Literature DB >> 28255872

Construction of a scFv Library with Synthetic, Non-combinatorial CDR Diversity.

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

Mesh:

Substances:

Year:  2017        PMID: 28255872     DOI: 10.1007/978-1-4939-6857-2_2

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  2 in total

1.  Rational library design by functional CDR resampling.

Authors:  Qi Zhao; Diane Buhr; Courtney Gunter; Jenny Frenette; Mary Ferguson; Eric Sanford; Erika Holland; Chitra Rajagopal; Melissa Batonick; Margaret M Kiss; Michael P Weiner
Journal:  N Biotechnol       Date:  2017-12-11       Impact factor: 5.079

Review 2.  Protein Engineering: Advances in Phage Display for Basic Science and Medical Research.

Authors:  Elena K Davydova
Journal:  Biochemistry (Mosc)       Date:  2022-01       Impact factor: 2.487

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.