Magnon Heat Transport in (Sr,La)_14Cu_24O_41

We have measured the thermal heat conductivity kappa of the compounds Sr_14Cu_24O_41 and Ca_9La_5Cu_24O_41 containing doped and undoped spin ladders, respectively. We find a huge anisotropy of both, the size and the temperature dependence of kappa which we interpret in terms of a very large heat conductivity due to the magnetic excitations of the one-dimensional spin ladders. This magnon heat conductivity decreases with increasing hole doping of the ladders. The magnon heat transport is analyzed theoretically using a simple kinetic model. From this analysis we determine the spin gap and the temperature dependent mean free path of the magnons which ranges by several thousand angstroms at low temperature. The relevance of several scattering channels for the magnon transport is discussed.Comment: 6 pages, 5 figures, submitted to Phys. Rev.

Validation of a cell-based ELISA as a screening tool identifyinganti-alphavirus small-molecule inhibitors

Venezuelan (VEEV), eastern, and western equine encephalitis viruses, members of the genus Alphavirus, are causative agents of debilitative and sometimes fatal encephalitis. Although human cases are rare, these viruses pose a threat to military personnel, and to public health, due to their potential use as bioweapons. Currently, there are no licensed therapeutics for treating alphavirus infections. To address this need, small-molecules with potential anti-alphavirus activity, provided by collaborators, are tested routinely in live alpha virus assays utilizing time-consuming virus yield-reduction assays. To expedite the screening/hit-confirmation process, a cell-based enzyme-linked immunosorbent assay (ELISA) was developed and validated for the measurement of VEEV infection. A signal-to-background ratio of \u3e900,and a z-factor of \u3e0.8 indicated the robustness of this assay. For validation, the cell-based ELISA was compared directly to results from virus yield reduction assays in a single dose screen of 21 compounds. Using stringent criteria for anti-VEEV activity there was 90% agreement between the two assays (compounds displaying either antiviral activity, or no effect, in both assays). A concurrent compound-induced cell toxicity assay effectively filtered out false-positive hits. The cell-based ELISA also reproduced successfully compound dose–response virus inhibition data observed using the virus yield reduction assay. With available antibodies, this assay can be adapted readily to other viruses of interest to the biodefense community. Additionally, it is cost-effective, rapid, and amenable to automation and scale-up. There-fore, this assay could expedite greatly screening efforts and the identification of effective anti-alpha virus inhibitors