A P(V) platform for oligonucleotide synthesis
Author(s) -
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
Publication year - 2021
Publication title -
science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.abi9727
Subject(s) - phosphodiester bond , oligonucleotide , flexibility (engineering) , combinatorial chemistry , computer science , computational biology , dna , chemistry , sequence (biology) , nanotechnology , biology , biochemistry , materials science , mathematics , rna , statistics , gene
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, Huanget 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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