Method for selective oligonucleotide modification
Method for producing a modified oligonucleotide, wherein at least one polymer, preferably polyalkylene oxide, and/or a compound is covalently bound to the 5′-end or the 3′-end of the oligonucleotide via native ligation forming a native ligation site, with the proviso that the polymer and/or the compound is not a protein or peptide, if only the 5′-end of the oligonucleotide is modified by binding of the polymer or compound via native ligation. The invention is further directed to a modified oligonucleotide obtainable by the inventive method as well as the use of such modified oligonucleotide for the preparation of a medicament for preventing and/or treating a tumor, formation of metastasis, an immune disease or disorder, a cardiovascular disease or disorder, and/or a viral disease or disorder.
1. A method for producing a modified oligonucleotide, wherein at least one polymer and/or a compound is covalently bound to the 5″-end or the 3″-end of the oligonucleotide via native ligation forming a native ligation site, with the proviso that the polymer and/or the compound is not a protein or peptide if only the 5″-end of the oligonucleotide is modified by binding of the polymer or compound via native ligation.
2. The method according to claim 1 , wherein a further polymer and/or compound is bound to the native ligation site and/or the 3″-end of the 5″-end native ligation modified oligonucleotide, or to the ligation site and/or the 5″-end of the 3″-end native ligation modified oligonucleotide.
3. The method according to claim 1 ,
wherein the 5″-end or the 3″-end of the oligonucleotide is bound to a polymer and/or a compound via native ligation in a first step, the free 3″-end or the free 5″-end of the oligonucleotide is bound to a polymer and/or a compound in a second step, and the native ligation site is optionally bound to a polymer and/or a compound in a third step, or
wherein the 5″-end or the 3″-end of the oligonucleotide is bound to a polymer and/or a compound via native ligation in a first step, the native ligation site is bound to a polymer and/or a compound in a second step and the free 3″-end or the free 5″-end of the oligonucleotide is optionally bound to a polymer and/or a compound in a third step, or
wherein the 3″-end or the 5″-end of the oligonucleotide is bound to a polymer and/or a compound in a first step, the free 5″-end or the free 3″-end of the oligonucleotide is bound to a polymer and/or a compound via native ligation in a second step, and the ligation site is optionally bound to a polymer and/or a compound in a third step.
4. The method according to claim 1 , wherein the modified oligonucleotide is a TGF-β2, TGF-β1, TGF-β3, VEGF, IL-10, c-jun, c-fos, c-erbb2 (Her-2), or MIA antisense oligonucleotide and/or an antisense oligonucleotide hybridizing with one or more of the receptors of TGF-β2, TGF-β1, TGF-β3, VEGF, IL-10, c-jun, c-fos, c-erbb2 (Her-2), or MIA.
5. The method according to claim 1 , wherein the polymer is polyethylene glycol.
6. The method according to claim 1 , wherein the compound is a small molecule, an antibody, an antigen, an enzyme, a part of an antibody, an enzyme, or any peptide.
7. The method according to claim 1 , wherein the polymer and/or compound is bound to the oligonucleotide, with or without a linker.
8. The method according to claim 7 , wherein the linker is a reversible or irreversible linker.
9. The method according to claim 1 , wherein the modified oligonucleotide is bound to a solid support via the 5″- and/or 3″-end of the oligonucleotide and/or the ligation site.
10. The method according to claim 1 , wherein the polymer is polyethylene glycol selected from PEG-400, PEG-1000, PEG-2000, PEG-5000, or PEG10000.
11. The method according to claim 1 , wherein the compound is selected from an internalizing peptide, an aptamer, a spiegelmer, RNAi, shRNA, miRNA, a chromophor, a marker, biotin, a hormone, a signal peptide, a lipid, a fatty acid, a sugar, an amino acid, a receptor, a part of a receptor, or a ligand of a receptor or binding molecule.