Packaging of gold particles in viral capsids

In-vitro self-assembly conditions known to result in generating infectious virions have been used in vitro to reassemble bromovirus capsid proteins around negatively charged gold nanoparticles cores. We discuss here the optical properties (elastic light scattering) and the influence of the core size and of the functional moiety on the resulting virus-like particles. Our results indicate that the formation of a closed shell, as opposed to an amorphous protein coat, does occur and that the shell/core interactions can be tuned using different coatings on the nanoparticle core. Such studies may lead to real-time monitoring of viral traffic on the scale of a single virus, as well as to the possibility of chemical sensing along the intracellular and intercellular viral pathways and contribute to a better understanding of the virus transport and cellular compartmentalization.     

Selective Patterning of Gold Surfaces by Core/Shell,Semisoft Hybrid Nanoparticles

The generation of patterned surfaces with well‐defined nano‐ and microdomains is demonstrated by attaching core/shell, semisoft nanoparticles with narrow size distribution to microdomains of a gold‐coated silicon wafer. Near monodisperse nanoparticles are prepared using reversible addition‐fragmentation chain transfer (RAFT) polymerization, initiated from a silica surface, to prepare a polystyrene shell around a silica core. The particles are then used as‐prepared, or after aminolysis of the terminal thiocarbonyl group of the polystyrene shell, to give thiol‐terminated nanoparticles. When gold‐coated silicon wafers are immersed into very dilute suspensions of these particles (as low as 0.004 wt%), both types of particles are shown to adhere to the gold domains. The thiolated particles adhere selectively to the gold microdomains, allowing for microdomain patterning, while particles that contain the trithiocarbonate functionality lead to a much more even coverage of the gold surface with fewer particle aggregations.     

Viral Coat Proteins as Flexible Nano‐Building‐Blocks for Nanoparticle Encapsulation

Viral capsid–nanoparticle hybrid structures offer new opportunities for nanobiotechnology. We previously generated virus‐based nanoparticles (VNPs) of simian virus 40 (SV40) containing quantum dots (QDs) for cellular imaging. However, as an interesting issue of nano‐bio interfaces, the mechanism of nanoparticle (NP) encapsulation by viral coat proteins remains unclear. Here, four kinds of QDs with the same core/shell but different surface coatings are tested for encapsulation. All the QDs can be encapsulated efficiently and there is no correlation between the encapsulation efficiency and the surface charge of the QDs. All the SV40 VNPs encapsulating differently modified QDs show similar structures, fluorescence properties, and activity in entering living cells. These results demonstrate the flexibility of SV40 major capsid protein VP1 in NP encapsulation and provide new clues to the mechanism of NP packaging by viral shells.     

Versatile gradients of chemistry, bound ligands and nanoparticles on alumina nanopore arrays

Nanoporous alumina (PA) arrays produced by self-ordering growth, using electrochemical anodization, have been extensively explored for potential applications based upon the unique thermal, mechanical and structural properties, and high surface-to-volume ratio of these materials. However, the potential applications and functionality of these materials may be further extended by molecular-level engineering of the surface of the pore rims. In this paper we present a method for the generation of chemical gradients on the surface of PA arrays based upon plasma co-polymerization of two monomers. We further extend these chemical gradients, which are also gradients of surface charge, to those of bound ligands and number density gradients of nanoparticles. The latter represent a highly exotic new class of materials, comprising aligned PA, capped by gold nanoparticles around the rim of the pores. Gradients of chemistry, ligands and nanoparticles generated by our method retain the porous structure of the substrate, which is important in applications that take advantage of the inherent properties of these materials. This method can be readily extended to other porous materials.     

Nanoparticle-templated assembly of viral protein cages

Self-assembly of regular protein surfaces around nanoparticle templates provides a new class of hybrid biomaterials with potential applications in medical imaging and in bioanalytical sensing. We report here the first example of efficiently self-assembled virus-like particles (VLPs) having a brome mosaic virus protein coat and a functionalized gold core. The present study indicates that functionalized gold particles can initiate VLP assembly by mimicking the electrostatic behavior of the nucleic acid component of the native virus. These VLP constructs are symmetric, with the protein stoichiometry and packaging properties indicating similarity to the icosahedral packing of the capsid. Moreover, a pH-induced swelling transition of the VLPs is observed, in direct analogy to the native virus.     

