Light-Independent Inactivation of Dengue-2 Virus by Carboxyfullerene C3 Isomer

AbstractCarboxyfullerene (C60) is known as a photosensitizer for virus inactivation. Its regioisomer with C3 symmetry, named the C3 isomer, could also inactivate the dengue-2 virus without light when the dose of C3 isomer was increased to 40 μM, indicating the possible involvement of a light-independent mechanism. Further analysis showed that the C3 isomer blocked viral replication at the attachment and penetration stages, suggesting that a direct interaction between the C3 isomer and the virion is required for inactivation. The C3 isomer with a bipolar structure showed better lipid interaction and dengue-2 virus suppression than D3, another isomer that contains evenly distributed hydrophilic side chains. Moreover, the C3 isomer selectively inactivated enveloped viruses (viz., dengue-2 virus and Japanese encephalitis virus) instead of nonenveloped viruses (viz., enterovirus 71 and coxsackievirus B3). Collectively, these findings support the hypothesis that C3 isomer suppression of enveloped viruses is effected through its hydrophobic interaction with the viral lipid envelope. Our report, which demonstrates the light-dependent and -independent mechanisms of C60 on viral inactivation, will aid in the development of novel anti-viral agents for use against enveloped viruses

Resolving the polarization puzzles in D0→VVD^0\to VV

We carry out a systematic analysis of the Cabbibo-favored (CF) and singly Cabbibo-suppressed (SCS) decays of $D^0\to VV$, and demonstrate that the long-distance mechanism due to the final-state interactions (FSIs) can provide a natural explanation for these mysterious polarization puzzles observed in $D^0\to VV$ in experiment. More observables, which can be measured at BESIII and possibly at LHCb, are also suggested.Comment: Revtex, 2 figures, 14 pages; extended version with the detailed formalisms include

Evolution of anthropogenic air pollutant emissions in Guangdong Province, China, from 2006 to 2015

Guangdong Province (GD), one of the most prosperous and populous regions in China, still experiences haze events and growing ozone pollution in spite of the substantial air-quality improvement in recent years. Integrated control of fine particulate matter (PM2.5) and ozone in GD calls for a systematic review of historical emissions. In this study, emission trends, spatial variations, source-contribution variations, and reduction potentials of sulfur dioxide (SO2), nitrogen oxides (NO), PM2.5, inhalable particles (PM10), carbon monoxide (CO), ammonia (NH3), and volatile organic compounds (VOCs) in GD from 2006 to 2015 were first examined using a dynamic methodology, taking into account economic development, technology penetration, and emission controls. The relative change rates of anthropogenic emissions in GD during 2006-2015 are -48% for SO2, -0.5% for NO, -16% for PM2.5, -22% for PM10, 13% for CO, 3% for NH3, and 13% for VOCs. The declines of SO2, NO, PM2.5, and PM10 emissions in the whole province mainly resulted from the stringent emission control in the Pearl River delta (PRD) region, where most previous control measures were focused, especially on power plants (SO2 and NO), industrial combustion (SO2, PM2.5, PM10), on-road mobile sources (NO), and dust sources (PM2.5 and PM10). Emissions from other areas (non-PRD, NPRD), nevertheless, remain relatively stable due to the lax control measures and rapidly growing energy consumption. In addition, emission leaks of SO2 and NO from industries are observed from PRD to NPRD in 2010 and 2011. As a result, emissions in NPRD are increasingly important in GD, particularly those from industrial combustion. The contribution of NPRD to the total SO2 emissions in GD, for example, increased from 27% in 2006 to 48% in 2015. On-road mobile sources and solvent use are the two key sources that should receive more effective control measures in GD. Current control-driven emission reductions from on-road mobile sources are neutralized by the substantial growth of the vehicle population, while VOC emissions in GD steadily increase due to the growth of solvent use and the absence of effective control measures. Besides, future work could focus on power plants and industrial combustion in GD and industrial process sources in NPRD, which still have large emission reduction potentials. The historical emission inventory developed in this study not only helps to understand the emission evolution in GD, but also provides robust data to quantify the impact of emission and meteorology variations on air quality and unveil the primary cause of significant air-quality change in GD in the recent decade

Janus monolayers of transition metal dichalcogenides.

