| Literature DB >> 26945728 |
Michela Pasello1, Silvia Zamboni2, Alessandra Mallano3, Michela Flego3, Piero Picci4, Maurizio Cianfriglia3, Katia Scotlandi5.
Abstract
Human monoclonal antibodies are a powerful tool with increasingly successful exploitations and the single chain fragment variable format can be considered the building block for the implementation of more complex and effective antibody-based constructs. Phage display is one of the best and most efficient methods to isolate human antibodies selected from an efficient and variable phage display library. We report a method for the construction of a human naïve single-chain variable fragment library, termed IORISS1. Many different sets of oligonucleotide primers as well as optimized electroporation and ligation reactions were used to generate this library of 1.2×10(9) individual clones. The key difference is the diversity of variable gene templates, which was derived from only 15 non-immunized human donors. The method described here, was used to make a new human naïve single-chain fragment variable phage display library that represents a valuable source of diverse antibodies that can be used as research reagents or as a starting point for the development of therapeutics. Using biopanning, we determined the ability of IORISS1 to yield antibodies. The results we obtained suggest that, by using an optimized protocol, an efficient phage antibody library can be generated.Entities:
Keywords: Biopanning; IORISS1; Monoclonal antibody; Naïve library single-chain variable fragment; Phage display
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Year: 2016 PMID: 26945728 DOI: 10.1016/j.jbiotec.2016.02.034
Source DB: PubMed Journal: J Biotechnol ISSN: 0168-1656 Impact factor: 3.307