Nanostructure and amphiphile self-assembly in polar molecular solvents: amides and the “solvophobic effect”

2011 ◽  
Vol 13 (20) ◽  
pp. 9180 ◽  
Author(s):  
Tamar L. Greaves ◽  
Asoka Weerawardena ◽  
Calum J. Drummond
Keyword(s):  
Self Assembly ◽  
Solvophobic Effect ◽  
Molecular Solvents

Activity and conformation of lysozyme in molecular solvents, protic ionic liquids (PILs) and salt–water systems

2016 ◽  
Vol 18 (37) ◽  
pp. 25926-25936 ◽  
Author(s):  
Emmy C. Wijaya ◽  
Frances Separovic ◽  
Calum J. Drummond ◽  
Tamar L. Greaves
Keyword(s):  
Electrostatic Interactions ◽  
Enzyme Stability ◽  
Salt Water ◽  
Water Systems ◽  
Salt Solutions ◽  
Protic Ionic Liquids ◽  
Solvophobic Effect ◽  
Molecular Solvents ◽  
Role Of Solvent

The role of solvent features on enzyme stability was investigated by comparing the conformation and activity of lysozyme in molecular solvents, PILs and salt solutions. Electrostatic interactions and the solvophobic effect dominated at low and high solvent concentrations, respectively.

Enhanced self-assembly for the solubilization of cholesterol in molecular solvent/ionic liquid mixtures

2017 ◽  
Vol 19 (17) ◽  
pp. 10835-10842 ◽  
Author(s):  
Wenbin Jin ◽  
Yuqi Ke ◽  
Xianxian Liu ◽  
Qiwei Yang ◽  
Zongbi Bao ◽  
...  
Keyword(s):  
Ionic Liquid ◽  
Synergistic Effect ◽  
Self Assembly ◽  
Liquid Mixtures ◽  
Molecular Solvents

Enhanced solute–solvent self-assembly arising from a synergistic effect between LCC-ILs and molecular solvents enables unprecedented solubility of sparingly soluble cholesterol.

Effect of molecular solvents of varying polarity on the self-assembly of 1-n-dodecyl-3-methylimidazolium octylsulfate ionic liquid

2018 ◽  
Vol 17 (03) ◽  
pp. 1840004 ◽  
Author(s):  
Utkarsh Kapoor ◽  
Jindal K. Shah
Keyword(s):  
Ionic Liquid ◽  
Self Assembly ◽  
Large Scale ◽  
Structural Features ◽  
Nematic Order ◽  
Structure Factors ◽  
Dynamics Simulations ◽  
Multiple Domains ◽  
Molecular Solvents

Large-scale molecular dynamics simulations consisting of more than 88,000–106,000 atoms for approximately 250 ns (including equilibration and production) were conducted to assess the effect of polar, nonpolar and amphiphilic molecular solvents on the nanoscale structuring of 1-[Formula: see text]-dodecyl-3-methylimidazolium [C[Formula: see text]mim] octylsulfate [C8SO4] ionic liquid (IL). Water [H2O], [Formula: see text]-octane [C8H[Formula: see text]] and 1-octanol [C8H[Formula: see text]OH] are employed as examples of polar, nonpolar, and amphiphilic molecules, respectively. The results indicate that each of these molecular solvents modify the nanosegregation behavior of the ionic liquid in a unique way. Water induces a high order of structuring of the ionic liquid as indicated by extremely high nematic order parameter for the system. In addition, the morphology of the neat ionic liquid is transformed from layer-like to that of bilayer-like in which the polar and nonpolar domains alternate. The presence of water also causes the stretching of the nonpolar domain, thus, increasing its size. At the concentration examined in this work, [Formula: see text]-octane is found to be only partially miscible with the ionic liquid. The polar network is maintained; however, the continuous cationic nonpolar domain is split into multiple domains. [Formula: see text]-octane is accommodated in the ionic liquid nonpolar domain. Similarly, the amphiphilicity of 1-octanol leads to an increase in the number of cationic as well as anionic domains. The overall nonpolar domain length, however, remains nearly identical to that found for the pure ionic liquid. Additional characterization of structural features of the three systems is discussed in terms of one-dimensional number densities, nematic order parameters for the overall systems and their components and structure factors.

In vitro and in vivo polysaccharides assembly: ultrastructural and cytochemical study of growing plant cell wall components.

1978 ◽  
Vol 36 (2) ◽  
pp. 434-435
Author(s):  
D. Reis ◽  
B. Vian ◽  
J. C. Roland
Keyword(s):  
Cell Wall ◽  
Self Assembly ◽  
Plant Cell Wall ◽  
Higher Plants ◽  
Three Dimensional ◽  
Cytochemical Study ◽  
Wall Components

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.

