A P(V) platform for oligonucleotide synthesis

Author:

Huang Yazhong12ORCID,Knouse Kyle W.32ORCID,Qiu Shenjie24ORCID,Hao Wei3ORCID,Padial Natalia M.3ORCID,Vantourout Julien C.3ORCID,Zheng Bin24,Mercer Stephen E.12ORCID,Lopez-Ogalla Javier3ORCID,Narayan Rohan3,Olson Richard E.12,Blackmond Donna G.3,Eastgate Martin D.24ORCID,Schmidt Michael A.24ORCID,McDonald Ivar M.124ORCID,Baran Phil S.3ORCID

Affiliation:

1. Small Molecule Drug Discovery, Bristol Myers Squibb, Cambridge, MA 02142, USA.

2. Elsie Biotechnologies, San Diego, CA 92121, USA.

3. Department of Chemistry, The Scripps Research Institute, La Jolla, CA 92037, USA.

4. Chemical Process Development, Bristol Myers Squibb, New Brunswick, NJ 08903, USA.

Abstract

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

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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