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Timed material self-assembly controlled by circadian clock proteins

Biological systems 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. H...

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Autores principales: Leech, Gregor, Melcher, Lauren, Chiu, Michelle, Nugent, Maya, Burton, Lily, Kang, Janet, Kim, Soo Ji, Roy, Sourav, Farhadi, Laila, Ross, Jennifer L., Das, Moumita, Rust, Michael J., Robertson-Anderson, Rae M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cornell University 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10002811/
https://www.ncbi.nlm.nih.gov/pubmed/36911279
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author Leech, Gregor
Melcher, Lauren
Chiu, Michelle
Nugent, Maya
Burton, Lily
Kang, Janet
Kim, Soo Ji
Roy, Sourav
Farhadi, Laila
Ross, Jennifer L.
Das, Moumita
Rust, Michael J.
Robertson-Anderson, Rae M.
author_facet Leech, Gregor
Melcher, Lauren
Chiu, Michelle
Nugent, Maya
Burton, Lily
Kang, Janet
Kim, Soo Ji
Roy, Sourav
Farhadi, Laila
Ross, Jennifer L.
Das, Moumita
Rust, Michael J.
Robertson-Anderson, Rae M.
author_sort Leech, Gregor
collection PubMed
description Biological systems 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 self-assembly of colloidal super-structures requires multiple Kai complexes per colloid connection, which then stabilizes the material against dissolution. 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.
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spelling pubmed-100028112023-03-11 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, Laila Ross, Jennifer L. Das, Moumita Rust, Michael J. Robertson-Anderson, Rae M. ArXiv Article Biological systems 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 self-assembly of colloidal super-structures requires multiple Kai complexes per colloid connection, which then stabilizes the material against dissolution. 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. Cornell University 2023-03-01 /pmc/articles/PMC10002811/ /pubmed/36911279 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use.
spellingShingle Article
Leech, Gregor
Melcher, Lauren
Chiu, Michelle
Nugent, Maya
Burton, Lily
Kang, Janet
Kim, Soo Ji
Roy, Sourav
Farhadi, Laila
Ross, Jennifer L.
Das, Moumita
Rust, Michael J.
Robertson-Anderson, Rae M.
Timed material self-assembly controlled by circadian clock proteins
title Timed material self-assembly controlled by circadian clock proteins
title_full Timed material self-assembly controlled by circadian clock proteins
title_fullStr Timed material self-assembly controlled by circadian clock proteins
title_full_unstemmed Timed material self-assembly controlled by circadian clock proteins
title_short Timed material self-assembly controlled by circadian clock proteins
title_sort timed material self-assembly controlled by circadian clock proteins
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10002811/
https://www.ncbi.nlm.nih.gov/pubmed/36911279
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