| Literature DB >> 29116504 |
Julius Grzeschik1, Doreen Könning1, Steffen C Hinz1, Simon Krah1,2, Christian Schröter1,2, Martin Empting3, Harald Kolmar4, Stefan Zielonka5,6.
Abstract
Besides classical antibodies with the composition of heavy and light chains, sharks produce a unique heavy chain only isotype, termed Immunoglobulin New Antigen Receptor (IgNAR), in which antigen binding is solely mediated by a single domain, referred to as vNAR. Owing to their high affinity and specificity combined with their small size and high stability, vNAR domains emerged as promising target-binding scaffolds that can be tailor-made for biotechnological and biomedical applications. Herein, we describe protocols for the construction of semi-synthetic, CDR3-randomized vNAR libraries for the isolation of target-specific antibodies using yeast surface display or phage display as platform technology. Additionally, we provide information for affinity maturation of target-specific molecules through CDR1 diversification and sublibrary establishment.Entities:
Keywords: Affinity maturation; Antibody engineering; IgNAR; Library generation; Phage display; Protein engineering; Semi-synthetic antibody library; Shark; Single-domain antibody; Yeast surface display; vNAR
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Year: 2018 PMID: 29116504 DOI: 10.1007/978-1-4939-7447-4_8
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745