scholarly journals Multi-Antigenic Virus-like Particle of SARS CoV-2 produced in Saccharomyces cerevisiae as a vaccine candidate

2020 ◽  
Author(s):  
Kajal Arora ◽  
Ruchir Rastogi ◽  
Nupur Mehrotra Arora ◽  
Deepak Parashar ◽  
Jeny Paliwal ◽  
...  
Keyword(s):  
Saccharomyces Cerevisiae ◽  
Self Assembly ◽  
Vaccine Candidate ◽  
Analytical Data ◽  
Surface Coat ◽  
Uniform Size ◽  
Virus Surface ◽  
Transmission Electron ◽  
Virus Like Particle ◽  
Uniform Size Distribution

AbstractSpike, Envelope and Membrane proteins from the SARS CoV-2 virus surface coat are important vaccine targets. We hereby report recombinant co-expression of the three proteins (Spike, Envelope and Membrane) in a engineered Saccharomyces cerevisiae platform (D-Crypt™) and their self-assembly as Virus-like particle (VLP). This design as a multi-antigenic VLP for SARS CoV-2 has the potential to be a scalable vaccine candidate. The VLP is confirmed by transmission electron microscopy (TEM) images of the SARS CoV-2, along with supportive HPLC, Dynamic Light Scattering (DLS) and allied analytical data. The images clearly outline the presence of a “Corona” like morphology, and uniform size distribution.

scholarly journals Influence of hematite nanorods on the mechanical properties of epoxy resin

2017 ◽  
Vol 82 (4) ◽  
pp. 437-447 ◽  
Author(s):  
Gordana Bogdanovic ◽  
Tijana Kovac ◽  
Enis Dzunuzovic ◽  
Milena Spírková ◽  
Phillip Ahrenkiel ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Epoxy Resin ◽  
Microstructural Characterization ◽  
Uniform Size ◽  
Force Microscopy ◽  
Atomic Force ◽  
Transmission Electron ◽  
Uniform Size Distribution ◽  
Tensile Toughness

The mechanical properties of nanocomposites obtained by incorporation of fairly uniform hematite nanorods (?-Fe2O3 NRs) into epoxy resin were studied as a function of the content of the inorganic phase. A thorough microstructural characterization of the ?-Fe2O3 NRs and the nanocomposites was performed using transmission electron microscopy (TEM) and atomic force microscopy (AFM). The TEM measurements revealed rod-like morphology of the nanofiller with a uniform size distribution (8.5 nm?170 nm, diameter?length). High-magnification TEM and AFM measurements indicated agglomeration of ?-Fe2O3 NRs embedded in the epoxy resin. Stress at break, strain at break, elastic modulus and tensile toughness of the nanocomposites were compared with the data obtained for pure epoxy resin. Significant influence of nanofiller on the mechanical properties of epoxy resin, as well as on the glass transition temperature, could be noticed for samples with low contents of the inorganic phase (up to 1 wt. %).

Wüstite nanocrystals: Synthesis, structure and superlattice formation

2007 ◽  
Vol 22 (7) ◽  
pp. 1987-1995 ◽  
Author(s):  
Ming Yin ◽  
Zhuoying Chen ◽  
Brian Deegan ◽  
Stephen O’Brien
Keyword(s):  
Self Assembly ◽  
Three Dimensional ◽  
Size Control ◽  
Molar Ratio ◽  
X Ray Diffraction ◽  
Salt Crystal ◽  
Uniform Size ◽  
Nonpolar Solvents ◽  
Transmission Electron ◽  
State Kinetic

Monodisperse ligand-capped cubic wüstite FexO nanocrystals were prepared by a novel thermal decomposition method of iron (II) acetate in the presence of oleic acid as the surfactant. Controlled size distributions of cubic nanoparticles possessing the rock salt crystal structure were isolated in the range 10–18 nm. The influence of molar ratio of surfactant to precursor was investigated to understand size control and monodispersity. Using inexpensive, nontoxic metal salts as reactants, we were able to synthesize gram-scale quantities of relatively monodisperse nanocrystals in a single reaction, without further size selection, characterized by x-ray diffraction and transmission electron microscopy. The procedure enables the collection of samples of uniform size as a function of time, thus permitting a preliminary solid-state kinetic analysis of the reaction as a function of increasing particle size. Following controlled evaporation from nonpolar solvents, self-assembly into two-dimensional arrays, three-dimensional single-component superlattices, and binary superlattices with gold nanoparticles were observed and characterized.

