scholarly journals Nanoscale elongating control of the self-assembled protein filament with the cysteine-introduced building blocks

2009 ◽  
Vol 18 (5) ◽  
pp. 960-969 ◽  
Author(s):  
Kengo Usui ◽  
Tei Maki ◽  
Fuyu Ito ◽  
Atsushi Suenaga ◽  
Satoru Kidoaki ◽  
...  
Soft Matter ◽  
2021 ◽  
Author(s):  
Jiawei Lu ◽  
Xiangyu Bu ◽  
Xinghua Zhang ◽  
Bing Liu

The shapes of colloidal particles are crucial to the self-assembled superstructures. Understanding the relationship between the shapes of building blocks and the resulting crystal structures is an important fundamental question....


Materials ◽  
2019 ◽  
Vol 12 (10) ◽  
pp. 1635 ◽  
Author(s):  
Hee-Jin Kim ◽  
Sungwoo Cho ◽  
Seung Joo Oh ◽  
Sung Gyu Shin ◽  
Hee Wook Ryu ◽  
...  

Hydrogels incorporated with hydrophobic motifs have received considerable attention to recapitulate the cellular microenvironments, specifically for the bio-mineralization of a 3D matrix. Introduction of hydrophobic molecules into a hydrogel often results in irregular arrangement of the motifs, and further phase separation of hydrophobic domains, but limited efforts have been made to resolve this challenge in developing the hydrophobically-modified hydrogel. Therefore, this study presents an advanced integrative strategy to incorporate hydrophobic domains regularly in a hydrogel using self-assembled domains formed with polymer cross-linkers, building blocks of a hydrogel. Self-assemblies formed by polymer cross-linkers were examined as micro-domains to incorporate hydrophobic motifs in a hydrogel. The self-assembled structures in a pre-gelled solution were confirmed with the fluorescence analysis and the hydrophobicity of a hydrogel could be tuned by incorporating the hydrophobic chains in a controlled manner. Overall, the results of this study would greatly serve to tuning performance of a wide array of hydrophobically-modified hydrogels in drug delivery, cell therapies and tissue engineering.


1997 ◽  
Vol 488 ◽  
Author(s):  
DeQuan Li ◽  
M. Lütt ◽  
Xiaobo Shi ◽  
M. R. Fitzsimmons

AbstractThe layer-by-layer growth of film structures consisting of sequential depositions of oppositely charged polymers and macrocycles (ring-shaped molecules) have been constructed using molecular self-assembly techniques. These self-assembled thin films were characterized with X-ray reflectometry, which yielded (1) the average electron density, (2) the average thicknesses, and (3) the roughness of the growth surface of the self-assembled multilayer of macrocycles and polymers. These observations suggest that inorganic-organic interactions play an important role during the initial stages of thin-film growth, but less so as the thin film becomes thicker. Optical absorption techniques were also used to characterize the self-assembled multilayers. Phorphyrin and phthalocyanine derivatives were chosen as the building blocks of the self-assembled multilayers because of their interesting optical properties.


2019 ◽  
Vol 2 (1) ◽  
Author(s):  
Leonardo Hayato Foianesi-Takeshige ◽  
Satoshi Takahashi ◽  
Tomoki Tateishi ◽  
Ryosuke Sekine ◽  
Atsushi Okazawa ◽  
...  

Abstract The template effect is a key feature to control the arrangement of building blocks in assemblies, but its kinetic nature remains elusive compared to the thermodynamic aspects, with the exception of very simple reactions. Here we report a kinetic template effect in a self-assembled cage composed of flexible ditopic ligands and Pd(II) ions. Without template anion, a micrometer-sized sheet is kinetically trapped (off-pathway), which is converted into the thermodynamically most stable cage by the template anion. When the template anion is present from the start, the cage is selectively produced by the preferential cyclization of a dinuclear intermediate (on-pathway). Quantitative and numerical analyses of the self-assembly of the cage on the on-pathway revealed that the accelerating effect of the template is stronger for the early stage reactions of the self-assembly than for the final cage formation step itself, indicating the kinetic template effect.


2009 ◽  
Vol 18 (7) ◽  
pp. 1571-1571
Author(s):  
Kengo Usui ◽  
Tei Maki ◽  
Fuyu Ito ◽  
Atsushi Suenaga ◽  
Satoru Kidoaki ◽  
...  

Polymers ◽  
2021 ◽  
Vol 13 (7) ◽  
pp. 1114
Author(s):  
Petra Bačová ◽  
Dimitris G. Mintis ◽  
Eirini Gkolfi ◽  
Vagelis Harmandaris

We present an atomistic molecular dynamics study of self-assembled mikto-arm stars, which resemble patchy-like particles. By increasing the number of stars in the system, we propose a systematic way of examining the mutual orientation of these fully penetrable patchy-like objects. The individual stars maintain their patchy-like morphology when creating a mesoscopic (macromolecular) self-assembled object of more than three stars. The self-assembly of mikto-arm stars does not lead to a deformation of the stars, and their shape remains spherical. We identified characteristic sub-units in the self-assembled structure, differing by the mutual orientation of the nearest neighbor stars. The current work aims to elucidate the possible arrangements of the realistic, fully penetrable patchy particles in polymer matrix and to serve as a model system for further studies of nanostructured materials or all-polymer nanocomposites using the mikto-arm stars as building blocks.


