Measurement of the binding of cholera toxin to GM1 gangliosides on solid supported lipid bilayer vesicles and inhibition by europium (III) chloride

In this paper the immobilization of small unilamellar DMPC/GM1 lipid vesicles containing a water-soluble bodipy dye is described. The binding of the complete alphabeta toxin expressed by Vibrio cholerae to the attached vesicles was measured using Surface Plasmon Resonance (SPR) and a value of the dissociation constant K d obtained. Further measurements showed that the interaction of both the alphabeta-toxin and the beta-subunit alone resulted in the permeation of the lipid membrane, with release of a fluorophore contained within the vesicle being measured by combined SPR and Surface Plasmon enhanced Fluorescence Spectroscopy (SPFS). The leakage of dye through the membrane, measured by following the change in fluorescence, was fitted to a simple diffusion model. Finally, SPFS measurements of the effect of europium(III) chloride (EuCl 3) showed that cholera toxin binding and subsequent membrane permeation could be blocked by 1 micromol dm (-3) europium chloride. In view of the low oral toxicity of europium chloride, we speculate on the potential pharmaceutical applications of this molecule in the treatment of cholera infection.     

Bioinspired core‐crosslinked micelles from thymine‐functionalized amphiphilic block copolymers: Hydrogen bonding and photo‐crosslinking study

Bioinspired core‐bound polymeric micelles, based on hydrogen bonding and photo‐crosslinking, of thymine have been prepared from poly(vinylbenzylthymine)‐b‐poly(vinylbenzyltriethylammonium chloride). The amphiphilic block copolymer was synthesized by 2,2‐tetramethylpiperidin‐1‐oxyl‐mediated living radical polymerization in water/ethylene glycol solution. Micelle characterization and critical micelle concentration measurements demonstrated that the hydrogen bonding of the attached thymine units stabilizes the micelles. Further, core‐crosslinked polymeric micelles were formed by ultraviolet (UV) radiation showing that the stability of the micelle could be controlled by the UV crosslinking of the attached thymines. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011     

The Interaction of Serum Albumin with Cholesterol Containing Lipid Vesicles

In this paper, the interaction of both human blood serum (the primary fraction of which is serum albumin) and pure human serum albumin (HSA) with surface immobilised lipid vesicles was measured by combined Surface Plasmon Resonance (SPR) and Surface Plasmon enhanced Fluorescence (SPEFS), and fluorescence microscopy. It was found that both blood serum and HSA showed specific binding to vesicles which contained cholesterol, resulting in increased membrane permeability and release of encapsulated fluorescent dye. This effect was not seen with heat inactivated blood serum, heat inactivated HSA or in vesicles not containing cholesterol. These results suggest that HSA may have a physiological role over and beyond that of fatty acid carrier, possibly acting to regulate vascular endothelial cell cholesterol concentration.     

STATUS DIFFERENTIATION AND THE COHESION OF SOCIAL NETWORKS

This article examines the effects of status differentiation on the cohesion of a social structure. Using a formal model, we simulate the fates of a hypothetical cohort of newly hired employees, who are equals in the eyes of their boss and in the nascent stages of sorting into a status hierarchy. We cast these employees in a process in which they exert effort, receive public approval from the boss in exchange, and thus come to fill different places in a status order. We then consider the circumstances under which these workers cohere as a group and when, by contrast, differentiation makes cohesion among them unlikely. Our results show that the extent of the boss's autonomy in relationship to employees accounts for this difference in outcomes. Under an autonomous boss, as differentiation transpires, status-based social forces break the group of workers apart. Conversely, when the boss occupies a compromised position, group-level cohesion coexists with differentiation. Our main contribution is the intuition that the cohesion-related consequences of status differentiation can substantially depend on the tie between contestants and their external audience. We conclude by developing conjectures for empirical research consistent with our main findings.     

Suzuki-Miyaura cross-coupling of 3-pyridyl triflates with 1-alkenyl-2-pinacol boronates

Palladium-catalyzed Suzuki-type couplings of 3-pyridyl triflates with alkenyl pinacol boronates proceed in good to excellent yield. Optimized conditions use Pd(PPh(3))(4) (10 mol %) as catalyst with K(3)PO(4) (3 equiv) as base in dioxane.     

