Synthesis of Peptide‐Oligonucleotide Conjugates Using a Heterobifunctional Crosslinker

Peptide‐oligonucleotide conjugates (POCs) are molecular chimeras composed of a nucleic acid moiety covalently attached to a polypeptide moiety. POCs have been used in numerous applications from therapeutics to nanotechnology, and most recently as combinatorial agents in the assembly of bivalent prot...

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Veröffentlicht in:Current Protocols in Nucleic Acid Chemistry 2010-09, Vol.42 (1), p.4.41.1-4.41.20
Hauptverfasser: Williams, Berea A.R., Chaput, John C.
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Sprache:eng
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Zusammenfassung:Peptide‐oligonucleotide conjugates (POCs) are molecular chimeras composed of a nucleic acid moiety covalently attached to a polypeptide moiety. POCs have been used in numerous applications from therapeutics to nanotechnology, and most recently as combinatorial agents in the assembly of bivalent protein affinity reagents. This unit describes the synthesis and purification of POC molecules using the heterobifunctional crosslinking reagent succinimidyl‐4‐(N‐maleimidomethyl)cyclohexane‐1‐carboxylate (SMCC), which enables amine‐modified oligonucleotides to become covalently linked to cysteine‐modified polypeptides. This solution‐based protocol consists of a two‐step synthesis followed by a single purification step. Curr. Protoc. Nucleic Acid Chem. 42:4.41.1‐4.41.20. © 2010 by John Wiley & Sons, Inc.
ISSN:1934-9270
1934-9289
DOI:10.1002/0471142700.nc0441s42