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 Resjournal_title
Nucleic acids researchauthors
Pon RT,Yu Sdoi
10.1093/nar/gkh222keywords:
subject
Has Abstractpub_date
2004-01-29 00:00:00pages
623-31issue
2eissn
0305-1048issn
1362-4962pii
32/2/623journal_volume
32pub_type
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