scholarly journals Design strategies for self-assembly of discrete targets

2015 ◽  
Vol 143 (4) ◽  
pp. 044905 ◽  
Author(s):  
Jim Madge ◽  
Mark A. Miller
Author(s):  
Nian Lin ◽  
Sebastian Stepanow

This article describes the use of supramolecular chemistry to design low-dimensional nanostructures at surfaces. In particular, it discusses the design strategies of two types of low-dimensional supramolecular nanostructures: structures stabilized by hydrogen bonds and structures stabilized by metal-ligand co-ordination interactions. After providing an overview of hydrogen-bond systems such as 0D discrete clusters, 1D chains, and 2D open networks and close-packed arrays, the article considers metal-co-ordination systems. It also presents experimental results showing that both hydrogen bonds and metal co-ordination offer protocols to achieve unique nanostructured systems on 2D surfaces or interfaces. Noting that the conventional 3D supramolecular self-assembly has generated a vast number of nanostructures revealing high complexity and functionality, the article suggests that 2D approaches can be applied to substrates with different symmetries as well as physical and chemical properties.


2019 ◽  
Vol 21 (2) ◽  
pp. 670-679 ◽  
Author(s):  
Tan Hu ◽  
Zhuo Zhang ◽  
Hao Hu ◽  
Stephen Robert Euston ◽  
Siyi Pan

2010 ◽  
Vol 82 (3) ◽  
pp. 523-533 ◽  
Author(s):  
Emilio M. Pérez ◽  
Nazario Martín

The search for molecular receptors capable of forming stable associates with fullerenes is a very active field of research in fullerene chemistry, with the purification from fullerite and the self-assembly of nanoscale electronic devices as driving forces. The construction of bivalent, tweezer-like receptors featuring two recognizing units connected through a spacer is one of the most successful design strategies employed in this field. Here, we present an overview of the most significant examples of these “molecular tweezers” for fullerenes.


2016 ◽  
Vol 52 (93) ◽  
pp. 13543-13555 ◽  
Author(s):  
Lizhi Zhao ◽  
Rui Qu ◽  
Ang Li ◽  
Rujiang Ma ◽  
Linqi Shi

This review covers recent research on design strategies for the cooperative self-assembly of porphyrins with polymers and its implementation as bioactive assembly.


2021 ◽  
Author(s):  
Pezhman Mohammadi ◽  
Julie-Anne Gandier ◽  
Nonappa Nonappa ◽  
Wolfgang Wagermaier ◽  
Ali Miserez ◽  
...  

Abstract Nature provides unique insights into design strategies evolved by living organisms to construct robust materials with a combination of mechanical properties that are challenging to replicate synthetically. Hereby, inspired by the impact-resistant dactyl club of the stomatopod, we rationally designed and produced a mineralized biocomposite in the complex-shapes of dental implant crowns exhibiting high strength, stiffness, and fracture toughness. This material consists of an expanded helicoidal organization of cellulose nano-crystals (CNCs) mixed with genetically-engineered proteins that regulate both binding to CNCs, as well as in situ growth of reinforcing apatite crystals. Critically, the structural properties emerge from controlled self-assembly across multiple length scales regulated by rational engineering and phase separation of the protein components. This work replicates multiscale biomanufacturing of a model biological material and also offers an innovative platform to synthesize multi-functional biocomposites whose properties can be finely regulated by colloidal self-assembly and engineering of its constitutive protein building blocks.


Molecules ◽  
2020 ◽  
Vol 25 (23) ◽  
pp. 5466
Author(s):  
Andreas Jaekel ◽  
Pascal Lill ◽  
Stephen Whitelam ◽  
Barbara Saccà

Since the pioneering work of Ned Seeman in the early 1980s, the use of the DNA molecule as a construction material experienced a rapid growth and led to the establishment of a new field of science, nowadays called structural DNA nanotechnology. Here, the self-recognition properties of DNA are employed to build micrometer-large molecular objects with nanometer-sized features, thus bridging the nano- to the microscopic world in a programmable fashion. Distinct design strategies and experimental procedures have been developed over the years, enabling the realization of extremely sophisticated structures with a level of control that approaches that of natural macromolecular assemblies. Nevertheless, our understanding of the building process, i.e., what defines the route that goes from the initial mixture of DNA strands to the final intertwined superstructure, is, in some cases, still limited. In this review, we describe the main structural and energetic features of DNA nanoconstructs, from the simple Holliday junction to more complicated DNA architectures, and present the theoretical frameworks that have been formulated until now to explain their self-assembly. Deeper insights into the underlying principles of DNA self-assembly may certainly help us to overcome current experimental challenges and foster the development of original strategies inspired to dissipative and evolutive assembly processes occurring in nature.


Pharmaceutics ◽  
2021 ◽  
Vol 13 (5) ◽  
pp. 753
Author(s):  
Tian-Tian Wang ◽  
Yi-Yi Xia ◽  
Jian-Qing Gao ◽  
Dong-Hang Xu ◽  
Min Han

Inspired by molecular self-assembly, which is ubiquitous in natural environments and biological systems, self-assembled peptides have become a research hotspot in the biomedical field due to their inherent biocompatibility and biodegradability, properties that are afforded by the amide linkages forming the peptide backbone. This review summarizes the biological advantages, principles, and design strategies of self-assembled polypeptide systems. We then focus on the latest advances in in situ self-assembly of polypeptides in medical applications, such as oncotherapy, materials science, regenerative medicine, and drug delivery, and then briefly discuss their potential challenges in clinical treatment.


Author(s):  
D. Reis ◽  
B. Vian ◽  
J. C. Roland

Wall morphogenesis in higher plants is a problem still open to controversy. Until now the possibility of a transmembrane control and the involvement of microtubules were mostly envisaged. Self-assembly processes have been observed in the case of walls of Chlamydomonas and bacteria. Spontaneous gelling interactions between xanthan and galactomannan from Ceratonia have been analyzed very recently. The present work provides indications that some processes of spontaneous aggregation could occur in higher plants during the formation and expansion of cell wall.Observations were performed on hypocotyl of mung bean (Phaseolus aureus) for which growth characteristics and wall composition have been previously defined.In situ, the walls of actively growing cells (primary walls) show an ordered three-dimensional organization (fig. 1). The wall is typically polylamellate with multifibrillar layers alternately transverse and longitudinal. Between these layers intermediate strata exist in which the orientation of microfibrils progressively rotates. Thus a progressive change in the morphogenetic activity occurs.


Author(s):  
M. Kessel ◽  
R. MacColl

The major protein of the blue-green algae is the biliprotein, C-phycocyanin (Amax = 620 nm), which is presumed to exist in the cell in the form of distinct aggregates called phycobilisomes. The self-assembly of C-phycocyanin from monomer to hexamer has been extensively studied, but the proposed next step in the assembly of a phycobilisome, the formation of 19s subunits, is completely unknown. We have used electron microscopy and analytical ultracentrifugation in combination with a method for rapid and gentle extraction of phycocyanin to study its subunit structure and assembly.To establish the existence of phycobilisomes, cells of P. boryanum in the log phase of growth, growing at a light intensity of 200 foot candles, were fixed in 2% glutaraldehyde in 0.1M cacodylate buffer, pH 7.0, for 3 hours at 4°C. The cells were post-fixed in 1% OsO4 in the same buffer overnight. Material was stained for 1 hour in uranyl acetate (1%), dehydrated and embedded in araldite and examined in thin sections.


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