A protected biotin containing deoxycytidine building block for solid phase synthesis of biotinylated oligonucleotides
Author(s) -
Uwe Pieles,
Brian S. Sproat,
Gábor M. Lamm
Publication year - 1990
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/18.15.4355
Subject(s) - biotinylation , biotin , oligonucleotide , streptavidin , moiety , combinatorial chemistry , biology , biochemistry , solid phase synthesis , agarose , dna , stereochemistry , chemistry , peptide
The synthesis of a modified 2'-deoxycytidine-3'-O-phosphoramidite carrying an N-t-butylbenzoyl protected biotin on a long polar spacer arm attached to the 4-N position is described. The presence of the bulky lipophilic t-butylbenzoyl protecting group enables the direct solid phase synthesis of biotinylated oligoribonucleotides and a variety of analogues in high yield without modification of the biotin moiety. Biotinylated antisense oligonucleotides incorporating this new derivative allow convenient isolation and purification of ribonucleic acid-protein complexes. The kinetics of biotin binding to streptavidin agarose is facilitated by the long polar spacer arm.
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