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Chemical Methods for Peptide-Oligonucleotide Conjugate Synthesis
Abstract
Methods of peptide-oligonucleotide conjugate synthesis are presented that may be useful in the study of cell targeting and delivery of oligonucleotides and their analogs. The first method involves total stepwise solid-phase synthesis on a single support. The second involves preparation of oligonucleotides containing 2′-aldehydes and subsequent chemoselective ligation with functionalized peptides to form hydrazine, oxime, or thiazolidine linkages.
Affiliation(s): (2) Laboratory of Molecular Biology, MRC, Cambridge, UK
Series: Methods in Molecular Biology  |  Volume: 288  |  Pub. Date: Sep-01-2004  |  Page Range: 205-224  |  DOI: 10.1385/1-59259-823-4:205
Subject:  Biochemistry
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