| Literature DB >> 27156812 |
Shima Moradi-Kalbolandi1, Mahdi Habibi-Anbouhi2, Majid Golkar3, Mahdi Behdani4, Gashin Rezaei1, Leila Ghazizadeh1, Mohsen Abolhassani5, Mohammad Ali Shokrgozar6.
Abstract
Antibody engineering involves a range of custom modifications of immunoglobulins to improve their affinity, valency, and pharmacokinetics, ensuring a better target therapy achievement. A number of therapeutic antibodies have been used for cell surface receptor blockage, interfering with the ligand binding and inhibiting receptor-driven activation of cells. Here we describe the construction and characterization of a recombinant bivalent single-chain Fv (biscFv) that targets CD123. On conversion of anti-CD123 scFv to biscFv format, the recognition of the cognate ligand is not altered. Moreover, the increased overall efficacy of the anti-CD123 biscFv in binding and inhibition of CD123/IL-3 (interleukin-3) interactions in TF-1 cells is demonstrated.Entities:
Keywords: AML; Antibody engineering; Bivalent scFv (biscFv); CD123; Leukemic cancer stem cells
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Year: 2016 PMID: 27156812 DOI: 10.1016/j.ab.2016.04.017
Source DB: PubMed Journal: Anal Biochem ISSN: 0003-2697 Impact factor: 3.365