磷酸二酯键
寡核苷酸
化学
灵活性(工程)
DNA
序列(生物学)
计算机科学
计算生物学
组合化学
核糖核酸
生物化学
纳米技术
生物
材料科学
数学
统计
基因
作者
Yazhong Huang,Kyle W. Knouse,Shenjie Qiu,Wei Hao,Natalia M. Padial,Julien C. Vantourout,Bin Zheng,Stephen E. Mercer,Javier López-Ogalla,Rohan Narayan,Richard E. Olson,Donna G. Blackmond,Martin D. Eastgate,Michael A. Schmidt,Ivar M. McDonald,Phil S. Baran
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2021-09-09
卷期号:373 (6560): 1265-1270
被引量:52
标识
DOI:10.1126/science.abi9727
摘要
Platform for the synthesis of diverse oligos DNA is primarily viewed as a carrier of information encoded in the sequence of bases, but the chemistry of the phosphodiester backbone is crucial to oligonucleotide stability and structure. Building on previous work in synthetic P(V) phosphorothioate coupling chemistry, Huang et al . developed two new reagents for making phosphorodithioate- and phosphate-based linkages (see the Perspective by Virta). The authors incorporated all of these reagents into a unified P(V)-based synthesis platform capable of running at high efficiency on a commercial automated solid-phase synthesizer. They demonstrate the flexibility of this system by producing oligonucleotides with all three linkage types in specific positions. Access to such precisely constructed molecules opens new approaches to therapeutic oligonucleotide design. —MAF
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