2019 ◽  
Author(s):  
Willy Klöckner ◽  
Cristian Patiño Vidal ◽  
Carol López de Dicastillo ◽  
Ram Manohar Yadav ◽  
D I N E S H P SINGH

Self-assembled 3D structures with 0, 1 or 2D nano building blocks are fascinating due to its astounding new and enhanced properties for various applications. Here we report the acetonitrile mediated synthesis of self-assembled bulk cylinder of length ~ 9.00 cm and diameter ~ 4.0 cm consolidated with ultralong and very thin silver vanadate nanowires and its enhanced antibacterial activity.  The addition of acetonitrile during synthesis and its volumetric concentration plays an important role in the self-assembly. The use of 30 mL acetonitrile during the mixing of the reactants AgNO3 and NH4VO3 and post hydrothermal treatment at 200 °C for 12 h result the formation of bulk cylinder like structure.  X-ray diffraction (XRD) and Scanning electron microscopy (SEM) revealed that the bulk cylinder is consolidated with ultrathin and long β-AgVO3 nanowires having minimum diameter ~16 nm and of undefined length (approximately 10 mm long). The self-assembled β-AgVO3nanowire like structure with very high surface area exhibited very high antibacterial activity against Listeria innocuaATCC 33090 and Staphylococcus aureusATCC 25923 and Escherichia coliATCC 25922, as Gram-positive and Gram-negative bacteria, respectively. 


2021 ◽  
Vol 12 ◽  
pp. 1140-1150
Author(s):  
Huan Ren ◽  
Lifang Wu ◽  
Lina Tan ◽  
Yanni Bao ◽  
Yuchen Ma ◽  
...  

Biomolecules, such as proteins and peptides, can be self-assembled. They are widely distributed, easy to obtain, and biocompatible. However, the self-assembly of proteins and peptides has disadvantages, such as difficulty in obtaining high quantities of materials, high cost, polydispersity, and purification limitations. The difficulties in using proteins and peptides as functional materials make it more complicate to arrange assembled nanostructures at both microscopic and macroscopic scales. Amino acids, as the smallest constituent of proteins and the smallest constituent in the bottom-up approach, are the smallest building blocks that can be self-assembled. The self-assembly of single amino acids has the advantages of low synthesis cost, simple modeling, excellent biocompatibility and biodegradability in vivo. In addition, amino acids can be assembled with other components to meet multiple scientific needs. However, using these simple building blocks to design attractive materials remains a challenge due to the simplicity of the amino acids. Most of the review articles about self-assembly focus on large molecules, such as peptides and proteins. The preparation of complicated materials by self-assembly of amino acids has not yet been evaluated. Therefore, it is of great significance to systematically summarize the literature of amino acid self-assembly. This article reviews the recent advances in amino acid self-assembly regarding amino acid self-assembly, functional amino acid self-assembly, amino acid coordination self-assembly, and amino acid regulatory functional molecule self-assembly.


Molecules ◽  
2020 ◽  
Vol 25 (2) ◽  
pp. 402
Author(s):  
Changjun Park ◽  
Jinhee Lee ◽  
Taehyoung Kim ◽  
Jaechang Lim ◽  
Jeyoung Park ◽  
...  

Here, we report the formation of homochiral supramolecular thin film from achiral molecules, by using circularly polarized light (CPL) only as a chiral source, on the condition that irradiation of CPL does not induce a photochemical change of the achiral molecules. Thin films of self-assembled structures consisting of chiral supramolecular fibrils was obtained from the triarylamine derivatives through evaporation of the self-assembled triarylamine solution. The homochiral supramolecular helices with the desired handedness was achieved by irradiation of circularly polarized visible light during the self-assembly process, and the chiral stability of supramolecular self-assembled product was achieved by photopolymerization of the diacetylene moieties at side chains of the building blocks, with irradiation of circularly polarized ultraviolet light. This work provides a novel methodology for the generation of homochiral supramolecular thin film from the corresponding achiral molecules.


2016 ◽  
Vol 52 (28) ◽  
pp. 5023-5026 ◽  
Author(s):  
Lin-Xiu Dai ◽  
Xin-Yu Wang ◽  
Xiao-Yu Zheng ◽  
Ya-Wen Zhang

N,N-Dimethylformamide (DMF) serves as the facet-specific agent for the formation of a cubic shape and the structure-directing agent for the self-assembly of Pt and Pt–Rh building blocks of the supercrystals.


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