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Enzymatic Formation of an Artificial Base Pair Using a Modified Purine Nucleoside Triphosphate
Author(s) -
Marie Flamme,
Pascal Röthlisberger,
Fabienne LeviAcobas,
Mohit Chawla,
Romina Oliva,
Luigi Cavallo,
Gilles Gasser,
Philippe Marlière,
Piet Herdewijn,
Marcel Hollenstein
Publication year - 2020
Publication title -
acs chemical biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.899
H-Index - 111
eISSN - 1554-8937
pISSN - 1554-8929
DOI - 10.1021/acschembio.0c00396
Subject(s) - base pair , nucleic acid , nucleotide , combinatorial chemistry , nucleoside , alphabet , synthetic biology , chemistry , purine , base (topology) , dna , stereochemistry , enzyme , computational biology , biology , biochemistry , gene , mathematics , mathematical analysis , linguistics , philosophy
The expansion of the genetic alphabet with additional, unnatural base pairs (UBPs) is an important and long-standing goal in synthetic biology. Nucleotides acting as ligands for the coordination of metal cations have advanced as promising candidates for such an expansion of the genetic alphabet. However, the inclusion of artificial metal base pairs in nucleic acids mainly relies on solid-phase synthesis approaches, and very little is known about polymerase-mediated synthesis. Herein, we report the selective and high yielding enzymatic construction of a silver-mediated base pair (dIm C -Ag I -dPur P ) as well as a two-step protocol for the synthesis of DNA duplexes containing such an artificial metal base pair. Guided by DFT calculations, we also shed light into the mechanism of formation of this artificial base pair as well as into the structural and energetic preferences. The enzymatic synthesis of the dIm C -Ag I -dPur P artificial metal base pair provides valuable insights for the design of future, more potent systems aiming at expanding the genetic alphabet.

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