Multiplexed paper test strip for quantitative bacterial detection

Rapid, sensitive, on-site detection of bacteria without a need for sophisticated equipment or skilled personnel is extremely important in clinical settings and rapid response scenarios, as well as in resource-limited settings. Here, we report a novel approach for selective and ultra-sensitive multiplexed detection of Escherichia coli (non-pathogenic or pathogenic) using a lab-on-paper test strip (bioactive paper) based on intracellular enzyme (β-galactosidase (B-GAL) or β-glucuronidase (GUS)) activity. The test strip is composed of a paper support (0.5 × 8 cm), onto which either 5-bromo-4-chloro-3-indolyl-β-D: -glucuronide sodium salt (XG), chlorophenol red β-galactopyranoside (CPRG) or both and FeCl(3) were entrapped using sol-gel-derived silica inks in different zones via an ink-jet printing technique. The sample was lysed and assayed via lateral flow through the FeCl(3) zone to the substrate area to initiate rapid enzyme hydrolysis of the substrate, causing a change from colorless-to-blue (XG hydrolyzed by GUS, indication of nonpathogenic E. coli) and/or yellow to red-magenta (CPRG hydrolyzed by B-GAL, indication of total coliforms). Using immunomagnetic nanoparticles for selective preconcentration, the limit of detection was ~5 colony-forming units (cfu) per milliliter for E. coli O157:H7 and ~20 cfu/mL for E. coli BL21, within 30 min without cell culturing. Thus, these paper test strips could be suitable for detection of viable total coliforms and pathogens in bathing water samples. Moreover, inclusion of a culturing step allows detection of less than 1 cfu in 100 mL within 8 h, making the paper tests strips relevant for detection of multiple pathogens and total coliform bacteria in beverage and food samples.     

Almost Cross-Intersecting and Almost Cross-Sperner Pairs of Families of Sets

For a set G and a family of sets ${\mathcal{F}}$ let ${\mathcal{D}_{\mathcal{F}}(G)=\{F\in \mathcal{F}:F\cap G=\emptyset\}}$ and ${\mathcal{S}_{\mathcal{F}}(G)=\{F\in\mathcal{F}:F\subseteq G\,{\rm or} \,G \subseteq F\}.}$ We say that a family is l-almost intersecting, (≤ l)-almost intersecting, l-almost Sperner, (≤ l)-almost Sperner if ${|\mathcal{D}_{\mathcal{F}}(F)|=l, |\mathcal{D}_{\mathcal{F}}(F)|\le l, |\mathcal{S}_{\mathcal{F}}(F)|=l, |\mathcal{S}_{\mathcal{F}}(F)| \le l}$ (respectively) for all ${F \in \mathcal{F}.}$ We consider the problem of finding the largest possible family for each of the above properties. We also address the analogous generalization of cross-intersecting and cross-Sperner families.     

The Imidazopyridine Derivative JK184 Reveals Dual Roles for Microtubules in Hedgehog Signaling

Eradicating hedgehogs : The title molecule has been previously identified as a potent inhibitor of the Hedgehog signaling pathway, which gives embryonic cells information needed to develop properly. This molecule is shown to modulate Hedgehog target gene expression by depolymerizing microtubules, thus revealing dual roles of the cytoskeleton in pathway regulation (see figure).

     

Pulse error compensating symmetric magic-echo trains

We present improved line-narrowing sequences for dipolar coupled spin systems, based on a train of magic-echoes which are compensated for the effects of finite pulse widths and utilize symmetry properties of supercycles. Sequences are introduced for spectroscopy and imaging by proper choice of a phase alternating scheme. Using a 16 pulse time-suspension magic-echo cycle, the highest level of line-narrowing achieved was 2.7 Hz for the [100] direction of a single crystal of calcium fluoride, a reduction in linewidth by 4 orders of magnitude.     

Implementation of the quantum Fourier transform

A quantum Fourier transform (QFT) has been implemented on a three qubit nuclear magnetic resonance (NMR) quantum computer to extract the periodicity of an input state. Implementation of a QFT provides a first step towards the realization of Shor's factoring and other quantum algorithms. The experimental implementation of the QFT on a periodic state is presented along with a quantitative measure of its efficiency measured through state tomography. Experimentally realizing the QFT is a clear demonstration of the ability of NMR to control quantum systems.     

