UNA single stranded oligomers for therapeutics
This invention provides UNA single-stranded oligomers for therapeutics. The UNA oligomers can be composed of one or more 2′-3′-seco-nucleomonomers and one or more natural or non-natural nucleotide monomers. Embodiments include UNA oligomers with phosphorothioate or boranophosphate intermonomer linkages. The UNA oligomers can be used for therapeutics that target oligonucleotides, nucleic acids, or RNAs to reduce their activity.
1. An oligomer comprising one or more 2′-3′-seco-nucleomonomers and one or more natural or non-natural nucleotide monomers, wherein the oligomer is a single stranded RNA oligomer and the 2′-3′-seco-nucleomonomers are monomer D
wherein Base is a nucleobase.
2. The oligomer of claim 1 , wherein the oligomer is from 8 to 62 monomers in length.
3. The oligomer of claim 1 , comprising from one to five 2′-3′-seco-nucleomonomers.
4. The oligomer of claim 1 , wherein one or more of the nucleotide monomers is a 2′-O-alkyl-RNA nucleotide analogue.
5. The oligomer of claim 1 , wherein one or more of the monomers are linked by a phosphorothioate linkage or a boranophosphate linkage.
6. The oligomer of claim 1 , wherein the oligomer is from 14 to 26 monomers in length.
7. The oligomer of claim 1 , comprising a monomer nucleobase sequence that is complementary to a target nucleotide sequence.
8. The oligomer of claim 1 , wherein the oligomer has increased or prolonged stability towards enzymatic degradation in a cell as compared to an oligonucleotide having the same nucleobase sequence, wherein the oligonucleotide is composed of only natural RNA monomers.
9. The oligomer of claim 1 , wherein the oligomer comprises two, three, four, or five 2′-3′-seco-nucleomonomers.