Inhibition of HSV‐1 Attachment,Entry, and Cell‐to‐Cell Spread by Functionalized Multivalent Gold Nanoparticles

The use of modified nanoparticles in interactions with biological targets is attracting rapidly increasing attention. In this Full Paper, the application of gold nanoparticles capped with mercaptoethanesulfonate (Au‐MES NPs) as effective inhibitors of Herpes simplex virus type 1 infection based on their ability to mimic cell‐surface‐receptor heparan sulfate is described. Mechanistic studies reveal that Au‐MES NPs interfere with viral attachment, entry, and cell‐to‐cell spread, thereby preventing subsequent viral infection in a multimodal manner. The ligand multiplicity achieved with carrier nanoparticles is crucial in generating polyvalent interactions with the virus at high specificity, strength, and efficiency. Such multivalent‐nanoparticle‐mediated inhibition is a promising approach for alternative antiviral therapy.     

Kinetic study of gold nanoparticle growth in solution by Brust-Schiffrin reaction

Nanoparticle growth in solution is a rather complicated process governed by many thermodynamic and kinetics factors. A better understanding of nanoparticle growth kinetics is of primary importance leading to a better control on the nanoparticle size and size distribution. In this work we conducted both experimental and theoretical study on the kinetics of Brust-Schiffrin reaction for the synthesis of gold nanoparticles. Using an excessive amount of thiol ligands, the nanoparticle growth was stopped at different intermediate stages. Our study revealed and confirmed that the reproducibility of Brust-Schiffrin reaction for the synthesis of gold nanoparticles with diameters around 2 nm is rather poor due to the intrinsic complexity of this two-phase reaction. The analysis results of each intermediate product by TEM showed that nanoparticles grew very rapidly at the early stage of reaction and reached a maximum value of 2.6 nm at reaction time of around 10 minutes. Further increase of reaction time led to a decrease of nanoparticle size. In addition to the experimental study, we proposed a kinetic model for nanoparticle growth in solution by assuming that the nanoparticle core expands through incremental addition of gold atoms to the existing nanoparticle nuclei. This model not only gave a relatively good fitting to the experimental data, but also provided further insight into the nucleation and core expansion stage of the nanoparticle growth, which had not been revealed in previous modeling studies.     

Site‐Specific Modification of Adeno‐Associated Viruses via a Genetically Engineered Aldehyde Tag

As a consequence of their well‐defined nanostructure and intrinsic bioactive functionality, virus‐based nanoparticles have shown promise for mediating gene delivery. Adeno‐associated virus (AAV) nanoparticles, which possess an excellent safety profile and therapeutic potential, hold potential for use in human gene therapy. However, because of their native tropisms, the applicability of AAV nanoparticles is often limited to restricted ranges of cells or tissues. Thus, retargeting AAV particles to the desired cell populations has continued to be a major research focus in many gene therapy applications. In this study, a general strategy is reported for nanoparticle targeting. This involves the site‐specific modification of AAV type 2 (AAV2) by genetically incorporating a short peptide, in this case an aldehyde tag, in the viral capsid. Such a tag can be exploited for site‐specific attachment of targeting molecules and allows for further introduction of targeting antibodies or ligands. It is shown that this modification neither affects the level of infectious viral titer nor intracellular trafficking properties. Furthermore, the site‐specific conjugation of targeting antibodies could significantly enhance viral transduction to those target cells that have otherwise exhibited very low permissiveness to AAV2 infection. This method also allows the functional incorporation of RGD peptides onto AAV2 for enhanced delivery with implications for cancer gene therapy.     

The effect of cysteine on electrodeposition of gold nanoparticle

The most applications of gold nanoparticles are in the photo-electronical accessories and bio-chemical sensors. Chloride solution with cysteine additive was used as electrolyte in gold nanoparticles electrodeposition. The nucleation and growing mechanism were studied by electrochemical techniques such as cyclic voltammetry and chronoamperometry, in order to obtain a suitable nano structure. The deposition mechanism was determined as instantaneous nucleation and the dimension of particles was controlled in nanometric particle size range. Atomic Force Microscope was used to evaluate the effect of cysteine on the morphology and topography of gold nanoparticles. Finally the catalytic property of gold nanoparticle electrodeposited was studied in KOH solution, where oxygen reduction on the gold nanoparticle surface was eight times greater than that on the conventional gold deposits.     

Electronic properties of molecular memory circuits on a nanoscale scaffold

Significant challenges exist in assembling and interconnecting the building blocks of a nanoscale device and being able to electronically address or measure responses at the molecular level. Here we demonstrate the usefulness of engineered proteins as scaffolds for bottom-up self-assembly for building nanoscale devices out of multiple components. Using genetically engineered cowpea mosaic virus, modified to express cysteine residues on the capsid exterior, gold nanoparticles were attached to the viral scaffold in a specific predetermined pattern to produce specific interparticle distances. The nanoparticles were then interconnected using thiol-terminated conjugated organic molecules, resulting in a three-dimensional network. Network properties were engineered by using molecular components with different I-V characteristics. Networks consisting of molecular wires alone were compared with networks containing voltage controlled molecular switches with two stable conductance states. Using such bistable molecules enabled the formation of switchable molecular networks that could be used in nanoscale memory circuits.     

