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Nat Chem Biol DOI:10.1038/nchembio.1453

Negative selection and stringency modulation in phage-assisted continuous evolution.

Publication TypeJournal Article
Year of Publication2014
AuthorsCarlson, JC, Badran, AH, Guggiana-Nilo, DA, Liu, DR
JournalNat Chem Biol
Volume10
Issue3
Pages216-22
Date Published2014 Mar
ISSN1552-4469
KeywordsBacteriophages, Biological Evolution, DNA-Directed RNA Polymerases, Evolution, Molecular, Genetic Variation, Mutation, Promoter Regions, Genetic, Substrate Specificity, Viral Proteins
Abstract

Phage-assisted continuous evolution (PACE) uses a modified filamentous bacteriophage life cycle to substantially accelerate laboratory evolution experiments. In this work, we expand the scope and capabilities of the PACE method with two key advances that enable the evolution of biomolecules with radically altered or highly specific new activities. First, we implemented small molecule-controlled modulation of selection stringency that enables otherwise inaccessible activities to be evolved directly from inactive starting libraries through a period of evolutionary drift. Second, we developed a general negative selection that enables continuous counterselection against undesired activities. We integrated these developments to continuously evolve mutant T7 RNA polymerase enzymes with ∼10,000-fold altered, rather than merely broadened, substrate specificities during a single three-day PACE experiment. The evolved enzymes exhibit specificity for their target substrate that exceeds that of wild-type RNA polymerases for their cognate substrates while maintaining wild type-like levels of activity.

DOI10.1038/nchembio.1453
Pubmed

http://www.ncbi.nlm.nih.gov/pubmed/24487694?dopt=Abstract

Alternate JournalNat. Chem. Biol.
PubMed ID24487694
PubMed Central IDPMC3977541
Grant List / / Howard Hughes Medical Institute / United States