PREPARATION OF MnO2 NANOPARTICLES BY A SOLUTION BASED APPROACH FOR ELECTROCHEMICAL CAPACITOR

2020 ◽  
Vol 27 (08) ◽  
pp. 1950199 ◽  
Author(s):  
ANKUR SOAM ◽  
RAHUL KUMAR
Keyword(s):  
Electrochemical Capacitor ◽  
X Ray Diffraction ◽  
Uniform Size ◽  
X Ray ◽  
Supercapacitor Application ◽  
Energy Storage Application ◽  
Transmission Electron ◽  
Mno2 Nanoparticles ◽  
Scan Rate ◽  
Uniform Size Distribution

We report here the development of MnO2 nanostructure electrode for electrochemical energy storage application. MnO2 nanoparticles synthesized by a facile and efficient precipitation approach have been investigated for supercapacitor application. The structures and morphologies of MnO2 nanoparticles were systematically studied using X-ray diffraction, Raman spectroscopy and transmission electron microscopy. The synthesized nanoparticles are observed spherical in shape with uniform size distribution. The electrochemical properties were studied in two-electrode configuration by cyclic voltammetry process. A specific capacitance of 52.8[Formula: see text]F/g has been obtained for MnO2 nanoparticles at scan rate of 100[Formula: see text]mV/s. The electrode is able to deliver a power density of 0.66[Formula: see text]kW/kg and energy density of 1.8[Formula: see text]Wh/kg.

Bottom-up Evolution from Disks to High-Genus Polymersomes

2018 ◽  
Author(s):  
Claudia Contini ◽  
Russell Pearson ◽  
Linge Wang ◽  
Lea Messager ◽  
Jens Gaitzsch ◽  
...  
Keyword(s):  
Self Assembly ◽  
The Self ◽  
Amphiphilic Copolymers ◽  
Chain Entanglement ◽  
Bottom Up ◽  
New Approach ◽  
High Genus ◽  
Transmission Electron ◽  
Minimal Radius ◽  
Stop Flow

<div><div><div><p>We report the design of polymersomes using a bottom-up approach where the self-assembly of amphiphilic copolymers poly(2-(methacryloyloxy) ethyl phosphorylcholine)–poly(2-(diisopropylamino) ethyl methacrylate) (PMPC-PDPA) into membranes is tuned using pH and temperature. We study this process in detail using transmission electron microscopy (TEM), nuclear magnetic resonance (NMR) spectroscopy, dynamic light scattering (DLS), and stop-flow ab- sorbance disclosing the molecular and supramolecular anatomy of each structure observed. We report a clear evolution from disk micelles to vesicle to high-genus vesicles where each passage is controlled by pH switch or temperature. We show that the process can be rationalised adapting membrane physics theories disclosing important scaling principles that allow the estimation of the vesiculation minimal radius as well as chain entanglement and coupling. This allows us to propose a new approach to generate nanoscale vesicles with genus from 0 to 70 which have been very elusive and difficult to control so far.</p></div></div></div>

Bottom-up Evolution from Disks to High-Genus Polymersomes

2018 ◽  
Author(s):  
Claudia Contini ◽  
Russell Pearson ◽  
Linge Wang ◽  
Lea Messager ◽  
Jens Gaitzsch ◽  
...  
Keyword(s):  
Self Assembly ◽  
The Self ◽  
Amphiphilic Copolymers ◽  
Chain Entanglement ◽  
Bottom Up ◽  
New Approach ◽  
High Genus ◽  
Transmission Electron ◽  
Minimal Radius ◽  
Stop Flow

<div><div><div><p>We report the design of polymersomes using a bottom-up approach where the self-assembly of amphiphilic copolymers poly(2-(methacryloyloxy) ethyl phosphorylcholine)–poly(2-(diisopropylamino) ethyl methacrylate) (PMPC-PDPA) into membranes is tuned using pH and temperature. We study this process in detail using transmission electron microscopy (TEM), nuclear magnetic resonance (NMR) spectroscopy, dynamic light scattering (DLS), and stop-flow ab- sorbance disclosing the molecular and supramolecular anatomy of each structure observed. We report a clear evolution from disk micelles to vesicle to high-genus vesicles where each passage is controlled by pH switch or temperature. We show that the process can be rationalised adapting membrane physics theories disclosing important scaling principles that allow the estimation of the vesiculation minimal radius as well as chain entanglement and coupling. This allows us to propose a new approach to generate nanoscale vesicles with genus from 0 to 70 which have been very elusive and difficult to control so far.</p></div></div></div>

scholarly journals Alpha helical surfactant-like peptides self-assemble into pH-dependent nanostructures

Soft Matter ◽  
2021 ◽  
Vol 17 (11) ◽  
pp. 3096-3104
Author(s):  
Valeria Castelletto ◽  
Jani Seitsonen ◽  
Janne Ruokolainen ◽  
Ian W. Hamley
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Small Angle ◽  
Self Assembly ◽  
X Ray ◽  
Cryogenic Transmission Electron Microscopy ◽  
X Ray Scattering ◽  
Transmission Electron ◽  
Ph Dependent ◽  
Ray Scattering

A designed surfactant-like peptide is shown, using a combination of cryogenic-transmission electron microscopy and small-angle X-ray scattering, to have remarkable pH-dependent self-assembly properties.

Self Assembling Nanostructured Delivery Vehicles for Biochemically Reactive Pairs

1994 ◽  
Vol 351 ◽  
Author(s):  
Nir Kossovsky ◽  
A. Gelman ◽  
H.J. Hnatyszyn ◽  
E. Sponsler ◽  
G.-M. Chow
Keyword(s):  
Physical Properties ◽  
Self Assembly ◽  
Materials Science ◽  
Technology Development ◽  
Biological Behavior ◽  
X Ray Diffraction ◽  
Self Assembling ◽  
Transmission Electron ◽  
Carbon Ceramic

ABSTRACTIntrigued by the deceptive simplicity and beauty of macromolecular self-assembly, our laboratory began studying models of self-assembly using solids, glasses, and colloidal substrates. These studies have defined a fundamental new colloidal material for supporting members of a biochemically reactive pair.The technology, a molecular transportation assembly, is based on preformed carbon ceramic nanoparticles and self assembled calcium-phosphate dihydrate particles to which glassy carbohydrates are then applied as a nanometer thick surface coating. This carbohydrate coated core functions as a dehydroprotectant and stabilizes surface immobilized members of a biochemically reactive pair. The final product, therefore, consists of three layers. The core is comprised of the ceramic, the second layer is the dehydroprotectant carbohydrate adhesive, and the surface layer is the biochemically reactive molecule for which delivery is desired.We have characterized many of the physical properties of this system and have evaluated the utility of this delivery technology in vitro and in animal models. Physical characterization has included standard and high resolution transmission electron microscopy, electron and x-ray diffraction and ζ potential analysis. Functional assays of the ability of the system to act as a nanoscale dehydroprotecting delivery vehicle have been performed on viral antigens, hemoglobin, and insulin. By all measures at present, the favorable physical properties and biological behavior of the molecular transportation assembly point to an exciting new interdisciplinary area of technology development in materials science, chemistry and biology.

Solvothermal Synthesis of Bi2Se3 Hexagonal Nanosheet Crystals

2011 ◽  
Vol 236-238 ◽  
pp. 1712-1716 ◽  
Author(s):  
Hai Tao Liu ◽  
Jun Dai ◽  
Jia Jia Zhang ◽  
Wei Dong Xiang
Keyword(s):  
Electron Microscope ◽  
Solvothermal Synthesis ◽  
Solvothermal Method ◽  
Raw Materials ◽  
X Ray Diffraction ◽  
Uniform Size ◽  
X Ray ◽  
Selected Area Electron Diffraction ◽  
Transmission Electron ◽  
Scanning Electron

Bismuth selenide (Bi2Se3) hexagonal nanosheet crystals with uniform size were successfully prepared via a solvothermal method at 160°C for 22 h using bismuth trichloride(BiCl3) and selenium powder(Se) as raw materials, sodium bisulfite(NaHSO3) as a reducing agent, diethylene glycol(DEG) as solvent, and ammonia as pH regulator. Various techniques such as X-ray diffraction (XRD), field-emission scanning electron microscope (FESEM), high-resolution transmission electron microscope (HRTEM), and selected area electron diffraction (SAED) were used to characterize the obtained products. Results show that the as-synthesized samples are pure Bi2Se3 hexagonal nanosheet crystals. A possible growth mechanism for Bi2Se3 hexagonal nanosheet crystals is also discussed based on the experiment.

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