Structural symmetry-breaking plays a crucial role in determining the electronic band structures of two-dimensional materials. Tremendous efforts have been devoted to breaking the in-plane symmetry of graphene with electric fields on AB-stacked bilayers or stacked van der Waals heterostructures. In contrast, transition metal dichalcogenide monolayers are semiconductors with intrinsic in-plane asymmetry, leading to direct electronic bandgaps, distinctive optical properties and great potential in optoelectronics. Apart from their in-plane inversion asymmetry, an additional degree of freedom allowing spin manipulation can be induced by breaking the out-of-plane mirror symmetry with external electric fields or, as theoretically proposed, with an asymmetric out-of-plane structural configuration. Here, we report a synthetic strategy to grow Janus monolayers of transition metal dichalcogenides breaking the out-of-plane structural symmetry. In particular, based on a MoS2 monolayer, we fully replace the top-layer S with Se atoms. We confirm the Janus structure of MoSSe directly by means of scanning transmission electron microscopy and energy-dependent X-ray photoelectron spectroscopy, and prove the existence of vertical dipoles by second harmonic generation and piezoresponse force microscopy measurements

Microarray-based estimation of SNP allele-frequency in pooled DNA using the Langmuir kinetic model

<p>Abstract</p> <p>Background</p> <p>High throughput genotyping of single nucleotide polymorphisms (SNPs) for genome-wide association requires technologies for generating millions of genotypes with relative ease but also at a reasonable cost and with high accuracy. In this work, we have developed a theoretical approach to estimate allele frequency in pooled DNA samples, based on the physical principles of DNA immobilization and hybridization on solid surface using the Langmuir kinetic model and quantitative analysis of the allelic signals.</p> <p>Results</p> <p>This method can successfully distinguish allele frequencies differing by 0.01 in the actual pool of clinical samples, and detect alleles with a frequency as low as 2%. The accuracy of measuring known allele frequencies is very high, with the strength of correlation between measured and actual frequencies having an r²= 0.9992. These results demonstrated that this method could allow the accurate estimation of absolute allele frequencies in pooled samples of DNA in a feasible and inexpensive way.</p> <p>Conclusion</p> <p>We conclude that this novel strategy for quantitative analysis of the ratio of SNP allelic sequences in DNA pools is an inexpensive and feasible alternative for detecting polymorphic differences in candidate gene association studies and genome-wide linkage disequilibrium scans.</p

Isotopic and spin selectivity of H_2 adsorbed in bundles of carbon nanotubes

Due to its large surface area and strongly attractive potential, a bundle of carbon nanotubes is an ideal substrate material for gas storage. In addition, adsorption in nanotubes can be exploited in order to separate the components of a mixture. In this paper, we investigate the preferential adsorption of D_2 versus H_2(isotope selectivity) and of ortho versus para(spin selectivity) molecules confined in the one-dimensional grooves and interstitial channels of carbon nanotube bundles. We perform selectivity calculations in the low coverage regime, neglecting interactions between adsorbate molecules. We find substantial spin selectivity for a range of temperatures up to 100 K, and even greater isotope selectivity for an extended range of temperatures,up to 300 K. This isotope selectivity is consistent with recent experimental data, which exhibit a large difference between the isosteric heats of D_2 and H_2 adsorbed in these bundles.Comment: Paper submitted to Phys.Rev. B; 17 pages, 2 tables, 6 figure

The CDEX-1 1 kg Point-Contact Germanium Detector for Low Mass Dark Matter Searches

The CDEX Collaboration has been established for direct detection of light dark matter particles, using ultra-low energy threshold p-type point-contact germanium detectors, in China JinPing underground Laboratory (CJPL). The first 1 kg point-contact germanium detector with a sub-keV energy threshold has been tested in a passive shielding system located in CJPL. The outputs from both the point-contact p+ electrode and the outside n+ electrode make it possible to scan the lower energy range of less than 1 keV and at the same time to detect the higher energy range up to 3 MeV. The outputs from both p+ and n+ electrode may also provide a more powerful method for signal discrimination for dark matter experiment. Some key parameters, including energy resolution, dead time, decay times of internal X-rays, and system stability, have been tested and measured. The results show that the 1 kg point-contact germanium detector, together with its shielding system and electronics, can run smoothly with good performances. This detector system will be deployed for dark matter search experiments.Comment: 6 pages, 8 figure

Phosphonium polymers for gene delivery

Phosphonium salt-containing polymers have very recently started to emerge as attractive materials for the engineering non-viral gene delivery systems. Compared to more frequently utilised ammonium-based polymers, some of these materials can enhance binding of nucleic acid at lower polymer concentration, and mediate good transfections efficiency, with low cytotoxicity. However, for years one of the main hurdles for their widespread application has been the lack of general routes for their synthesis. To date a range of polymerisation techniques have been explored, with the majority of them focussing on radical polymerisation, especially controlled radical polymerisation (CRP) techniques – ATRP, NMP and RAFT polymerisation - both by polymerisation of phosphonium monomers or by post-polymerisation modification of polymer intermediates. This review article aims at discussing key differences and similarities between phosphonium-and other analogous cations, how these affect binding to polynucleotides, and will provide an overview of the phosphonium polymer systems that have been utilised for gene delivery