High-Density DNA Functionalization by a Combination of Cu-Catalyzed and Cu-Free Click Chemistry

被引:73
作者
Gutsmiedl, Katrin [1 ]
Fazio, Danila [1 ]
Carell, Thomas [1 ]
机构
[1] CiPS, Dept Chem, D-81377 Munich, Germany
关键词
click chemistry; DNA labeling; nitrite oxides; nucleotides; polymerase chain reaction; AZIDE-ALKYNE CYCLOADDITION; FREE TRIAZOLE FORMATION; COPPER-FREE; IN-VIVO; 1.3-DIPOLARE CYCLOADDITIONEN; 1,3-DIPOLAR CYCLOADDITIONS; NUCLEOSIDE TRIPHOSPHATES; PHOTOCLICK CHEMISTRY; NUCLEIC-ACID; SIDE-CHAINS;
D O I
10.1002/chem.201000363
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We report the regioselective Cu-free click modification of styrene functionalized DNA with nitrite oxides. A series of modified oligodeoxynucleotides (nine base pairs) was prepared with increasing styrene density. 1,3-Dipolar cycloaddition with nitrite oxides allows the high density functionalization of the styrene modified DNA directly on the DNA solid support and in solution. This click reaction proceeds smoothly even directly in the DNA synthesizer and gives exclusively 3,5-disubstituted isoxazolines. Additionally, PCR products (300 and 900 base pairs) were synthesized with a styrene triphosphate and KOD XL polymerase. The click reaction on the highly modified PCR fragments allows functionalization of hundreds of styrene units on these large DNA fragments simultaneously. Even sequential Cu-free and Cu-catalyzed click reaction of PCR amplicons containing styrene and alkyne carrying nucleobases was achieved. This new approach towards high-density functionalization of DNA is simple, modular, and efficient.
引用
收藏
页码:6877 / 6883
页数:7
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