羟基化SBS模板合成金纳米粒子及表征

以羟基化SBS为模板,N,N-二甲基甲酰胺(DMF)为溶剂,氯金酸为原料,硼氢化钠为还原剂,在一定反应条件下制备得到了金纳米粒子。采用紫外-可见光谱和透射电子显微镜等方法对所合成的纳米金样品进行了表征。结果表明,羟基化SBS可以为金纳米粒子的成核和长大起到较好的模板作用,金纳米粒子可以产生纳米金所具有的表面等离子态的特征吸收峰;改变合成条件,可以控制金纳米粒子特征吸收峰的位置;透射电子显微镜给出金纳米粒子具有球状形貌特征,且具有较窄尺寸分布。     

Inhibition of influenza virus infection by multivalent sialic-acid-functionalized gold nanoparticles

An efficient synthesis of sialic-acid-terminated glycerol dendron to chemically functionalize 2 nm and 14 nm gold nanoparticles (AuNPs) is described. These nanoparticles are highly stable and show high activity towards the inhibition of influenza virus infection. As the binding of the viral fusion protein hemagglutinin to the host cell surface is mediated by sialic acid receptors, a multivalent interaction with sialic-acid-functionalized AuNPs is expected to competitively inhibit viral infection. Electron microscopy techniques and biochemical analysis show a high binding affinity of the 14 nm AuNPs to hemagglutinin on the virus surface and, less efficiently, to isolated hemagglutinin. The functionalized AuNPs are nontoxic to the cells under the conditions studied. This approach allows a new type of molecular-imaging activity-correlation and is of particular relevance for further application in alternative antiviral therapy.     

Optical properties of nanoparticle-based metallodielectric inverse opals

Metallodielectric inverse opals were prepared by co-crystallizing silica-coated gold nanoparticles and polymer spheres, followed by removal of the crystal template. The inverse opals exhibit a distinct reflectance peak, which results from Bragg diffraction due to the highly ordered 3D macroporous structure. Photonic band-structure calculations indicate that the characteristic reflectance peaks observed are signatures of the directional gap at the L point. It is demonstrated that the optical properties (the position and magnitude of the electromagnetic bandgaps) of the gold-silica nanocomposite inverse opals can be engineered by varying the nanoparticle morphology (core size and shell thickness) and/or the nanoparticle volume-filling ratio of the composite. The use of metallodielectric nanoparticles to form inverse opals offers a versatile approach to prepare photonic materials that may exhibit absolute bandgaps.     

Fabrication and optical characteristics of a novel optical fiber doped with the Au nanoparticles

Optical fibers containing gold metal nanoparticles were developed by modified chemical vapor deposition, in which Au(OH)3 and tetraethyl-orthosilicate (TEOS) was used via sol-gel process to incorporate gold metals by providing the reduction atmosphere. The absorption peak appeared near 490 nm was found to be due to the surface plasmon resonance of the gold nanoparticles incorporated in the fiber core.     

Synthesis of uniform and stable silver nanoparticles by a gold seed-mediated growth approach in a buffer system

A seeding growth approach to the preparation of silver nanoparticles with a controllable size was developed. It contained a two-step reaction: the first step was gold seed clusters quickly generated by a chemical reaction using sodium borohydride as a reducing reagent; the second one was controllable silver nanoparticles were grown at the mild condition by using the mixed reducing reagents (hydroxylamine hydrochloride and sodium hydroxide) to form a buffer system. The gold core was beneficial for the crystalline of silver cations to form the nanoparticles and the buffer system which was composed of hydroxylamine hydrochloride and sodium hydroxide, and was helpful for controlling the size and shape of the as-prepared silver nanoparticles. These as-prepared nanoparticles were characterised by X-ray powder diffraction, UV-Vis spectroscopy (UV-Vis) and transmission electron microscopy along with energy dispersive X-ray spectroscopy. The results indicated that the obtained silver nanoparticles are highly crystallised with an average diameter around 10?nm. The content of gold seeds and the mild reaction rate controlled by the buffer system were considered to be key factors in the control of silver nanoparticles’ morphology and size. A possible mechanism of the silver nanoparticles formed was also proposed.     

