| Literature DB >> 35727446 |
Lucy Green1, Nigel S Scrutton1, Andrew Currin2.
Abstract
Directed evolution is a powerful tool for the rapid improvement of a target protein toward a desired fitness criteria, such as activity, specificity, or stability. In order to achieve these desired improvements, it is often beneficial to subject the entirety of the protein to mutagenesis. However, the creation of such libraries by targeted methods (i.e. site-directed mutagenesis) can be a laborious and costly task. Here we outline the GeneORator method, which uses Boolean "OR" logic to introduce specific codon mutations at multiple loci in a single reaction, thereby greatly reducing the experimental workload. The method describes library synthesis using asymmetric PCR, in which mutagenic primers are designed to create OR-type mutations at multiple sites of variation in a two-step protocol. As an example, we show how this can be utilized for controlled and economical mutagenesis of every amino acid codon in a gene.Entities:
Keywords: Asymmetric PCR; DNA library assembly; Directed evolution; Synthetic biology; Variant libraries
Mesh:
Substances:
Year: 2022 PMID: 35727446 DOI: 10.1007/978-1-0716-2152-3_7
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745