An Efficient and Modular Route to Sequence- Defined Polymers Appended to DNA

被引:118
作者
Edwardson, Thomas G. W. [1 ]
Carneiro, Karina M. M. [1 ]
Serpell, Christopher J. [1 ]
Sleiman, Hanadi F. [1 ]
机构
[1] McGill Univ, Dept Chem, Montreal, PQ H3A 0B8, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
amphiphiles; DNA; polymers; self-assembly; solid-phase synthesis; SYNTHETIC-POLYMERS; PEPTIDE-SYNTHESIS;
D O I
10.1002/anie.201310937
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Inspired by biological polymers, sequence-controlled synthetic polymers are highly promising materials that integrate the robustness of synthetic systems with the information-derived activity of biological counterparts. Polymer-biopolymer conjugates are often targeted to achieve this union; however, their synthesis remains challenging. We report a stepwise solid-phase approach for the generation of completely monodisperse and sequence-defined DNA-polymer conjugates using readily available reagents. These polymeric modifications to DNA display self-assembly and encapsulation behavioras evidenced by HPLC, dynamic light scattering, and fluorescence studieswhich is highly dependent on sequence order. The method is general and has the potential to make DNA-polymer conjugates and sequence-defined polymers widely available.
引用
收藏
页码:4567 / 4571
页数:5
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