RNA monomers containing O-acetal levulinyl ester groups and their use in RNA microarrays
The present invention is directed to RNA monomers comprising O-acetal levulinyl protecting groups at the 2′ and/or the 5′-hydroxy functionalities of the ribose moiety. Said monomers may be incorporated into oligoribonucleotides or RNA polynucleotides. Furthermore, the invention is directed to methods for the synthesis of said RNA monomers, oligoribonucleotides and RNA polynucleotides, as well as methods for their deprotection and methods for the use of said compounds and compositions comprising said compounds. In particular, such compounds and compositions comprising them are used in methods for light-directed synthesis of RNA microarrays.
1. A compound of formula (I):
wherein
B is a member selected from the group consisting of 6-amino-9H-purin-9-yl, 2-amino-1H-purin-6(9H)-on-9-yl, 4-aminopyrimidin-2(1H)-on-1-yl, pyrimidine-2,4(1H,3H)-dion-1-yl, N4-levulinylcytosine, N2-levulinylguanine, N2-(dimethylformamidine)guanine, N2-phenoxyacetylguanine, N6-(tert-butylphenoxyacetypadenine, N6-(9-fluorenylmethoxycarbonyl)adenine, N2-(9-fluorenylmethoxycarbonyl)guanine, N4-benzoylcytosine, N6-benzoyladenine, N4-isobutyrylcytosine, N4-acetylcytosine, and N2-isobutyrylguanine;
P 1 is hydrogen or —CH 2 OC(O)CH 2 CH 2 C(O)CH 3 ;
P 2 is hydrogen or
or salts thereof, wherein R is methyl, 2-cyanoethyl, 2-chlorophenyl, or 4-chlorophenyl;
or
P 3 is hydrogen or an O-protecting group, which is a member selected from the group consisting of:
a. a base labile group selected from —CH 2 OC(O)CH 2 CH 2 C(O)CH 3 and —C(O)CH 2 CH 2 C(O)CH 3 ;
b. an acid labile group selected from 1-(2-fluorophenyl)-4-methoxypiperidin-4-yl, 1-(4-chlorophenyl)-4-ethoxypiperidin-4-yl, 4-(N-dichloroacetyl-N-methylamino)benzyloxymethyl, dimethoxytrityl and monomethoxytrityl;
c. a reduction labile group selected from 2-tert-butyldithiomethyl and allyl;
d. a fluoride labile group selected from tert-butyldimethylsilane, 2′-O-triisopropylsilyloxymethyl, cyanoethylmethyl, and 2-(4-tolylsulfonyl)ethoxymethyl; and
e. a photolabile group selected from 2-(2-nitrophenyl)propoxycarbonyl, α-methylnitorpiperonyloxycarbonyl, and 5′-O-dimethoxybenzoincarbonate; and
wherein at least one of P 1 and P 3 is —CH 2 OC(O)CH 2 CH 2 C(O)CH 3 as the O-protecting group.
2. The compound of claim 1 of formula (II):
3. The compound of claim 1 of formula (IV):
4. The compound of claim 1 of formula (V):
5. The compound of claim 1 of formula (VI):
6. The compound of claim 1 , wherein B is a member selected from the group consisting of 6-amino-9H-purin-9-yl, 2-amino-1H-purin-6(9H)-on-9-yl, 4-aminopyrimidin-2(1H)-on-1-yl, and pyrimidine-2,4(1H,3H)-dion-1-yl.
7. The compound of claim 1 , wherein B is a member selected from the group consisting of N4-levulinylcytosine, N2-levulinylguanine, N2-(dimethylformamidine)guanine, N2-phenoxyacetylguanine, N6-(tert-butylphenoxyacetypadenine, N6-(9-fluorenylmethoxycarbonyl)adenine, N2-(9-fluorenylmethoxycarbonyl)guanine, N4-benzoylcytosine, N6-benzoyladenine, N4-isobutyrylcytosine, N4-acetylcytosine, and N2-isobutyrylguanine.
8. A compound comprising an RNA monomer of formula (I):
wherein
B is a member selected from the group consisting of 6-amino-9H-purin-9-yl, 2-amino-1H-purin-6(9H)-on-9-yl, 4-aminopyrimidin-2(1H)-on-1-yl, pyrimidine-2,4(1H,3H)-dion-1-yl, N4-levulinylcytosine, N2-levulinylguanine, N2-(dimethylformamidine)guanine, N2-phenoxyacetylguanine, N6-(tert-butylphenoxyacetypadenine, N6-(9-fluorenylmethoxycarbonyl)adenine, N2-(9-fluorenylmethoxycarbonyl)guanine, N4-benzoylcytosine, N6-benzoyladenine, N4-isobutyrylcytosine, N4-acetylcytosine, and N2-isobutyrylguanine;
P 2 is hydrogen or
or salts thereof, wherein R is methyl, 2-cyanoethyl, 2-chlorophenyl, or 4-chlorophenyl;
or
P 1 is a 2′-O-acetal levulinyl ester protecting group;
and P 3 is a 5′-2-(2-nitrophenyl)propoxycarbonyl protecting group.
9. The compound of claim 8 wherein the RNA monomer is immobilized on a solid substrate.
10. An RNA oligonucleotide comprising at least one RNA monomer of formula (I):
wherein
B is a member selected from the group consisting of 6-amino-9H-purin-9-yl, 2-amino-1H-purin-6(9H)-on-9-yl, 4-aminopyrimidin-2(1H)-on-1-yl, pyrimidine-2,4(1H,3H)-dion-1-yl, N4-levulinylcytosine, N2-levulinylguanine, N2-(dimethylformamidine)guanine, N2-phenoxyacetylguanine, N6-(tert-butylphenoxyacetypadenine, N6-(9-fluorenylmethoxycarbonyl)adenine, N2-(9-fluorenylmethoxycarbonyl)guanine, N4-benzoylcytosine, N6-benzoyladenine, N4-isobutyrylcytosine, N4-acetylcytosine, and N2-isobutyrylguanine;
P 2 is hydrogen or
or salts thereof, wherein R is methyl, 2-cyanoethyl, 2-chlorophenyl, or 4-chlorophenyl;
or
P 1 is a 2′-O-acetal levulinyl ester protecting group; and
P 3 is a 5′-2-(2-nitrophenyl)propoxycarbonyl protecting group.
11. The RNA oligonucleotide of claim 10 wherein the RNA oligonucleotide is immobilized on a solid substrate.
12. An array comprising at least two RNA oligonucleotides of different sequence immobilized on a solid substrate, wherein each RNA oligonucleotide comprises at least one RNA monomer of formula (I) according to claim 10 .
13. The array of claim 12 , wherein the monomer has a 2′-O-acetal levulinyl ester protecting group and a 5′-2-(2-nitrophenyl)propoxycarbonyl protecting group.