Evidence map›Paper›PMID 39747896›Full record

ArticleNature communications2025

Programming scheduled self-assembly of circadian materials.

Gregor Leech, Lauren Melcher, Michelle Chiu, Maya Nugent, Shirlaine Juliano, Lily Burton, Janet Kang, Soo Ji Kim, Sourav Roy, Leila Farhadi and 4 more

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Gregor LeechDepartment of Physics and Biophysics, University of San Diego, San Diego, CA, USA.
Lauren Melcher *School of Mathematical Sciences, Rochester Institute of Technology, Rochester, NY, USA.
Michelle Chiu *Graduate Program in Biophysical Sciences, University of Chicago, Chicago, IL, USA.
Maya NugentDepartment of Physics and Biophysics, University of San Diego, San Diego, CA, USA.
Shirlaine JulianoDepartment of Physics and Biophysics, University of San Diego, San Diego, CA, USA.
Lily BurtonDepartment of Biochemistry and Molecular Biophysics, University of Chicago, Chicago, IL, USA.
Janet KangDepartment of Molecular Genetics and Cell Biology and Department of Physics, University of Chicago, Chicago, IL, USA.
Soo Ji KimDepartment of Biochemistry and Molecular Biophysics, University of Chicago, Chicago, IL, USA.
Sourav RoyDepartment of Physics, Syracuse University, Syracuse, NY, USA.
Leila FarhadiDepartment of Physics, Syracuse University, Syracuse, NY, USA.
Jennifer L RossDepartment of Physics, Syracuse University, Syracuse, NY, USA.
Moumita DasSchool of Mathematical Sciences, Rochester Institute of Technology, Rochester, NY, USA.ORCID 0000-0002-0397-8886
Michael J RustDepartment of Molecular Genetics and Cell Biology and Department of Physics, University of Chicago, Chicago, IL, USA.ORCID 0000-0002-7207-4020
Rae M Robertson-AndersonDepartment of Physics and Biophysics, University of San Diego, San Diego, CA, USA. randerson@sandiego.edu.ORCID 0000-0003-4475-4667

Funding

Coupling between Circadian Rhythms and Metaboilsm in CyanobacteriaR01GM107369 · NIGMS · UNIVERSITY OF CHICAGO · PI RUST, MICHAEL · 2013 to 2017
$1.5M
National Science Foundation (NSF) DMR-2118403National Science Foundation (NSF) DMR-2118424National Science Foundation (NSF) DMR-2118449National Science Foundation (NSF) DMR-2119663NIGMS NIH HHS R01 GM107369Research Corporation for Scientific Advancement (RCSA) CS-PBP-2023-019
6 · The paper itself

Abstract

Active biological molecules present a powerful, yet largely untapped, opportunity to impart autonomous regulation of 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 for oscillatory 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.

Indexed as

ColloidsCircadian ClocksCircadian Rhythm Signaling Peptides and ProteinsKineticsPhosphorylationCircadian Rhythm Signaling Peptides and ProteinsColloids

Identifiers

PMID39747896
PMCPMC11696221

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.