Rapid Synthesis of Nucleoside Triphosphates and Analogues.

cyclotriphosphate non-hydrolyzable nucleotide analogues nucleoside 5′-triphosphate phosphoramidite phosphorylation

Journal

Current protocols in nucleic acid chemistry
ISSN: 1934-9289
Titre abrégé: Curr Protoc Nucleic Acid Chem
Pays: United States
ID NLM: 101287865

Informations de publication

Date de publication:
06 2020
Historique:
entrez: 12 5 2020
pubmed: 12 5 2020
medline: 4 5 2021
Statut: ppublish

Résumé

Nucleoside triphosphates (NTPs) are essential biomolecules involved in almost all biological processes, and their study is therefore critical to understanding cellular biology. Here, we describe a chemical synthesis suitable for obtaining both natural and highly modified NTPs, which can, for example, be used as surrogates to probe biological processes. The approach includes the preparation of a reagent that enables the facile introduction and modification of three phosphate units: cyclic pyrophosphoryl P-amidite (c-PyPA), derived from pyrophosphate (P

Identifiants

pubmed: 32391982
doi: 10.1002/cpnc.108
doi:

Substances chimiques

Nucleotides 0
Phosphates 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e108

Informations de copyright

© 2020 The Authors.

Références

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Auteurs

Alexander Ripp (A)

Institute of Organic Chemistry, University of Freiburg, Freiburg, Germany.
Cluster of Excellence livMatS @ FIT-Freiburg Center for Interactive Materials and Bioinspired Technologies, University of Freiburg, Freiburg, Germany.

Jyoti Singh (J)

Institute of Organic Chemistry, University of Freiburg, Freiburg, Germany.

Henning J Jessen (HJ)

Institute of Organic Chemistry, University of Freiburg, Freiburg, Germany.
Freiburg Research Institute for Advanced Studies, University of Freiburg, Freiburg, Germany.
Cluster of Excellence livMatS @ FIT-Freiburg Center for Interactive Materials and Bioinspired Technologies, University of Freiburg, Freiburg, Germany.

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