An electrochemical impedance study of the effect of pathogenic bacterial toxins on tethered bilayer lipid membrane

Pathogenic bacteria secrete various virulence factors that can directly interact with the outer lipid bilayer membrane of eukaryotic cells, inducing cell death by apoptosis or necrosis. Such virulence factors account for much of the toxic action associated with bacterial infection; therefore the detection of such proteins could provide a methodology for sensing/detection of pathogenic bacteria in, for example, food or human tissue. Detection and identification of pathogenic bacteria by conventional methods such as plating and counting in laboratory is expensive and time consuming. With growing concerns over emergence and re-emergence of pathogenic bacteria with high resistant to current antibiotics, there is a potential need for effective detection of pathogenic toxins in-vitro. This paper presents the application of tethered bilayer lipid membrane (TBLM) as a sensing platform for the detection of the clinically relevant pathogenic bacterial, Staphylococcus aureus MSSA 476 and Pseudomonas aeruginosa PAO1 via their secreted virulence factors, using electrochemical impedance spectroscopy (EIS). A non-pathogenic strain of bacteria, E. coli DH5α was used as a control. A clear difference in the impedance of the TBLM for the pathogenic vs. non-pathogenic species was observed.     

Targeted data acquisition for improved reproducibility and robustness of proteomic mass spectrometry assays

Quantitative mass spectrometry-based proteomic assays often suffer from a lack of robustness and reproducibility. We here describe a targeted mass spectrometric data acquisition strategy for affinity enriched subproteomes—in our case the kinome—that enables a substantially improved reproducibility of detection, and improved quantification via isobaric tags. Inclusion mass lists containing m/z, charge state, and retention time were created based on a set of 80 shotgun-type experiments performed under identical experimental conditions. For each target protein, peptides were selected according to their frequency of observation and isobaric tag for relative and absolute quantitation (iTRAQ) reporter ion quality. Retention times of selected peptides were aligned using similarity driven pairwise alignment strategy yielding <1 min standard deviation for 4 h gradients. Multiple fragmentation of the same peptides resulted in better statistics and more precise reporter ion based quantification without any loss in coverage. Overall, 24% more target proteins were quantified using the targeted data acquisition approach, and precision of quantification improved by >1.5-fold. We also show that a combination of higher energy collisional dissociation (HCD) with collisional induced dissociation (CID) outperformed pulsed-Q-dissociation (PQD) on the OrbitrapXL. With the CID/ HCD based targeted data acquisition approach 10% more quantifiable target proteins were identified and a 2-fold increase in quantification precision was achieved. We have observed excellent reproducibility between different instruments, underlining the robustness of the approach.     

Offline estimation of decay time for an optical cavity with a low pass filter cavity model

This Letter presents offline estimation results for the decay-time constant for an experimental Fabry-Perot optical cavity for cavity ring-down spectroscopy (CRDS). The cavity dynamics are modeled in terms of a low pass filter (LPF) with unity DC gain. This model is used by an extended Kalman filter (EKF) along with the recorded light intensity at the output of the cavity in order to estimate the decay-time constant. The estimation results using the LPF cavity model are compared to those obtained using the quadrature model for the cavity presented in previous work by Kallapur et?al. The estimation process derived using the LPF model comprises two states as opposed to three states in the quadrature model. When considering the EKF, this means propagating two states and a (2×2) covariance matrix using the LPF model, as opposed to propagating three states and a (3×3) covariance matrix using the quadrature model. This gives the former model a computational advantage over the latter and leads to faster execution times for the corresponding EKF. It is shown in this Letter that the LPF model for the cavity with two filter states is computationally more efficient, converges faster, and is hence a more suitable method than the three-state quadrature model presented in previous work for real-time estimation of the decay-time constant for the cavity.     

Inhomogeneity of electron injection rates in dye-sensitized TiO2: comparison of the mesoporous film and single nanoparticle behavior

As it has been shown by pump-probe experiments electron injection at the interface between a dye molecule and mesoporous TiO2 proceeds with rates exceeding 1 x 10(13) s(-1). However, similar dye-TiO2 systems exhibit residual dye emission with lifetimes extending into the long nanosecond range. To address this inhomogeneity of injection rates time-correlated single photon counting microscopy was used to compare the emission behavior of dye-sensitized mesoporous films of TiO2 with that of individual anatase nanoparticles that had undergone extensive dialysis. The sensitized films produce intense residual emission with multiexponential decay components as long as 220 ns. The channels of mesoporous films contain physisorbed and trapped dye, which is the dominant source of the emission. It is likely that the wide range of lifetimes reflects the distribution of mean free paths experienced by the loose dye molecules diffusing within the film prior to undergoing oxidative quenching. In contrast, the intensity of emission from individual nanoparticles from which the loose dye was removed by dialysis is orders of magnitude lower. The lifetimes obtained from such particles are much shorter, with the primary component on a sub-nanosecond time scale. The presence of residual emission with a 230 ps lifetime shows that even on the surfaces of dialyzed nanoparticles there is a fraction of sensitizer molecules that do not inject electrons with the same high rate as is observed in ultrafast pump-probe experiments on films. Since the physisorbed dye was removed from these samples by dialysis, the residual emission is likely to originate from dye molecules bound to surface defects. Unusual collective emission bursts were observed in some of the measurements on sensitized nanoparticles. We attribute this behavior to stimulated emission from individual nanocrystallites.