165.

AMA Style

Sugiura G, Kühn H, Sauter M, Haberkorn U, Mier W. Radiolabeling Strategies for Tumor-Targeting Proteinaceous Drugs. Molecules. 2014; 19(2):2135-2165.

Chicago/Turabian Style

Sugiura, Grant; Kühn, Helen; Sauter, Max; Haberkorn, Uwe; Mier, Walter. 2014. "Radiolabeling Strategies for Tumor-Targeting Proteinaceous Drugs." Molecules 19, no. 2: 2135-2165.

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