Anandamide-modified nucleic acid molecules
The present invention refers to a conjugate comprising at least one polyunsaturated fatty acid residue, particularly an arachidonic acid residue, more particularly an anandamide (arachidonoyl ethanol amide) residue and covalently bound thereto at least one nucleosidic component selected from nucleic acids, nucleosides and nucleotides. This conjugate is suitable for the transfection of cells such as mammalian cells including human cells with high efficacy. Thus, a new delivery vehicle for therapeutic molecules including antisense molecules, siRNA molecules, miRNA molecules, antagomirs or precursors of such molecules, as well as the therapeutic nucleosides or nucleotides, is provided.
1. A conjugate comprising at least one arachidonic acid residue and covalently bound thereto at least one nucleosidic component selected from nucleic acids, nucleosides and nucleotides.
2. The conjugate of claim 1 having the general formula (Ia) or (Ib)
F n -(L m -N) r (Ia)
F n -(L m -N) r -L m -F n (Ib)
wherein
F is an arachidonic acid residue,
L is a linker,
N is a nucleosidic component selected from nucleic acids, nucleosides and nucleotides,
n is an integer from 1-10,
m is 0 or 1,
r is an integer from 1-25.
3. The conjugate of claim 1 comprising a further ligand covalently bound to the at least one nucleosidic component.
4. The conjugate of claim 3 having the general formula (II)
F n -(L m -N)r-L m -Z s (II)
wherein
F is an arachidonic acid residue,
L is a linker,
n is an integer from 1-10,
m is 0 or 1,
N is a nucleosidic component selected from nucleic acids, nucleosides and nucleotides,
r is an integer from 1-25,
Z is a further receptor ligand, and
s is an integer from 1-10.
5. The conjugate of claim 1 , wherein the arachidonic acid residue is selected from the residue of a free arachidonic acid, an arachidonic acid ester or an arachidonic acid amide, an arachidonic acid sulfonate, an arachidonic acid sulfate, an arachidonic acid phosphonate or an arachidonic acid phosphate.
6. The conjugate of claim 1 , wherein the arachidonic acid residue is covalently bound to the at least one nucleosidic component via a linker.
7. The conjugate of claim 6 , wherein the linker comprises a cyclic group formed by a Click reaction.
8. The conjugate of claim 1 , wherein the nucleosidic component is a nucleic acid molecule.
9. The conjugate of claim 1 , wherein the nucleosidic component is a nucleic acid molecule comprising at least one modified building block.
10. The conjugate of claim 1 , wherein the nucleosidic component is connected to the arachidonic acid residue via a nucleobase, a sugar or a phosphate group.
11. The conjugate of claim 1 , wherein r is an integer from 2-20.
12. The conjugate of claim 1 , wherein r is an integer from 2-8.
13. The conjugate of claim 1 , wherein n is an integer from 1-5.
14. The conjugate of claim 1 , wherein n is 1.
15. The conjugate of claim 6 , wherein the linker comprises a 1, 2, 3-triazole group, formed by a Click-reaction between an alkyne and an azide, or a group formed by a Click-reaction between a norbornene and a nitrile imine, a nitrile oxide or a tetrazine.
16. A reagent for manufacturing an RNA-ligand conjugate of the general formula (V):
F n -(L′) m -(RG1) r (V)
wherein
F is an arachidonic acid residue,
n is an integer from 1-10,
m is 0 or 1,
r is an integer from 1-25, L′ is a linker, and
RG1 is a Click-reactive group.
17. A reagent for manufacturing a nucleic acid conjugate having the general formula (VI):
BB-(L) m -F (VI)
wherein
F is an arachidonic acid residue,
L is a linker,
n is an integer from 1-10,
m is 0 or 1, and
BB is a building block for synthesizing a nucleic acid molecule or a building block suitable for solid phase synthesis.
18. A method of manufacturing a conjugate according to claim 1 , comprising
(i) coupling the reagent
BB-(L) m -F (VI)
with at least one modified RNA molecule (VII)
(N) r -(L″) m -RG2 (VII)
wherein
n is an integer from 1-10,
N is a nucleosidic component selected from nucleic acids, nucleosides and nucleotides,
is an integer from 1-25,
L″ is a linker,
m is 0 or 1, and
RG2 is a Click-reactive group capable of reacting with RG1, thereby forming the conjugate, or
(ii) coupling the reagent
F n -(L′) m -(RG1) r (V)
with at least one modified nucleic acid building block (VIII)
BB-(L″) m -RG2 (VIII)
wherein
BB is a building block for synthesizing a nucleic acid molecule,
L″ is a linker,
m is 0 or 1, and
RG2 is a Click-reactive group capable of reacting with RG1,
and incorporating the building block having coupled thereto the reagent into a nucleic acid molecule, thereby forming the conjugate.