Abstract A process of producing synthetic oligonucleotides on a small or large scale using H-phosphonate nucleoside monomers is described. The process can be used to synthesize oligonucleotides of any length, including oligodeoxyribonucleotides and oligoribonucleotides. The process results in a coupling efficiency of greater than 97% and consumes only two to three equivalents of monomer to activator per coupling reaction. In addition, the process does not require a separate capping step and capping reagent because the activating reagent serves a self-capping function thereby preventing elongation of failed sequences. The H-phosphonate linkages of the fully synthesized oligonucleotide can be oxidized with a variety of reagents to obtain either phosphate diester or other types of modified oligonucleotides.
An improved process for synthesizing oligonucleotides by condensing a solid support-bound nucleotide with free activated nucleoside H-phosphonate monomer, wherein the improvement comprises producing the activated nucleoside H-phosphonate monomer by combining nucleoside H-phosphonate monomer and an activator in a ratio of less than one part monomer to five parts activator, and allowing the activated nucleoside H-phosphonate to react with the solid support-bound nucleotide for about 15 seconds or less.
Claim 2
Dependent Claim
68 words
An improved process for synthesizing oligonucleotides by condensing a solid support-bound nucleotide with free activated nucleoside H-phosphonate monomer, wherein the improvement comprises producing the activated nucleoside H-phosphonate monomer by combining nucleoside H-phosphonate monomer and an activator in a ratio of less than one part monomer to five parts activator, and allowing the activated nucleoside H-phosphonate to react with the solid support-bound nucleotide for about 15 seconds or less.
Claim 3
Dependent Claim
24 words
The improved process according to claim 1, wherein the ratio of H-phosphonate monomer to activator is one part monomer to about ten parts activator.