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De novo design of pH-responsive self-assembling helical protein filaments.
Shen, Hao; Lynch, Eric M; Akkineni, Susrut; Watson, Joseph L; Decarreau, Justin; Bethel, Neville P; Benna, Issa; Sheffler, William; Farrell, Daniel; DiMaio, Frank; Derivery, Emmanuel; De Yoreo, James J; Kollman, Justin; Baker, David.
Afiliación
  • Shen H; Department of Biochemistry, University of Washington, Seattle, WA, USA. shenh2@uw.edu.
  • Lynch EM; Institute for Protein Design, University of Washington, Seattle, WA, USA. shenh2@uw.edu.
  • Akkineni S; Department of Biochemistry, University of Washington, Seattle, WA, USA.
  • Watson JL; Department of Materials Science and Engineering, University of Washington, Seattle, WA, USA.
  • Decarreau J; Physical Sciences Division, Pacific Northwest National Laboratory, Richland, WA, USA.
  • Bethel NP; Department of Biochemistry, University of Washington, Seattle, WA, USA.
  • Benna I; Institute for Protein Design, University of Washington, Seattle, WA, USA.
  • Sheffler W; MRC Laboratory of Molecular Biology, Cambridge, UK.
  • Farrell D; Department of Biochemistry, University of Washington, Seattle, WA, USA.
  • DiMaio F; Institute for Protein Design, University of Washington, Seattle, WA, USA.
  • Derivery E; Department of Biochemistry, University of Washington, Seattle, WA, USA.
  • De Yoreo JJ; Institute for Protein Design, University of Washington, Seattle, WA, USA.
  • Kollman J; Institute for Protein Design, University of Washington, Seattle, WA, USA.
  • Baker D; Department of Bioengineering, University of Washington, Seattle, WA, USA.
Nat Nanotechnol ; 2024 Apr 03.
Article en En | MEDLINE | ID: mdl-38570702
ABSTRACT
Biological evolution has led to precise and dynamic nanostructures that reconfigure in response to pH and other environmental conditions. However, designing micrometre-scale protein nanostructures that are environmentally responsive remains a challenge. Here we describe the de novo design of pH-responsive protein filaments built from subunits containing six or nine buried histidine residues that assemble into micrometre-scale, well-ordered fibres at neutral pH. The cryogenic electron microscopy structure of an optimized design is nearly identical to the computational design model for both the subunit internal geometry and the subunit packing into the fibre. Electron, fluorescent and atomic force microscopy characterization reveal a sharp and reversible transition from assembled to disassembled fibres over 0.3 pH units, and rapid fibre disassembly in less than 1 s following a drop in pH. The midpoint of the transition can be tuned by modulating buried histidine-containing hydrogen bond networks. Computational protein design thus provides a route to creating unbound nanomaterials that rapidly respond to small pH changes.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Nat Nanotechnol Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Nat Nanotechnol Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos