Homogeneous mono-(125)i-insulins. Preparation and characterization of mono-(125)i-(tyr a14)-and mono-(125)i-(tyr a19)-insulin

Mono-(125)I-(Tyr A19)-insulin (Mono*A19) was prepared by iodinating MC porcine insulin with (125)I in acid medium using iodate (as oxidizing agent), followed by anion-exchange chromatography. Mono-(125)I-(Tyr A14)-insulin (Mono*A14) was prepared by iodinating MC porcine insulin with (125)I, using H(...

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Published in:Diabetologia Vol. 19; no. 6; pp. 546 - 554
Main Authors: Jørgensen, K H, Larsen, U D
Format: Journal Article
Language:English
Published: Germany 1980
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Summary:Mono-(125)I-(Tyr A19)-insulin (Mono*A19) was prepared by iodinating MC porcine insulin with (125)I in acid medium using iodate (as oxidizing agent), followed by anion-exchange chromatography. Mono-(125)I-(Tyr A14)-insulin (Mono*A14) was prepared by iodinating MC porcine insulin with (125)I, using H(2)O(2)/lactoperoxidase at neutral pH, followed by anion-exchange chromatography. The specific radioactivities were in the ranges of 120-200 and 220-300 mCi/mg for Mono*A19 and Mono*A14, respectively. Analyses of the intramolecular distributions of (125)I demonstrated that the preparations were 97-98% radiochemically pure. In both preparations, 98-99% of the radioactivity was capable of binding to insulin antibodies for up to 6 months of storage of the tracers. The IRI concentration decreased with the duration of storage. The greatest observed fall in IRI concentration was 70%. The ime course could be explained by the assumption that the disintegration of a (125)I-nucleus destroys the immunoreactivity of the insulin molecule in which the decay occurs.
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ISSN:0012-186X
DOI:10.1007/BF00253183