Multiple pulse NMR imaging of polymers and chemistry.

Multiple pulse line narrowing techniques can be used to improve resolution and sensitivity in solid state NMR imaging. For example, pulse sequences which remove homonuclear dipolar broadening have been used to image proton-containing materials. Further enhancements in resolution and sensitivity are obtained by removing inhomogeneous interactions such as chemical shift, susceptibility, and heteronuclear dipolar broadening. Pulse sequences have been designed which provide efficient line narrowing over large spectral widths by taking into account the experimenter's control over the amplitude and time dependence of the gradient-induced resonance offset. These methods have been applied to centimeter sized samples to obtain images of polymers, composite materials, and gas-solid chemical reactions. T1 and T2 contrast allows differentiation between materials.     

Quantum process tomography of the quantum Fourier transform

The results of quantum process tomography on a three-qubit nuclear magnetic resonance quantum information processor are presented and shown to be consistent with a detailed model of the system-plus-apparatus used for the experiments. The quantum operation studied was the quantum Fourier transform, which is important in several quantum algorithms and poses a rigorous test for the precision of our recently developed strongly modulating control fields. The results were analyzed in an attempt to decompose the implementation errors into coherent (overall systematic), incoherent (microscopically deterministic), and decoherent (microscopically random) components. This analysis yielded a superoperator consisting of a unitary part that was strongly correlated with the theoretically expected unitary superoperator of the quantum Fourier transform, an overall attenuation consistent with decoherence, and a residual portion that was not completely positive-although complete positivity is required for any quantum operation. By comparison with the results of computer simulations, the lack of complete positivity was shown to be largely a consequence of the incoherent errors which occurred over the full quantum process tomography procedure. These simulations further showed that coherent, incoherent, and decoherent errors can often be identified by their distinctive effects on the spectrum of the overall superoperator. The gate fidelity of the experimentally determined superoperator was 0.64, while the correlation coefficient between experimentally determined superoperator and the simulated superoperator was 0.79; most of the discrepancies with the simulations could be explained by the cumulative effect of small errors in the single qubit gates.     

Entanglement assisted metrology

We propose a new approach to the measurement of a single spin state, based on nuclear magnetic resonance (NMR) techniques and inspired by the coherent control over many-body systems envisaged by quantum information processing. A single target spin is coupled via the magnetic dipolar interaction to a large ensemble of spins. Applying radio frequency pulses, we can control the evolution so that the spin ensemble reaches one of two orthogonal states whose collective properties differ depending on the state of the target spin and are easily measured. We first describe this measurement process using quantum gates; then we show how equivalent schemes can be defined in terms of the Hamiltonian and thus implemented under conditions of real control, using well established NMR techniques. We demonstrate this method with a proof of principle experiment in ensemble liquid state NMR and simulations for small spin systems.     

Chemistry of phosphine-borane adducts at platinum centers: dehydrocoupling reactivity of Pt(II) dihydrides with P-H bonds

The reaction of the Pt(II) dihydride complex cis-[PtH2(dcype)](dcype = 1,2-bis(dicyclohexylphosphino)ethane) with the primary or secondary phosphine-borane adducts PhRPH x BH3(R = H, Ph) was found to exclusively afford the mono-substituted complexes cis-[PtH(PPhR x BH3)(dcype)](1: R = H; 2: R = Ph)via a dehydrocoupling reaction between Pt-H and P-H bonds. Similar reactivity was observed between the uncoordinated phosphines PhRPH (R = H, Ph) and cis-[PtH2(dcype)], which gave cis-[PtH(PPhR)(dcype)](4: R = H; 5: R = Ph). The complexes were characterized by 1H, 11B, 13C and 31P NMR spectroscopy, IR, MS and, in the case of 2, X-ray crystallography that confirmed the cis geometries. The di-substituted complex cis-[Pt(PhPH x BH3)2(dcype)](3) was prepared from the reaction of cis-[PtCl2(dcype)] with two equivalents of Li[PPhH x BH3]. This suggested that steric reasons alone cannot be used to explain the lack of reactivity with respect to a second dehydrocoupling reaction involving the remaining Pt-H bond in complexes 1, 2, 4 and 5.