Linkers and co-coupling agents for optimization of oligonucleotide synthesis and purification on solid supports
A method of modulation of synthesis capacity on and cleavage properties of synthetic oligomers from solid support is described. The method utilizes linker molecules attached to a solid surface and co-coupling agents that have similar reactivities to the coupling compounds with the surface functional groups. The preferred linker molecules provide an increased density of polymers and more resistance to cleavage from the support surface. The method is particularly useful for synthesis of oligonucleotides, oligonucleotides microarrays, peptides, and peptide microarrays. The stable linkers are also coupled to anchor molecules for synthesis of DNA oligonucleotides using on support purification, eliminating time-consuming chromatography and metal cation presence. Oligonucleotides thus obtained can be directly used for mass analysis, DNA amplification and ligation, hybridization, and many other applications.
1. A compound having the following structure:
S—R 1 —R 2 —R 3 —R 4
wherein S is a substrate, R 1 is a non-cleavable linker group, R 2 an oligonucleotide, R 3 is an anchor, wherein said anchor comprises the structure —C(X)—C(Y), wherein X comprises —OPO 2 O—, Y is a nucleophile and wherein said structure is part of a ring moiety, and R 4 is absent or is a polymer, where R 2 and R 4 are the same or different.
2. The compound of claim 1 , wherein said linker is selected from group consisting of akyl linkers, polyethyleneglycol, amide, and alkylenyl linkers.
3. A method for synthesizing oligonucleotides comprising:
a) providing
i) a substrate;
ii) a plurality of non-cleavable linkers;
iii) a plurality of anchor moieties, wherein said anchor moieties comprise the structure —C(X)—C(Y), wherein X comprises —OPO 2 O—, Y is a nucleophile and wherein said structure is part of a ring moiety; and
iv) nucleotide monomers;
b) derivatizing said substrate with said plurality of non-cleavable linkers;
c) attaching said anchor moieties to said non-cleavable linkers; and
d) synthesizing a oligonucleotide on said plurality of anchor moieties from said monomers.
4. A method for synthesizing oligonucleotides comprising:
a) providing
i) a substrate;
ii) a plurality of non-cleavable linkers;
iii) a plurality of anchor moieties, wherein said anchor moieties comprise the structure —C(X)—C(Y), wherein X comprises —OPO 2 O—, Y is a nucleophile and wherein said structure is part of a ring moiety; and
iv) nucleotide monomers;
b) derivatizing said substrate with said plurality of non-cleavable linkers;
c) synthesizing a oligonucleotide on said plurality of anchor moieties from said monomers; and
d) attaching said anchor moieties to said substrates; and
e) synthesizing a oligonucleotide on said plurality of anchor moieties from said monomers.
5. The compound of claim 1 , wherein said polymer is a polynucleotide.
6. The compound of claim 5 , wherein said polynucleotide comprises a label.
7. The compound of claim 1 , wherein said polymer is a polyamino acid.
8. A method for synthesizing oligonucleotides comprising:
a) providing
i) a substrate;
ii) a plurality of stable linkers;
iii) a plurality of anchor moieties; and
iv) nucleotide monomers;
b) derivatizing said substrate with said plurality of stable linkers;
c) attaching said anchor moieties to said stable linkers, wherein said anchor moieties are attached to said linkers via coupling a 5′ phosphoramidite present within said anchor moieties to said linkers through a 5′-O—P-linkage;
d) attaching said nucleotide monomers to said stable linkers attached to said anchor moeities through an anchor 3′-O—P—O-3′ nucleotide attachment thereby creating a plurality of anchor 3′-O—P—O-3′ nucleotide moeities; and
e) synthesizing oligonucleotides on said plurality of anchor-nucleotide moieties from said monomers,
wherein anchor 3′-O—P—O-3′ nucleotide phosphodiester attachments are cleaved by a ribonuclease.
9. The method of claim 8 , wherein said ribonuclease is selected from the group consisting of RNase A, T 1 , and U 2 .
10. The method of claim 8 , wherein cleaving with said ribonuclease produces, an oligonucleotide comprising a 3′-OH.
11. The method of claim 8 , wherein the 3′ and 5′ ends of the cleaved phosphodiester attachments are further modified using a 5′ or 3′ exonuclease.
12. The method of claim 11 , wherein said 5′ or 3′ exonuclease removes a terminal phosphate group.