AI Article Synopsis

  • The introduction of unnatural amino acids (uAA) into proteins allows for unique functional groups to be added, which is valuable for research and protein engineering.
  • Incorporating uAAs can affect how well a protein is expressed and how it functions, but predicting these effects is still complicated and often requires extensive trial and error.
  • A new in vitro system was developed to quickly and efficiently screen multiple protein variants with uAAs, reducing the screening time from weeks to hours while providing valuable insights into the effects of uAAs on protein behavior.

Article Abstract

The incorporation of unnatural amino acids (uAA) can introduce novel functional groups into proteins site-specifically, with important applications in basic sciences and protein engineering. However, uAA incorporation can impact protein expression and functional activity depending on its location within the protein-a process that is not yet completely understood and difficult to predict. Therefore, practical applications often necessitate a time-consuming optimization of uAA location by individual gene cloning, expressions, purification, and evaluations for each location tested. To address this limitation, we introduce a streamlined and versatile in vitro system to rapidly express and screen uAA-containing proteins without cumbersome cell culturing or purification procedures. We utilized this technology to simultaneously screen 24 different t4-lysozyme mutants with different uAA incorporation sites in a matter of hours, compared to weeks-long workflow of conventional methods. Screening data offered a mechanistic explanation to some effects of uAA incorporation on expression and activity. Despite these insights, rational prediction of such effects remained challenging, further confirming the value of a rapid screening approach. Biotechnol. Bioeng. 2017;114: 2412-2417. © 2017 Wiley Periodicals, Inc.

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Source
http://dx.doi.org/10.1002/bit.26305DOI Listing

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