Nucleobase-involved native chemical ligation: a novel reaction between an oxanine nucleobase and N-terminal cysteine for oligonucleotide-peptide conjugation

In bioconjugation chemistry, achieving a target-specific reaction for a non-modified amino acid is challenging. Here, we report a novel nucleobase-involved native chemical ligation (NbCL) that allows a site-specific oligonucleotide-peptide conjugation via a new S-N acyl transfer reaction between an...

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Veröffentlicht in:Chemical communications (Cambridge, England) England), 2020-05, Vol.56 (41), p.5508-5511
Hauptverfasser: Jang, Eui Kyoung, Koike, Yohei, Ide, Yuko, Tajima, Kunihiko, Kanaori, Kenji, Pack, Seung Pil
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Sprache:eng
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Zusammenfassung:In bioconjugation chemistry, achieving a target-specific reaction for a non-modified amino acid is challenging. Here, we report a novel nucleobase-involved native chemical ligation (NbCL) that allows a site-specific oligonucleotide-peptide conjugation via a new S-N acyl transfer reaction between an oxanine nucleobase and N-terminal cysteine.
ISSN:1359-7345
1364-548X
DOI:10.1039/c9cc08808c