Cloning of Affibody Libraries for Display Methods

• Published in: Cold Spring Harbor protocols Vol. 2024; no. 11; p. pdb.prot108398
• Main Authors: Ståhl, Stefan, Hjelm, Linnea Charlotta, Dahlsson Leitao, Charles, Löfblom, John, Lindberg, Hanna
• Format: Journal Article
• Language: English
• Published: United States 01.11.2024
• Subjects: Cell Surface Display Techniques - methods; Cloning, Molecular - methods; Escherichia coli - genetics; Gene Library; Peptide Library; Polymerase Chain Reaction - methods; Recombinant Fusion Proteins - genetics; Staphylococcus - genetics
• ISSN: 1559-6095
• DOI: 10.1101/pdb.prot108398

Affibody molecules are small (6-kDa) affinity proteins folded in a three-helical bundle and generated by directed evolution for specific binding to various target molecules. The most advanced affibody molecules are currently tested in the clinic, and data from more than 300 subjects show excellent activity and safety profiles. The generation of affibody molecules against a particular target starts with the generation of an affibody library, which can then be used for panning using multiple methods and selection systems. This protocol describes the molecular cloning of DNA-encoded affibody libraries to a display vector of choice, for either phage, , or display. The DNA library can come from different sources, such as error-prone polymerase chain reaction (PCR), molecular shuffling of mutations from previous selections, or, more commonly, from DNA synthesis using various methods. Restriction enzyme-based subcloning is the most common strategy for affibody libraries of higher diversity (e.g., >10 variants) and is described here.