Andrew M. Shaw

Silver nanoparticle enhanced silver ion stress response in Escherichia coli K12

Abstract This study investigated the dissolution-based toxicity mechanism for silver nanoparticles to Escherichia coli K12. The silver nanoparticles, synthesised in the vapour phase, are effective anti-bacterial agents against the Gram-negative bacterium, E. coli K12. The nanoparticles associate with the bacterial cell wall, appearing to interact with the outer and inner membranes, and then dissolve to release Ag+ into the cell and affect a transcriptional response. The dissolution of these nanoparticles in a modified LB medium was measured by inductively coupled plasma mass spectrometry (ICP-MS) and has been shown to follow a simple first-order dissolution process proportional to the decreasing surface area of the nanoparticles. However, the resulting solution phase concentration of Ag+, demonstrated by the ICP-MS data, is not sufficient to cause the observed effects, including inhibition of bacterial growth and the differential expression of Cu+ stress response genes. These data indicate that dissolution at the cell membrane is the primary mechanism of action of silver nanoparticles, and the Ag+ concentration released into the bulk solution phase has only limited anti-bacterial efficacy.

Microwave spectroscopy and interaction potential of the long‐range He...Ar+ ion

We have measured and interpreted a microwave spectrum of the HeAr+ ion in which all of the observed energy levels lie within 8 cm−1 of the lowest dissociation limit, He(1S)+Ar+(2P3/2). We use an ion beam technique in which the HeAr+ ions are formed by electron impact, accelerated to kilovolt potentials, and mass‐analyzed. After passage through an appropriate section of waveguide, the ions enter an electric field lens in which state‐selective fragmentation occurs; the Ar+ ions produced in the lens are separated from all other ions by means of an electrostatic analyser and detected with an electron multiplier. Microwave transitions induced in the waveguide section result in population transfer which produces detected changes in the electric field‐induced Ar+ fragment current. Many transitions have also been observed by a microwave–microwave double resonance technique. We have observed 68 lines spanning the frequency range 6–170 GHz; no immediately recognizable pattern is apparent. We have measured the Zeema...

A gold nanoparticle-linked glycoconjugate vaccine against Burkholderia mallei

UNLABELLED Burkholderia mallei are Gram-negative bacteria, responsible for the disease glanders. B. mallei has recently been classified as a Tier 1 agent owing to the fact that this bacterial species can be weaponised for aerosol release, has a high mortality rate and demonstrates multi-drug resistance. Furthermore, there is no licensed vaccine available against this pathogen. Lipopolysaccharide (LPS) has previously been identified as playing an important role in generating host protection against Burkholderia infection. In this study, we present gold nanoparticles (AuNPs) functionalised with a glycoconjugate vaccine against glanders. AuNPs were covalently coupled with one of three different protein carriers (TetHc, Hcp1 and FliC) followed by conjugation to LPS purified from a non-virulent clonal relative, B. thailandensis. Glycoconjugated LPS generated significantly higher antibody titres compared with LPS alone. Further, they improved protection against a lethal inhalation challenge of B. mallei in the murine model of infection. FROM THE CLINICAL EDITOR Burkholderia mallei is associated with multi-drug resistance, high mortality and potentials for weaponization through aerosol inhalation. The authors of this study present gold nanoparticles (AuNPs) functionalized with a glycoconjugate vaccine against this Gram negative bacterium demonstrating promising results in a murine model even with the aerosolized form of B. Mallei.

Differential gene regulation in the Ag nanoparticle and Ag+-induced silver stress response in Escherichia coli: A full transcriptomic profile

Abstract We report the whole-transcriptome response of Escherichia coli bacteria to acute treatment with silver nanoparticles (AgNPs) or silver ions [Ag(I)] as silver nitrate using gene expression microarrays. In total, 188 genes were regulated by both silver treatments, 161 were up-regulated and 27 were down-regulated. Significant regulation was observed for heat shock response genes in line with protein denaturation associated with protein structure vulnerability indicating Ag(I)-labile –SH bonds. Disruption to iron–sulphur clusters led to the positive regulation of iron–sulphur assembly systems and the expression of genes for iron and sulphate homeostasis. Further, Ag ions induced a redox stress response associated with large (>600-fold) up-regulation of the E. coli soxS transcriptional regulator gene. Ag(I) is isoelectronic with Cu(I), and genes associated with copper homeostasis were positively regulated indicating Ag(I)-activation of copper signalling. Differential gene expression was observed for the silver nitrate and AgNP silver delivery. Nanoparticle delivery of Ag(I) induced the differential regulation of 379 genes; 309 genes were uniquely regulated by silver nanoparticles and 70 genes were uniquely regulated by silver nitrate. The differential silver nanoparticle–silver nitrate response indicates that the toxic effect of labile Ag(I) in the system depends upon the mechanism of delivery to the target cell.

Crystal structure of a soluble form of human CD73 with ecto-5'-nucleotidase activity.

CD73 is a dimeric ecto‐5′‐nucleotidase that is expressed on the exterior side of the plasma membrane. CD73 has important regulatory functions in the extracellular metabolism of certain nucleoside monophosphates, in particular adenosine monophosphate, and has been linked to a number of pathological conditions such as cancer and myocardial ischaemia. Here, we present the crystal structure of a soluble form of human soluble CD73 (sCD73) at 2.2 Å resolution, a truncated form of CD73 that retains ecto‐5′‐nucleotidase activity. With this structure we obtained insight into the dimerisation of CD73, active site architecture, and a sense of secondary modifications of the protein. The crystal structure reveals a conserved loop that is directly involved in the dimer‐dimer interaction showing that the two subunits of the dimer are not linked by disulfide bridges. Using biophotonic microarray imaging we were able to confirm glycosylation of the enzyme and show that the enzyme is decorated with a variety of oligosaccharide structures. The crystal structure of sCD73 will aid the design of inhibitors or activator molecules for the treatment of several diseases and prove useful in explaining the possible roles of single nucleotide polymorphisms in physiology and disease.

Whole serum BSA antibody screening using a label-free biophotonic nanoparticle array

Bovine serum albumin antibodies (aBSA) have been screened from whole leporine anti serum on a biophotonic array. The array was initially printed with seed gold nanoparticles into a 96-spot configuration, and 130-nm gold nanoparticles were synthesised in situ on the surface of each spot. The gold nanoparticle surface was then functionalized with the proteins bovine serum albumin (BSA), fibrinogen, and immunoglobulin G (IgG) and with the amino acid glycine. The concentration of aBSA in the whole serum was determined using a kinetic analysis of the time-dependent light scattering from the nanoparticles. The aBSA-BSA kinetic parameters derived from the array are k(a)=(1.3 +/- 0.3) x 10(5) M(-1) s(-1), k(d)=(4 +/- 2) x 10(-4) s(-1), and K(D)=3 nM, which compare favorably with those from continuous gold surfaces. The ultimate sensitivity of the array reader to the bulk refractive index (RI) is 1 x 10(-4) refractive index units (RIU), corresponding to 1 microg ml(-1) for aBSA. The nanoparticles appear to be more sensitive than the continuous gold surface to the aBSA binding event from whole serum, and this is interpreted in terms of the difference in RI contrast in the plasmon fields.

Synthesis of the germination stimulant (±)-strigol

Two synthetic routes to the octahydroindeno[1,2-b]furanone derivative strigol (1), a germination stimulant of witchweed seeds, and its stereoisomers are described.

Microwave electronic spectrum of the Ne⋯Ne+ long-range complex: The interaction potential

The full interaction potential between Ne(1S) and Ne+(2P) is determined by least-squares fitting of potential parameters to spectroscopic data, principally from the near-dissociation microwave spectra of the Ne2+ complex. The potential obtained in this way incorporates the potential curves for all six electronic states correlating with Ne(1S)+Ne+(2P) and the couplings between them. Coupled-channel calculations on the potential take account of breakdown of the Born–Oppenheimer approximation and provide an accurate description of the microwave rovibronic spectrum involving levels within ∼10 cm−1 of the first dissociation limit. The Ne2+ ions are both vibrationally and rotationally hot: the spectrum involves levels up to at least J=25/2 and there is evidence for transitions involving levels near the second dissociation limit. The long-range levels involved have 〈r〉 up to 12 A, compared with an equilibrium bond length of 1.756 A for the ground electronic state. The long-range parameters of the interaction can...

Microwave spectroscopy and interaction potential of the long‐range He⋯Kr+ ion: An example of Hund’s case (e)

We have observed a microwave spectrum of the HeKr+ ion in which all of the observed levels lie within a few cm−1 of either the first or second dissociation limit. We use an ion beam technique in which HeKr+ ions, formed by electron impact, are mass analyzed. Passage of the ion beam through an electric field lens results in selective fragmentation of energy levels lying close to dissociation. Kr+ ions formed in the lens are separated from all other ions by means of an electrostatic analyzer, and are detected with an electron multiplier. Microwave radiation induces transitions which result in population transfer and produce detected changes in the electric field‐induced Kr+ fragment ion current. Additional transitions have been detected by a microwave–microwave double resonance method, and we have also made extensive use of the Zeeman effects produced by small applied coaxial magnetic fields to identify the J quantum numbers of the levels involved. Coupled channel calculations of the bound states of the He⋯...

Label-free antibody-antigen binding detection by optical sensor array based on surface-synthesized gold nanoparticles.

Gold nanoparticles grown in situ from printed seed particles on a glass substrate have been fabricated into a biosensor array. The light-scattering properties of the resulting surfaces show sensitivity to changes in the local refractive index. Each array spot is functionalized with fibrinogen or bovine serum albumin and scattered radiation is used to monitor the refractive index change on label-free binding of the antibodies to their antigens from whole blood antiserum. Data were collected real-time and the association rate constants for the specific antibody-antigen binding were derived from a kinetic analysis. The minimum antibody concentration detection sensitivity is of 100 nM.