The Nature of Rapidly Extracted Phycocyanin from the Blue-Green Alga Plectonema Boryanum

1971 ◽  
Vol 29 ◽  
pp. 366-367
Author(s):  
M. Kessel ◽  
R. MacColl
Keyword(s):  
Self Assembly ◽  
Analytical Ultracentrifugation ◽  
Uranyl Acetate ◽  
The Self ◽  
Major Protein ◽  
Subunit Structure ◽  
Blue Green Alga ◽  
Thin Sections ◽  
Blue Green Algae ◽  
Cacodylate Buffer

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.

Video real-time imaging of artificial membranes during freeze-drying by cryo-electron microscopy

1988 ◽  
Vol 46 ◽  
pp. 16-17
Author(s):  
Alan S. Rudolph ◽  
Ronald R. Price
Keyword(s):  
Real Time ◽  
Self Assembly ◽  
Freeze Drying ◽  
Video Capture ◽  
Drying Process ◽  
Artificial Membranes ◽  
The Past ◽  
Cryo Electron Microscopy ◽  
Spherical Structures ◽  
Capture Techniques

We have employed cryoelectron microscopy to visualize events that occur during the freeze-drying of artificial membranes by employing real time video capture techniques. Artificial membranes or liposomes which are spherical structures within internal aqueous space are stabilized by water which provides the driving force for spontaneous self-assembly of these structures. Previous assays of damage to these structures which are induced by freeze drying reveal that the two principal deleterious events that occur are 1) fusion of liposomes and 2) leakage of contents trapped within the liposome [1]. In the past the only way to access these events was to examine the liposomes following the dehydration event. This technique allows the event to be monitored in real time as the liposomes destabilize and as water is sublimed at cryo temperatures in the vacuum of the microscope. The method by which liposomes are compromised by freeze-drying are largely unknown. This technique has shown that cryo-protectants such as glycerol and carbohydrates are able to maintain liposomal structure throughout the drying process.

Biomimetic materials: An introduction

1992 ◽  
Vol 50 (2) ◽  
pp. 1020-1021 ◽  
Author(s):  
M. Sarikaya ◽  
J. T. Staley ◽  
I. A. Aksay
Keyword(s):  
Self Assembly ◽  
Structural Control ◽  
Hierarchical Structures ◽  
Ceramic Composites ◽  
Advanced Materials ◽  
Length Scale ◽  
Spider Webs ◽  
Biomimetic Materials ◽  
Synthetic Materials ◽  
All Ceramic

Biomimetics is an area of research in which the analysis of structures and functions of natural materials provide a source of inspiration for design and processing concepts for novel synthetic materials. Through biomimetics, it may be possible to establish structural control on a continuous length scale, resulting in superior structures able to withstand the requirements placed upon advanced materials. It is well recognized that biological systems efficiently produce complex and hierarchical structures on the molecular, micrometer, and macro scales with unique properties, and with greater structural control than is possible with synthetic materials. The dynamism of these systems allows the collection and transport of constituents; the nucleation, configuration, and growth of new structures by self-assembly; and the repair and replacement of old and damaged components. These materials include all-organic components such as spider webs and insect cuticles (Fig. 1); inorganic-organic composites, such as seashells (Fig. 2) and bones; all-ceramic composites, such as sea urchin teeth, spines, and other skeletal units (Fig. 3); and inorganic ultrafine magnetic and semiconducting particles produced by bacteria and algae, respectively (Fig. 4).

Interrelationship of the cellular distribution and secretion of regular structure (RS) protein in Bacillus licheniformis nm 105

1992 ◽  
Vol 50 (1) ◽  
pp. 712-713
Author(s):  
Xiaorong Zhu ◽  
Richard McVeigh ◽  
Bijan K. Ghosh
Keyword(s):  
Alkaline Phosphatase ◽  
Bacillus Licheniformis ◽  
Self Assembly ◽  
Gel Electrophoresis ◽  
Culture Supernatant ◽  
Regular Structure ◽  
The Self ◽  
Cellular Distribution ◽  
Structural Protein ◽  
Laboratory Cultures

A mutant of Bacillus licheniformis 749/C, NM 105 exhibits some notable properties, e.g., arrest of alkaline phosphatase secretion and overexpression and hypersecretion of RS protein. Although RS is known to be widely distributed in many microbes, it is rarely found, with a few exceptions, in laboratory cultures of microorganisms. RS protein is a structural protein and has the unusual properties to form aggregate. This characteristic may have been responsible for the self assembly of RS into regular tetragonal structures. Another uncommon characteristic of RS is that enhanced synthesis and secretion which occurs when the cells cease to grow. Assembled RS protein with a tetragonal structure is not seen inside cells at any stage of cell growth including cells in the stationary phase of growth. Gel electrophoresis of the culture supernatant shows a very large amount of RS protein in the stationary culture of the B. licheniformis. It seems, Therefore, that the RS protein is cotranslationally secreted and self assembled on the envelope surface.

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