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Projekt Druckansicht

Entschlüsselung des Mechanismus der Nukleotidselektion, -addition und des Proofreadings des SARS- Coronavirus Replikations-Transkriptionskomplexes auf Single Molecule Ebene

Antragsteller David Dulin, Ph.D.
Fachliche Zuordnung Virologie
Biophysik
Förderung Förderung von 2020 bis 2024
Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 447835095
 
Erstellungsjahr 2024

Zusammenfassung der Projektergebnisse

One of the key antiviral targets against coronaviruses (CoVs), such as SARS-CoV-1 and SARS-CoV-2, is their replication-transcription complex (RTC), a large complex made of several non-structural proteins (nsp) encoded in the coronavirus genome that synthesizes all the viral RNA in the infected cell. The RTC is made of core, constituted of nsp12-polymerase with its associated co-factors nsp7 and nsp8 in a 1:1:2 stoichiometry, to which associates e.g. nsp9, the nsp13-helicase, the exonuclease (ExoN)-methyltransferase nsp14. When this proposal was submitted, in February 2020, little was known about the structure and the functional role of each factor composing the CoV RTC. The goal of this proposal was to determine the nucleotide addition cycle of the core RTC, the mechanism of action of different nucleotide analogs on the RTC elongation dynamics, and to decipher how nsp14-ExoN assists the RTC in proofreading, which protects CoV replication in infected cell against many existing approved nucleotide analogs. Structural advances in the knowledge related to the complex assembly after the proposal submission directed my research towards the RTC assembly and revealing the role of nsp13-helicase during viral RNA synthesis.

Projektbezogene Publikationen (Auswahl)

 
 

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