Linkers and co-coupling agents for optimization of oligonucleotide synthesis and purification on solid supports

摘要

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.

主权项

1. A method for synthesizing oligonucleotides at predetermined sites on a substrate 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 —OPO2O—, Y is a nucleophile and wherein said structure is part of a ring moiety;iv) nucleotide monomers; andv) co-coupling agents; b) derivatizing said substrate with said plurality of non-cleavable linkers; c) attaching said anchor moieties to said non-cleavable linkers to form a plurality of substrate-linker group-anchor group moieties; and d) synthesizing, utilizing said monomers and co-coupling agents, an oligonucleotide on each of said plurality of substrate-linker group-anchor group moieties.