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Introduction of Plasmid Encoding for Rare tRNAs Reduces Amplification Bias in Phage Display Biopanning
Author(s) -
Benjamin J. Umlauf,
Michael J. McGuire,
Kathlynn C. Brown
Publication year - 2015
Publication title -
biotechniques
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.617
H-Index - 131
eISSN - 1940-9818
pISSN - 0736-6205
DOI - 10.2144/000114256
Subject(s) - biopanning , phage display , plasmid , escherichia coli , biology , genetics , codon usage bias , phagemid , directed evolution , selection (genetic algorithm) , computational biology , bacteriophage , peptide library , dna , gene , mutant , computer science , genome , artificial intelligence , antibody , peptide sequence
Amplification bias is a major hurdle in phage display protocols because it imparts additional, unintended selection pressure beyond binding to the desired target. One potential source of amplification bias is the inherent lack of codon optimization that occurs within phage display libraries. Here we present a method that reduces amplification bias by addition of a plasmid that encodes six low abundance tRNAs into K91 Escherichia coli. This new strain, termed K91+, is used to amplify phage during the selection process. We demonstrate the importance of rare codon usage in phage production, and our method produced an overall increase in uniformity of phage production in a random library. Both of these variables are improved in E. coli K91+ compared with the parental K91 strain. This simple solution, requiring only a commercially available plasmid and an additional antibiotic, can reduce amplification bias in phage display protocols.

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