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Timed material self-assembly controlled by circadian clock proteins.
Leech, Gregor; Melcher, Lauren; Chiu, Michelle; Nugent, Maya; Burton, Lily; Kang, Janet; Kim, Soo Ji; Roy, Sourav; Farhadi, Leila; Ross, Jennifer L; Das, Moumita; Rust, Michael J; Robertson-Anderson, Rae M.
Afiliación
  • Leech G; Department of Physics and Biophysics, University of San Diego, San Diego, California 92110, United States.
  • Melcher L; School of Mathematical Sciences, Rochester Institute of Technology, Rochester, New York 14623, United States.
  • Chiu M; Graduate Program in Biophysical Sciences, University of Chicago, Chicago, Illinois 60637, United States.
  • Nugent M; Department of Physics and Biophysics, University of San Diego, San Diego, California 92110, United States.
  • Burton L; Department of Biochemistry and Molecular Biophysics, University of Chicago, Chicago, Illinois 60637, United States.
  • Kang J; Department of Molecular Genetics and Cell Biology and Department of Physics, University of Chicago, Chicago, Illinois 60637, United States.
  • Kim SJ; Department of Biochemistry and Molecular Biophysics, University of Chicago, Chicago, Illinois 60637, United States.
  • Roy S; Department of Physics, Syracuse University, Syracuse, New York 13244, United States.
  • Farhadi L; Department of Physics, Syracuse University, Syracuse, New York 13244, United States.
  • Ross JL; Department of Physics, Syracuse University, Syracuse, New York 13244, United States.
  • Das M; School of Mathematical Sciences, Rochester Institute of Technology, Rochester, New York 14623, United States.
  • Rust MJ; School of Physics and Astronomy, Rochester Institute of Technology, Rochester, New York 14623, United States.
  • Robertson-Anderson RM; Department of Molecular Genetics and Cell Biology and Department of Physics, University of Chicago, Chicago, Illinois 60637, United States.
ArXiv ; 2024 Mar 21.
Article en En | MEDLINE | ID: mdl-36911279
ABSTRACT
Active biological molecules present a powerful, yet largely untapped, opportunity to impart autonomous regulation to materials. Because these systems can function robustly to regulate when and where chemical reactions occur, they have the ability to bring complex, life-like behavior to synthetic materials. Here, we achieve this design feat by using functionalized circadian clock proteins, KaiB and KaiC, to engineer time-dependent crosslinking of colloids. The resulting material self-assembles with programmable kinetics, producing macroscopic changes in material properties, via molecular assembly of KaiB-KaiC complexes. We show that colloid crosslinking depends strictly on the phosphorylation state of KaiC, with kinetics that are synced with KaiB-KaiC complexing. Our microscopic image analyses and computational models indicate that the stability of colloidal super-structures depends sensitively on the number of Kai complexes per colloid connection. Consistent with our model predictions, a high concentration stabilizes the material against dissolution after a robust self-assembly phase, while a low concentration allows circadian oscillation of material structure. This work introduces the concept of harnessing biological timers to control synthetic materials; and, more generally, opens the door to using protein-based reaction networks to endow synthetic systems with life-like functional properties.

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: ArXiv Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: ArXiv Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos