On the Enzymatic Formation of Metal Base Pairs with Thiolated and pKa-Perturbed Nucleotides

被引:15
作者
Levi-Acobas, Fabienne [1 ]
Rothlisberger, Pascal [1 ]
Sarac, Ivo [1 ]
Marliere, Philippe [2 ]
Herdewijn, Piet [3 ]
Hollenstein, Marcel [1 ]
机构
[1] Inst Pasteur, CNRS, Dept Struct Biol & Chem, Lab Bioorgan Chem Nucle Acids,UMR3523, 28 Rue Docteur Roux, F-75724 Paris 15, France
[2] Univ Paris Saclay, CNRS, iSSB, UEVE,Genopole, 5 Rue Henri Desbrueres, F-91030 Evry, France
[3] Katholieke Univ Leuven, Inst Med Res, Dept Med Chem, Herestr 49, B-3000 Leuven, Belgium
关键词
DNA synthesis; expanded genetic alphabet; metal base pairs; polymerases; thiolated nucleotides; GENETIC ALPHABET EXPANSION; SEMISYNTHETIC ORGANISM; POLYMERASE RECOGNITION; DNA-POLYMERASES; REPLICATION; APTAMERS; IONS; EVOLUTION; RNA; AMPLIFICATION;
D O I
10.1002/cbic.201900399
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The formation of artificial metal base pairs is an alluring and versatile method for the functionalization of nucleic acids. Access to DNA functionalized with metal base pairs is granted mainly by solid-phase synthesis. An alternative, yet underexplored method, envisions the installation of metal base pairs through the polymerization of modified nucleoside triphosphates. Herein, we have explored the possibility of using thiolated and pK(a)-perturbed nucleotides for the enzymatic construction of artificial metal base pairs. The thiolated nucleotides S2C, S6G, and S4T as well as the fluorinated analogue 5FU are readily incorporated opposite a templating S4T nucleotide through the guidance of metal cations. Multiple incorporation of the modified nucleotides along with polymerase bypass of the unnatural base pairs are also possible under certain conditions. The thiolated nucleotides S4T, S4T, S2C, and S6G were also shown to be compatible with the synthesis of modified, high molecular weight single-stranded (ss)DNA products through TdT-mediated tailing reactions. Thus, sulfur-substitution and pK(a) perturbation represent alternative strategies for the design of modified nucleotides compatible with the enzymatic construction of metal base pairs.
引用
收藏
页码:3032 / 3040
页数:9
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