scholarly journals Self-Propulsion Enhances Polymerization

Entropy ◽  
2020 ◽  
Vol 22 (2) ◽  
pp. 251 ◽  
Author(s):  
Maximino Aldana ◽  
Miguel Fuentes-Cabrera ◽  
Martín Zumaya

Self-assembly is a spontaneous process through which macroscopic structures are formed from basic microscopic constituents (e.g., molecules or colloids). By contrast, the formation of large biological molecules inside the cell (such as proteins or nucleic acids) is a process more akin to self-organization than to self-assembly, as it requires a constant supply of external energy. Recent studies have tried to merge self-assembly with self-organization by analyzing the assembly of self-propelled (or active) colloid-like particles whose motion is driven by a permanent source of energy. Here we present evidence that points to the fact that self-propulsion considerably enhances the assembly of polymers: self-propelled molecules are found to assemble faster into polymer-like structures than non self-propelled ones. The average polymer length increases towards a maximum as the self-propulsion force increases. Beyond this maximum, the average polymer length decreases due to the competition between bonding energy and disruptive forces that result from collisions. The assembly of active molecules might have promoted the formation of large pre-biotic polymers that could be the precursors of the informational polymers we observe nowadays.

Author(s):  
Maximino Aldana ◽  
Miguel Fuentes-Cabrera ◽  
Martín Zumaya

Self-assembly is a spontaneous process through which macroscopic structures are formed from basic microscopic constituents (e.g. molecules or colloids). By contrast, the formation of large biological molecules inside the cell (such as proteins or nucleic acids) is a process more akin to self-organization than to self-assembly, as it requires a constant supply of external energy. Recent studies have tried to merge self-assembly with self-organization by analyzing the assembly of self-propelled (or active) colloid-like particles whose motion is driven by a permanent source of energy. Here we present evidence that points to the fact that self-propulsion considerably enhances the assembly of polymers: self-propelled molecules are found to assemble into polymer-like structures, the average length of which increases towards a maximum as the self-propulsion force increases. Beyond this maximum, the average polymer length decreases due to the competition between bonding energy and disruptive forces that result from collisions. The assembly of active molecules might have promoted the formation of large pre-biotic polymers that could be the precursors of the informational polymers we observe nowadays.


2021 ◽  
Vol 12 (1) ◽  
pp. 270-281
Author(s):  
Stefan Bitter ◽  
Moritz Schlötter ◽  
Markus Schilling ◽  
Marina Krumova ◽  
Sebastian Polarz ◽  
...  

The self-organization properties of a stimuli responsive amphiphile can be altered by subjecting the paramagnetic oxidized form to a magnetic field of 0.8 T and monitored in real time by coupling optical birefringence with dynamic light scattering.


Author(s):  
Alejandro Rodríguez ◽  
Alexander Grushin ◽  
James A. Reggia

Drawing inspiration from social interactions in nature, swarm intelligence has presented a promising approach to the design of complex systems consisting of numerous, simple parts, to solve a wide variety of problems. Swarm intelligence systems involve highly parallel computations across space, based heavily on the emergence of global behavior through local interactions of components. This has a disadvantage as the desired behavior of a system becomes hard to predict or design. Here we describe how to provide greater control over swarm intelligence systems, and potentially more useful goal-oriented behavior, by introducing hierarchical controllers in the components. This allows each particle-like controller to extend its reactive behavior in a more goal-oriented style, while keeping the locality of the interactions. We present three systems designed using this approach: a competitive foraging system, a system for the collective transport and distribution of goods, and a self-assembly system capable of creating complex 3D structures. Our results show that it is possible to guide the self-organization process at different levels of the designated task, suggesting that self-organizing behavior may be extensible to support problem solving in various contexts.


2007 ◽  
Vol 35 (3) ◽  
pp. 502-507 ◽  
Author(s):  
J.A.R. Worrall ◽  
M. Górna ◽  
X.Y. Pei ◽  
D.R. Spring ◽  
R.L. Nicholson ◽  
...  

The principles of self-assembly are described for naturally occurring macromolecules and for complex assemblies formed from simple synthetic constituents. Many biological molecules owe their function and specificity to their three-dimensional folds, and, in many cases, these folds are specified entirely by the sequence of the constituent amino acids or nucleic acids, and without the requirement for additional machinery to guide the formation of the structure. Thus sequence may often be sufficient to guide the assembly process, starting from denatured components having little or no folds, to the completion state with the stable, equilibrium fold that encompasses functional activity. Self-assembly of homopolymeric structures does not necessarily preserve symmetry, and some polymeric assemblies are organized so that their chemically identical subunits pack stably in geometrically non-equivalent ways. Self-assembly can also involve scaffolds that lack structure, as seen in the multi-enzyme assembly, the degradosome. The stable self-assembly of lipids into dynamic membraneous sheets is also described, and an example is shown in which a synthetic detergent can assemble into membrane layers.


RSC Advances ◽  
2017 ◽  
Vol 7 (25) ◽  
pp. 15337-15341 ◽  
Author(s):  
M. Facchin ◽  
A. Scarso ◽  
M. Selva ◽  
A. Perosa ◽  
P. Riello

Unconventional life forms based on membranes able to self-assemble in hydrocarbons instead of water might exist in the hydrocarbon-rich environment of Titan. We present evidence of the self-assembly of reverse surfactants to yield typical micelles in a hydrocarbon solvent.


Author(s):  
Анна Нориковна Адамян ◽  
Александра Ивановна Иванова ◽  
Елена Михайловна Семенова ◽  
Максим Дмитриевич Малышев ◽  
Светлана Дмитриевна Хижняк ◽  
...  

Комплексно исследовано влияние дневного освещения на процесс самоорганизации в цистеин-серебряном растворе (ЦСР) и гидрогелях на его основе. Установлено, что ЦСР на основе L-цистеина и ацетата серебра под действием освещения окрашивается сначала в желтый, а затем в коричневый цвет, что является следствием плазмонного резонанса на образующихся наночастицах серебра (НЧС) в ЦСР и гидрогелях. Предложена модель формирования НЧ в гидрогеле. The effect of daylight on the self-assembly process in cysteine-silver solution (CSS) and hydrogels based on it has been comprehensively studied. It was found that CSS based on L-cysteine and silver acetate under the action of illumination first turns yellow and then brown, which is a consequence of plasmon resonance on the resulting silver nanoparticles in CSS and hydrogels. A model for the formation of silver nanoparticles in a hydrogel is proposed.


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