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Mitochondria and Peroxisome Remodeling across Cytomegalovirus Infection Time Viewed through the Lens of Inter-ViSTA.
Federspiel, Joel D; Cook, Katelyn C; Kennedy, Michelle A; Venkatesh, Samvida S; Otter, Clayton J; Hofstadter, William A; Jean Beltran, Pierre M; Cristea, Ileana M.
Afiliação
  • Federspiel JD; Department of Molecular Biology, Princeton University, Washington Road, Princeton, NJ 08544, USA.
  • Cook KC; Department of Molecular Biology, Princeton University, Washington Road, Princeton, NJ 08544, USA.
  • Kennedy MA; Department of Molecular Biology, Princeton University, Washington Road, Princeton, NJ 08544, USA.
  • Venkatesh SS; Department of Molecular Biology, Princeton University, Washington Road, Princeton, NJ 08544, USA.
  • Otter CJ; Department of Molecular Biology, Princeton University, Washington Road, Princeton, NJ 08544, USA.
  • Hofstadter WA; Department of Molecular Biology, Princeton University, Washington Road, Princeton, NJ 08544, USA.
  • Jean Beltran PM; Department of Molecular Biology, Princeton University, Washington Road, Princeton, NJ 08544, USA.
  • Cristea IM; Department of Molecular Biology, Princeton University, Washington Road, Princeton, NJ 08544, USA. Electronic address: icristea@princeton.edu.
Cell Rep ; 32(4): 107943, 2020 07 28.
Article em En | MEDLINE | ID: mdl-32726614
ABSTRACT
Nearly all biological processes rely on the finely tuned coordination of protein interactions across cellular space and time. Accordingly, generating protein interactomes has become routine in biological studies, yet interpreting these datasets remains computationally challenging. Here, we introduce Inter-ViSTA (Interaction Visualization in Space and Time Analysis), a web-based platform that quickly builds animated protein interaction networks and automatically synthesizes information on protein abundances, functions, complexes, and subcellular localizations. Using Inter-ViSTA with proteomics and molecular virology, we define virus-host interactions for the human cytomegalovirus (HCMV) anti-apoptotic protein, pUL37x1. We find that spatiotemporal controlled interactions underlie pUL37x1 functions, facilitating the pro-viral remodeling of mitochondria and peroxisomes during infection. Reciprocal isolations, microscopy, and genetic manipulations further characterize these associations, revealing the interplay between pUL37x1 and the MIB complex, which is critical for mitochondrial integrity. At the peroxisome, we show that pUL37x1 activates PEX11ß to regulate fission, a key aspect of virus assembly and spread.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Biologia Computacional / Mapas de Interação de Proteínas / Mitocôndrias Limite: Humans Idioma: En Revista: Cell Rep Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Biologia Computacional / Mapas de Interação de Proteínas / Mitocôndrias Limite: Humans Idioma: En Revista: Cell Rep Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Estados Unidos