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De novo design of obligate ABC-type heterotrimeric proteins.
Bermeo, Sherry; Favor, Andrew; Chang, Ya-Ting; Norris, Andrew; Boyken, Scott E; Hsia, Yang; Haddox, Hugh K; Xu, Chunfu; Brunette, T J; Wysocki, Vicki H; Bhabha, Gira; Ekiert, Damian C; Baker, David.
Afiliação
  • Bermeo S; Department of Biochemistry, University of Washington, Seattle, WA, USA.
  • Favor A; Institute for Protein Design, University of Washington, Seattle, WA, USA.
  • Chang YT; Biological Physics, Structure and Design Graduate Program, University of Washington, Seattle, WA, USA.
  • Norris A; Department of Biochemistry, University of Washington, Seattle, WA, USA.
  • Boyken SE; Institute for Protein Design, University of Washington, Seattle, WA, USA.
  • Hsia Y; Molecular Engineering and Sciences Institute, University of Washington, Seattle, WA, USA.
  • Haddox HK; Department of Cell Biology, New York University School of Medicine, New York, NY, USA.
  • Xu C; Department of Chemistry and Biochemistry, The Ohio State University, Columbus, OH, USA.
  • Brunette TJ; Resource for Native Mass Spectrometry Guided Structural Biology, The Ohio State University, Columbus, OH, USA.
  • Wysocki VH; Department of Biochemistry, University of Washington, Seattle, WA, USA.
  • Bhabha G; Institute for Protein Design, University of Washington, Seattle, WA, USA.
  • Ekiert DC; Department of Biochemistry, University of Washington, Seattle, WA, USA.
  • Baker D; Institute for Protein Design, University of Washington, Seattle, WA, USA.
Nat Struct Mol Biol ; 29(12): 1266-1276, 2022 12.
Article em En | MEDLINE | ID: mdl-36522429
ABSTRACT
The de novo design of three protein chains that associate to form a heterotrimer (but not any of the possible two-chain heterodimers) and that can drive the assembly of higher-order branching structures is an important challenge for protein design. We designed helical heterotrimers with specificity conferred by buried hydrogen bond networks and large aromatic residues to enhance shape complementary packing. We obtained ten designs for which all three chains cooperatively assembled into heterotrimers with few or no other species present. Crystal structures of a helical bundle heterotrimer and extended versions, with helical repeat proteins fused to individual subunits, showed all three chains assembling in the designed orientation. We used these heterotrimers as building blocks to construct larger cyclic oligomers, which were structurally validated by electron microscopy. Our three-way junction designs provide new routes to complex protein nanostructures and enable the scaffolding of three distinct ligands for modulation of cell signaling.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas Idioma: En Revista: Nat Struct Mol Biol Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas Idioma: En Revista: Nat Struct Mol Biol Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos