Počet záznamů: 1  

Recombinant fragment of an antibody tailored for direct radioiodination

  1. 1. 0378891 - UMG-J 2013 RIV GB eng J - Článek v odborném periodiku
    Sedláček, Juraj - Fábry, Milan - Sieglová, Irena - Král, Vlastimil - Uhnáková, Bronislava - Mudra, M. - Kronrád, L. - Sawicka, A. - Mikolajczak, R. - Řezáčová, Pavlína
    Recombinant fragment of an antibody tailored for direct radioiodination.
    Journal of Labelled Compounds and Radiopharmaceuticals. Roč. 55, č. 1 (2012), s. 52-56. ISSN 0362-4803
    Grant CEP: GA MPO 2A-2TP1/076; GA MŠk 1M0505
    Výzkumný záměr: CEZ:AV0Z50520514
    Klíčová slova: I125 labelling * single-chain antibody variable fragment * tyrosine-rich polypeptide segment * fusion protein
    Kód oboru RIV: EB - Genetika a molekulární biologie
    Impakt faktor: 1.240, rok: 2012

    High specific radioactivity (per mass or per mole) is an important and desirable parameter for the radiopharmaceuticals that are intended to target disease biomarker molecules. In direct radioiodination of immunoglobulins or their fragments, the predominant chemical reaction is usually the monoiodination of the phenol rings of tyrosine amino acid residues. For such radioiodination, the maximum achievable level of labeling of a given protein molecule obviously correlates to the number of solvent-accessible tyrosine residues. The grafting of proteins with additional iodine-acceptor tyrosine residues by conventional chemical techniques has been recently reported. We show here that a recombinant single chain variable fragment (scFv) of an anti-b-III-tubulin antibody, having a potential use in imaging neural lesions or astrocytoma and certain nonneuronal tumors, can be modified in a similar manner. However, in contrast to previously published examples, tyrosine residues are added to the polypeptide main chain without any chemical reaction, solely with molecular cloning and recombinant expression. Importantly, the tailoring outlined here is carried out ‘once and for all’ at laboratory scale (modifying permanently the expressed nucleic acid), whereas chemical indirect methods are necessarily carried out either at production scale or always before each round of radioiodination.
    Trvalý link: http://hdl.handle.net/11104/0218862