Literature DB >> 15994074

Semi-rational approaches to engineering enzyme activity: combining the benefits of directed evolution and rational design.

Roberto A Chica1, Nicolas Doucet, Joelle N Pelletier.   

Abstract

Many research groups successfully rely on whole-gene random mutagenesis and recombination approaches for the directed evolution of enzymes. Recent advances in enzyme engineering have used a combination of these random methods of directed evolution with elements of rational enzyme modification to successfully by-pass certain limitations of both directed evolution and rational design. Semi-rational approaches that target multiple, specific residues to mutate on the basis of prior structural or functional knowledge create 'smart' libraries that are more likely to yield positive results. Efficient sampling of mutations likely to affect enzyme function has been conducted both experimentally and, on a much greater scale, computationally, with remarkable improvements in substrate selectivity and specificity and in the de novo design of enzyme activities within scaffolds of known structure.

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Year:  2005        PMID: 15994074     DOI: 10.1016/j.copbio.2005.06.004

Source DB:  PubMed          Journal:  Curr Opin Biotechnol        ISSN: 0958-1669            Impact factor:   9.740


  69 in total

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Journal:  Proc Natl Acad Sci U S A       Date:  2010-11-02       Impact factor: 11.205

3.  Generation of longer emission wavelength red fluorescent proteins using computationally designed libraries.

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Journal:  Protein Sci       Date:  2007-11       Impact factor: 6.725

Review 5.  Progress in computational protein design.

Authors:  Shaun M Lippow; Bruce Tidor
Journal:  Curr Opin Biotechnol       Date:  2007-07-20       Impact factor: 9.740

6.  Computational structure-based redesign of enzyme activity.

Authors:  Cheng-Yu Chen; Ivelin Georgiev; Amy C Anderson; Bruce R Donald
Journal:  Proc Natl Acad Sci U S A       Date:  2009-02-19       Impact factor: 11.205

Review 7.  Directed evolution drives the next generation of biocatalysts.

Authors:  Nicholas J Turner
Journal:  Nat Chem Biol       Date:  2009-08       Impact factor: 15.040

8.  Optimizing glycosyltransferase specificity via "hot spot" saturation mutagenesis presents a catalyst for novobiocin glycorandomization.

Authors:  Gavin J Williams; Randal D Goff; Changsheng Zhang; Jon S Thorson
Journal:  Chem Biol       Date:  2008-04

9.  High tolerance to simultaneous active-site mutations in TEM-1 beta-lactamase: Distinct mutational paths provide more generalized beta-lactam recognition.

Authors:  Pierre-Yves De Wals; Nicolas Doucet; Joelle N Pelletier
Journal:  Protein Sci       Date:  2009-01       Impact factor: 6.725

10.  Combinatorial active-site variants confer sustained clavulanate resistance in BlaC β-lactamase from Mycobacterium tuberculosis.

Authors:  Philippe Egesborg; Hélène Carlettini; Jordan P Volpato; Nicolas Doucet
Journal:  Protein Sci       Date:  2014-12-30       Impact factor: 6.725

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