| Literature DB >> 26608419 |
Rabab M Abou El-Magd1, Nicolas F Vozza2, Jack A Tuszynski3, David S Wishart4.
Abstract
Isolation of single chain antibody fragment (scFv) clones from naïve Tomlinson I+J phage display libraries that specifically bind a small biomarker molecule, L-Carnitine, was performed using iterative affinity selection procedures. L-Carnitine has been described as a conditionally essential nutrient for humans. Abnormally high concentrations of L-Carnitine in urine are related to many health disorders including diabetes mellitus type 2 and lung cancer. ELISA-based affinity characterization results indicate that selectants preferentially bind to L-Carnitine in the presence of key bioselecting component materials and closely related L-Carnitine derivatives. In addition, the affinity results were confirmed using biophysical fluorescence quenching for tyrosine residues in the V segment. Small-scale production of the soluble fragment yielded 1.3mg/L using immunopure-immobilized protein A affinity column. Circular Dichroism data revealed that the antibody fragment (Ab) represents a folded protein that mainly consists of β-sheets. These novel antibody fragments may find utility as molecular affinity interface receptors in various electrochemical biosensor platforms to provide specific L-Carnitine binding capability with potential applications in metabolomic devices for companion diagnostics and personalized medicine applications. It may also be used in any other biomedical application where detection of the L-Carnitine level is important.Entities:
Keywords: Circular Dichroism (CD); Enzyme-linked immunosorbent assay (ELISA); Fluorescence quenching assay; L-Carnitine; Phage display; Single chain antibody fragment (scFv)
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Year: 2015 PMID: 26608419 DOI: 10.1016/j.jim.2015.11.006
Source DB: PubMed Journal: J Immunol Methods ISSN: 0022-1759 Impact factor: 2.303