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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.
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http://dx.doi.org/10.1038/s41467-024-55645-5 | DOI Listing |
J Org Chem
September 2025
Jiangsu Key Laboratory of Green Synthetic Chemistry for Functional Materials, School of Chemistry and Materials Science, Jiangsu Normal University, Xuzhou, Jiangsu 221116, PR China.
A convenient protocol for the synthesis of selenated benzoxepine derivatives via iron(III)-catalyzed 7-endo-trig cyclization has been first established via reaction of 1,7-diene containing nonactivated allyl and dialkyl diselenides under room temperature and air conditions. Research has shown that different dialkyl diselenides could react with a wide range of 1,7-diene to achieve seven-membered products in good to excellent yields. Furthermore, this synthesis was directed to obtain the desired target products, indicating that this approach has an excellent chemical selectivity.
View Article and Find Full Text PDFOrg Lett
September 2025
College of Chemistry and Materials Science, Key Laboratory of Chemical Biology of Hebei Province, Hebei University, Baoding, Hebei 071002, P. R. China.
Four novel coumarin-containing arenes bearing a [5]/[6]helicene unit (, , , and ) have been readily synthesized and structurally verified by X-ray crystallographic analysis. The chiral resolution of molecules , , and has enabled a detailed investigation of their chiroptical properties and the kinetics of enantiomerization, manifesting that the [6]helicenes and exhibit a more enhanced chiroptical response compared to [5]helicene .
View Article and Find Full Text PDFBioresour Technol
September 2025
School of Agricultural Engineering and Food Science, Shandong University of Technology, Zibo 255000, China; Zibo Engineering Research Center for Bio-based New Materials, Zibo 255000, China. Electronic address:
Tungsten disulfide (WS), a two-dimensional adsorbent material, has garnered great attention in removing lead ions (Pb) from water due to their extensive exposed adsorption sites. However, WS nanosheets inevitably agglomerated and stacked during the preparation and adsorption process, leading to reduced adsorption efficiency. Current method of enhancing WS dispersion is mainly blending with synthetic polymers, but these synthetic polymers themselves do not possess adsorption properties, resulting adsorption effect enhancement poorly.
View Article and Find Full Text PDFJ Colloid Interface Sci
September 2025
Faculty of Chemical Engineering, Kunming University of Science and Technology, Kunming 650093, China.
Encapsulation of non-noble bimetallic nanoparticles within a zeolite framework can improve the stability and accessibility of active sites, but the single microporous structure and poor metal stability decreased the catalytic performance of the catalyst. Here, 3D hierarchical ZSM-5 zeolite encapsulated NiCo nanoparticles (NiCo@3DHZ5) were synthesized by Bottom-up confined steam-assisted crystallization (SAC) one-pot hydrothermal method and applied to the hydrodeoxygenation of vanillin. A series of characterizations showed that highly stable alloyed NiCo nanoparticles were encapsulated in a framework of 3DHZ5, the strong metal-zeolite interactions resulted in highly dispersed NiCo nano-alloys facilitated hydrogen adsorption and spillover of active hydrogen atoms, and the 3D hierarchical structure promoted oxygenated substrate diffusion, the synergy interaction between the alloy particles confined in the 3DHZ5 pores and the acidic sites on the zeolite surface promoted the selective conversion of vanillin.
View Article and Find Full Text PDFJ Colloid Interface Sci
September 2025
College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, Qingdao 266042, PR China. Electronic address:
Transition metal fluorides because of the high electronegativity of fluorine may enhance the local electron density of the metal sites and promote water molecule dissociation and charge transfer. However, enhancing the intrinsic activity of fluorides to improve material stability remains a challenge. Herein, we develop an innovative four-step synthetic strategy (electrochemical deposition → co-precipitation → ligand exchange → in situ fluorination) to engineer three-dimensional porous Fe-doped CoF nanocubes vertically anchored on MXene (Fe-CoF/MXene/NF).
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