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Improved protein splicing through viral passaging.
Hume, Adam J; Deeney, Dylan J; Smetana, John S; Turcinovic, Jacquelyn; Connor, John H; Belfort, Marlene; Mühlberger, Elke; Lennon, Christopher W.
Afiliación
  • Hume AJ; Department of Microbiology, Boston University School of Medicine, Boston, Massachusetts, USA.
  • Deeney DJ; National Emerging Infectious Diseases Laboratories, Boston University, Boston, Massachusetts, USA.
  • Smetana JS; Center for Emerging Infectious Diseases Policy & Research, Boston University, Boston, Massachusetts, USA.
  • Turcinovic J; Department of Microbiology, Boston University School of Medicine, Boston, Massachusetts, USA.
  • Connor JH; National Emerging Infectious Diseases Laboratories, Boston University, Boston, Massachusetts, USA.
  • Belfort M; Department of Biological Sciences, Murray State University, Murray, Kentucky, USA.
  • Mühlberger E; Department of Microbiology, Boston University School of Medicine, Boston, Massachusetts, USA.
  • Lennon CW; National Emerging Infectious Diseases Laboratories, Boston University, Boston, Massachusetts, USA.
mBio ; 15(6): e0098424, 2024 Jun 12.
Article en En | MEDLINE | ID: mdl-38780266
ABSTRACT
Intervening proteins (inteins) are translated as subdomains within host proteins and removed through an intein-driven splicing reaction where the flanking sequences (exteins) are joined with a peptide bond. Previously, we developed a self-removing translation reporter for labeling Ebola virus (EBOV). In this reporter, an intein (RadA) containing the fluorescent protein ZsGreen (ZsG) is inserted within the EBOV protein VP30. Upon VP30-RadA-ZsG expression from the viral genome, RadA-ZsG is removed from VP30 through the protein splicing activity of RadA, generating functional, non-tagged VP30 and functional ZsGreen. While incorporation of our VP30-RadA-ZsG fusion reporter into recombinant EBOV (rEBOV-RadA-ZsG) resulted in an infectious virus that expresses ZsG upon infection of cells, this virus displayed a replication defect compared to wild-type EBOV, which might be the result of insufficient RadA splicing. Here, we demonstrate that the serial passaging of rEBOV-RadA-ZsG in human cells led to an increase in replication efficiency compared to unpassaged rEBOV-RadA-ZsG. Sequencing of passaged viruses revealed intein-specific mutations. These mutations improve intein activity in both prokaryotic and eukaryotic systems, as well as in multiple extein contexts. Taken together, our findings offer a novel means to select for inteins with enhanced catalytic properties that appear independent of extein context and expression system.IMPORTANCEIntervening proteins (inteins) are self-removing protein elements that have been utilized to develop a variety of innovative protein engineering technologies. Here, we report the isolation of inteins with improved catalytic activity through viral passaging. Specifically, we inserted a highly active intein within an essential protein of Ebola virus and serially passaged this recombinant virus, which led to intein-specific hyper-activity mutations. The identified mutations showed improved intein activity within both bacterial and eukaryotic expression systems and in multiple extein contexts. These results present a new strategy for developing inteins with improved splicing activity.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Empalme de Proteína / Inteínas / Ebolavirus Límite: Humans Idioma: En Revista: MBio Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Empalme de Proteína / Inteínas / Ebolavirus Límite: Humans Idioma: En Revista: MBio Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos