Repurpsing Antiviral Drugs for Orthogonal RNA-Catalyzed Labeling
Zitieren Sie bitte immer diese URN: urn:nbn:de:bvb:20-opus-205552
- In vitro selected ribozymes are promising tools for site-specific labeling of RNA. Previously known nucleic acid catalysts attached fluorescently labeled adenosine or guanosine derivatives through 2’,5’-branched phosphodiester bonds to the RNA of interest. Herein, we report new ribozymes that use orthogonal substrates, derived from the antiviral drug tenofovir, and attach bioorthogonal functional groups, as well as affinity handles and fluorescent reporter units through a hydrolytically more stable phosphonate ester linkage. The tenofovirIn vitro selected ribozymes are promising tools for site-specific labeling of RNA. Previously known nucleic acid catalysts attached fluorescently labeled adenosine or guanosine derivatives through 2’,5’-branched phosphodiester bonds to the RNA of interest. Herein, we report new ribozymes that use orthogonal substrates, derived from the antiviral drug tenofovir, and attach bioorthogonal functional groups, as well as affinity handles and fluorescent reporter units through a hydrolytically more stable phosphonate ester linkage. The tenofovir transferase ribozymes were identified by in vitro selection and are orthogonal to nucleotide transferase ribozymes. As genetically encodable functional RNAs, these ribozymes may be developed for potential cellular applications. The orthogonal ribozymes addressed desired target sites in large RNAs in vitro, as shown by fluorescent labeling of E. coli 16S and 23S RNAs in total cellular RNA.…
Autor(en): | Mohammad Ghaem Maghami, Surjendu Dey, Ann-Kathrin Lenz, Claudia HöbartnerORCiD |
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URN: | urn:nbn:de:bvb:20-opus-205552 |
Dokumentart: | Artikel / Aufsatz in einer Zeitschrift |
Institute der Universität: | Fakultät für Chemie und Pharmazie / Institut für Organische Chemie |
Sprache der Veröffentlichung: | Englisch |
Titel des übergeordneten Werkes / der Zeitschrift (Englisch): | Angewandte Chemie, International Edition |
Erscheinungsjahr: | 2020 |
Band / Jahrgang: | 59 |
Seitenangabe: | 9335–9339 |
Originalveröffentlichung / Quelle: | Angewandte Chemie, International Edition 2020, 59 , 9335-9339. https://doi.org/10.1002/anie.202001300 |
DOI: | https://doi.org/10.1002/anie.202001300 |
Allgemeine fachliche Zuordnung (DDC-Klassifikation): | 5 Naturwissenschaften und Mathematik / 54 Chemie / 547 Organische Chemie |
Freie Schlagwort(e): | Antiviral nucleoside analogues; in vitro selection; ribozymes; site-specific RNA labeling; tenofovir |
Datum der Freischaltung: | 09.06.2020 |
EU-Projektnummer / Contract (GA) number: | 682586 |
OpenAIRE: | OpenAIRE |
Lizenz (Deutsch): | CC BY-NC-ND: Creative-Commons-Lizenz: Namensnennung, Nicht kommerziell, Keine Bearbeitungen 4.0 International |