Literature DB >> 16144377

Polymerase evolution: efforts toward expansion of the genetic code.

Aaron M Leconte1, Liangjing Chen, Floyd E Romesberg.   

Abstract

Genetic information is encoded by, but potentially not limited to, a four-letter alphabet. A variety of predominantly hydrophobic nucleobase analogues that form self-pairs in DNA have been examined as third base pair candidates. For example, the PICS self-pair is both stable in duplex DNA and synthesized by some wild-type polymerases with reasonable efficiency. These efforts to expand the genetic code are expected to be facilitated by optimizing both the unnatural nucleobase analogues and the polymerases that replicate them. Here, we report the use of an activity-based selection system to evolve a DNA polymerase that more efficiently replicates DNA containing the PICS self-pair. The selection system is based on the co-display on phage of DNA polymerase libraries and a DNA substrate containing the self-pair. Only polymerases that accept the unnatural substrate incorporate a biotin-dUTP to the attached primer and may then be isolated on a streptavidin solid support. A mutant of Sf polymerase, P2, was evolved which both inserts dPICSTP opposite dPICS in the template and extends the unnatural primer terminus by incorporation of the next correct natural dNTP, where the parental enzyme catalyzes neither step at detectable rates. P2 was found to be a triple mutant of Sf, with the mutations F598I, I614F, and Q489H. The evolved properties of P2, as well as the observed mutations, are consistent with an increased affinity for the DNA primer-template containing the self-pair.

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Year:  2005        PMID: 16144377      PMCID: PMC2538546          DOI: 10.1021/ja053322h

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  11 in total

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Journal:  Proc Natl Acad Sci U S A       Date:  2003-04-03       Impact factor: 11.205

3.  Determinants of unnatural nucleobase stability and polymerase recognition.

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4.  Minimal kinetic mechanism for misincorporation by DNA polymerase I (Klenow fragment).

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5.  Enzymatic incorporation of a new base pair into DNA and RNA extends the genetic alphabet.

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6.  An induced-fit kinetic mechanism for DNA replication fidelity: direct measurement by single-turnover kinetics.

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Journal:  Biochemistry       Date:  1991-01-15       Impact factor: 3.162

7.  Crystal structures of open and closed forms of binary and ternary complexes of the large fragment of Thermus aquaticus DNA polymerase I: structural basis for nucleotide incorporation.

Authors:  Y Li; S Korolev; G Waksman
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8.  Effect of reaction pH on the fidelity and processivity of exonuclease-deficient Klenow polymerase.

Authors:  K A Eckert; T A Kunkel
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9.  Efforts to expand the genetic alphabet: identification of a replicable unnatural DNA self-pair.

Authors:  Allison A Henry; Anne Goldbech Olsen; Shigeo Matsuda; Chengzhi Yu; Bernhard H Geierstanger; Floyd E Romesberg
Journal:  J Am Chem Soc       Date:  2004-06-09       Impact factor: 15.419

10.  Expanding the substrate repertoire of a DNA polymerase by directed evolution.

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Journal:  J Am Chem Soc       Date:  2004-02-18       Impact factor: 15.419

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  10 in total

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2.  Directed evolution of DNA polymerases for next-generation sequencing.

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Review 3.  Engineering Polymerases for New Functions.

Authors:  Timothy A Coulther; Hannah R Stern; Penny J Beuning
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5.  Evolving a polymerase for hydrophobic base analogues.

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6.  Optimization of an unnatural base pair toward natural-like replication.

Authors:  Young Jun Seo; Gil Tae Hwang; Phillip Ordoukhanian; Floyd E Romesberg
Journal:  J Am Chem Soc       Date:  2009-03-11       Impact factor: 15.419

7.  DNA sequencing using polymerase substrate-binding kinetics.

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Journal:  Nat Commun       Date:  2015-01-23       Impact factor: 14.919

Review 8.  DNA polymerases engineered by directed evolution to incorporate non-standard nucleotides.

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Review 9.  Exploring the Chemistry of Genetic Information Storage and Propagation through Polymerase Engineering.

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Review 10.  Modified Nucleoside Triphosphates for In-vitro Selection Techniques.

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  10 in total

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