Linker phosphoramidite reagents for the attachment of the first nucleoside to underivatized solid-phase supports.

Abstract:

:New linker phosphoramidite reagents containing a cleavable 3'-ester linkage are used for attaching the first nucleoside to the surface of a solid- phase support. Inexpensive, underivatized amino supports, such as long chain alkylamine controlled-pore glass, can serve as universal supports. No modifications to phosphoramidite coupling conditions are required and, after synthesis, treatment with NH(4)OH releases the products with 3'-OH ends. No 3'-dephosphorylation is required. Phosphoramidite reagents containing a succinate and sulfonyl diethanol linkage between the nucleoside and phosphoramidite group are particularly advantageous and can be used to create both 3'-OH and 5'-phosphate ends on oligonucleotides. Reproducibility and quality of oligonucleotide synthesis is demonstrated for either column and 96-well plate formats on low-, medium- or high-loading CPG supports.

journal_name

Nucleic Acids Res

journal_title

Nucleic acids research

authors

Pon RT,Yu S

doi

10.1093/nar/gkh222

keywords:

subject

Has Abstract

pub_date

2004-01-29 00:00:00

pages

623-31

issue

2

eissn

0305-1048

issn

1362-4962

pii

32/2/623

journal_volume

32

pub_type

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