Fluorescence labeling of human rhinovirus capsid and analysis by capillary electrophoresis

The capsid of human rhinovirus serotype 2, consisting of four viral proteins, was fluorescence-labeled with fluorescein isothiocyanate and analyzed by capillary electrophoresis using UV and laser-induced fluorescence detection. Heat denaturation, proteolytic digestion, and receptor binding were applied for confirmation of the identity of the peak with the labeled virus. Incomplete derivatization with the fluorophore preserved the affinity of the virus for its receptor, indicating that its cell entry pathway is unperturbed by this chemical modification; indeed, an infectivity assay confirms that the labeled virus samples are infectious. The results show that fluorescence labeling of the viral capsid might lead to a valuable probe for studying infection processes in the living cell.     

高分子基磁性纳米复合物的研究进展

磁性纳米颗粒由于具有不同于大块样品的物理和化学性质,因而在日常生活中具有广泛的应用并且日趋复杂.因此控制磁性纳米材料的稳定性及表面的功能化就变得尤为重要.聚合物作为覆盖层可以很好地控制磁性纳米颗粒的成核、生长和团聚,此外,两者复合后还可改善聚合物的性质.评述了近些年来聚合物磁性纳米复合物的研究进展,并提出了纳米复合物需要解决的问题.     

Ascorbic acid-mediated synthesis and characterisation of iron oxide/gold core–shell nanoparticles.

The current article reports on providing surface modification of magnetic nanoparticles with gold to provide stability against aggregation. Gold-coated magnetite nanoparticles were synthesised to combine both magnetic as well as surface plasma resonance (SPR) properties in a single moiety. The nanocomposites were produced by reduction (using ascorbic acid) of gold chloride on to the surface of iron oxide nanoparticles. Ascorbic acid not only acts as a reducing agent, but also the oxidised form of ascorbic acid i.e. Dehydro-ascorbic acid acts as a capping agent to impart stability to as synthesised gold-coated iron oxide nanocomposites. The synthesised nanocomposite was monodispersed with a mean particle size of around 16 nm and polydispersity index of 0.190. X-ray diffraction analysis confirms presence of gold on the surface of magnetite nanoparticles. The synthesised nanocomposites had a total organic content of around 3.2% w/w and also showed a shifted SPR peak at 546 nm as compared to gold nanoparticles (528 nm). Both uncoated and gold-coated magnetite exhibited superparamagnetic behaviour at room temperature. Upon coating with gold shell, saturation magnetisation of iron oxide nanoparticles decreases from 42.806 to 3.54 emu/gram.     

A facile synthesis of lipid stabilized gold nanoparticles: a step towards biodegradable biosensors

A new class of polylactone was successfully synthesized and utilized for the encapsulation and stabilization of gold nanoparticles. Core/shell nanoparticle architecture, in which a layer of this polymer surrounds the nanoparticle core have been investigated both as a means to improve the stability and surface chemistry and as a way of accessing unique physical properties that are not possible from one nano-material alone. Given the fact that only few systems has so far been developed for the encapsulation of nanoparticles, our success in using a new biodegradable biopolymer with inbuilt functionality reveals the robustness of this work. The biodegradability of this polylactone was evaluated using scanning electron microscopy (SEM). The morphology and stability of these gold-polymer hybrids were evaluated by using the transmission electron microscopy (TEM) and UV-VIS spectroscopy.     

Spectroscopic characterization of gold nanoparticles formed by cells and S-layer protein of Bacillus sphaericus JG-A12

The strain Bacillus sphaericus JG-A12, isolated from a uranium mining waste pile near the town of Johanngeorgenstadt, is capable of selective and reversible accumulation of U, Cu, Pb, Al, and Cd from uranium waste waters. The cells of this strain are enveloped by a surface layer protein (S-layer). The highly regular structure of this S-layer with many pores of identical size offers good binding sites for different kinds of molecules and provides nucleation sites for the formation of metal nanoclusters or minerals. In this study we demonstrate that B. sphaericus JG-A12 cells and their purified S-layer protein were capable to reduce Au to metallic nanoclusters in the presence of reducing agents such as molecular H₂. The gold nanoparticles were regularly distributed and sized according to the pores of the protein lattice. The metallic nature of the clusters was confirmed by different techniques such as extended X-ray absorption fine structure (EXAFS) spectroscopy, X-ray absorption near edge (XANES) spectroscopy, UV–vis spectroscopy and X-ray powder diffraction (XRD). The size of the gold nanoparticles was estimated to be almost 1 nm. Our results demonstrate that B. sphaericus JG-A12 can be used to prepare gold nanoparticles tailor-made for industrial applications.