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Engineered Ribonucleoprotein Granules Inhibit Translation in Protocells.
Simon, Joseph R; Eghtesadi, Seyed Ali; Dzuricky, Michael; You, Lingchong; Chilkoti, Ashutosh.
Affiliation
  • Simon JR; NSF Research Triangle Materials Research Science and Engineering Center, Duke University, Durham, NC 27708, USA; Department of Biomedical Engineering, Duke University, Durham, NC 27708, USA.
  • Eghtesadi SA; NSF Research Triangle Materials Research Science and Engineering Center, Duke University, Durham, NC 27708, USA.
  • Dzuricky M; NSF Research Triangle Materials Research Science and Engineering Center, Duke University, Durham, NC 27708, USA; Department of Biomedical Engineering, Duke University, Durham, NC 27708, USA.
  • You L; Department of Biomedical Engineering, Duke University, Durham, NC 27708, USA; Center for Genomic and Computational Biology, Duke University, Durham, NC 27708, USA; Department of Molecular Genetics and Microbiology, Duke University School of Medicine, Durham, NC 27710, USA.
  • Chilkoti A; NSF Research Triangle Materials Research Science and Engineering Center, Duke University, Durham, NC 27708, USA; Department of Biomedical Engineering, Duke University, Durham, NC 27708, USA. Electronic address: ashutosh.chilkoti@duke.edu.
Mol Cell ; 75(1): 66-75.e5, 2019 07 11.
Article in En | MEDLINE | ID: mdl-31175012
ABSTRACT
Liquid granules rich in intrinsically disordered proteins and RNA play key roles in critical cellular functions such as RNA processing and translation. Many details of the mechanism via which this occurs remain to be elucidated. Motivated by the lacuna in the field and by the prospects of developing de novo artificial granules that provide extrinsic control of translation, we report a bottom-up approach to engineer ribonucleoprotein granules composed of a recombinant RNA-binding IDP that exhibits phase behavior in water. We developed a kinetic model to illustrate that these granules inhibit translation through reversible or irreversible sequestration of mRNA. Within monodisperse droplets capable of transcription and translation, we experimentally demonstrate temporal inhibition of translation by using designer IDPs that exhibit tunable phase behavior. This work lays the foundation for developing artificial granules that promise to further our mechanistic understanding of their naturally occurring counterparts.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ribonucleoproteins / RNA, Messenger / Cytoplasmic Granules / Peptidomimetics / Artificial Cells / Intrinsically Disordered Proteins Language: En Journal: Mol Cell Journal subject: BIOLOGIA MOLECULAR Year: 2019 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ribonucleoproteins / RNA, Messenger / Cytoplasmic Granules / Peptidomimetics / Artificial Cells / Intrinsically Disordered Proteins Language: En Journal: Mol Cell Journal subject: BIOLOGIA MOLECULAR Year: 2019 Type: Article Affiliation country: United States