| Literature DB >> 28255872 |
Xuelian Bai1, Hyunbo Shim2,3.
Abstract
Many large synthetic antibody libraries have been designed, constructed, and successfully generated high-quality antibodies suitable for various demanding applications. While synthetic antibody libraries have many advantages such as optimized framework sequences and a broader sequence landscape than natural antibodies, their sequence diversities typically are generated by random combinatorial synthetic processes which cause the incorporation of many undesired CDR sequences. Here, we describe the construction of a synthetic scFv library using oligonucleotide mixtures that contain predefined, non-combinatorially synthesized CDR sequences. Each CDR is first inserted to a master scFv framework sequence and the resulting single-CDR libraries are subjected to a round of proofread panning. The proofread CDR sequences are assembled to produce the final scFv library with six diversified CDRs.Entities:
Keywords: Antibody library; Non-combinatorial CDR diversity; Phage display; Synthetic CDR diversity; Synthetic antibody library; scFv
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Year: 2017 PMID: 28255872 DOI: 10.1007/978-1-4939-6857-2_2
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745