495 research outputs found

    Consistent Anisotropic Repulsions for Simple Molecules

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    We extract atom-atom potentials from the effective spherical potentials that suc cessfully model Hugoniot experiments on molecular fluids, e.g., O2O_2 and N2N_2. In the case of O2O_2 the resulting potentials compare very well with the atom-atom potentials used in studies of solid-state propertie s, while for N2N_2 they are considerably softer at short distances. Ground state (T=0K) and room temperatu re calculations performed with the new N−NN-N potential resolve the previous discrepancy between experimental and theoretical results.Comment: RevTeX, 5 figure

    BICEP3: a 95 GHz refracting telescope for degree-scale CMB polarization

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    BICEP3 is a 550 mm-aperture refracting telescope for polarimetry of radiation in the cosmic microwave background at 95 GHz. It adopts the methodology of BICEP1, BICEP2 and the Keck Array experiments - it possesses sufficient resolution to search for signatures of the inflation-induced cosmic gravitational-wave background while utilizing a compact design for ease of construction and to facilitate the characterization and mitigation of systematics. However, BICEP3 represents a significant breakthrough in per-receiver sensitivity, with a focal plane area 5×\times larger than a BICEP2/Keck Array receiver and faster optics (f/1.6f/1.6 vs. f/2.4f/2.4). Large-aperture infrared-reflective metal-mesh filters and infrared-absorptive cold alumina filters and lenses were developed and implemented for its optics. The camera consists of 1280 dual-polarization pixels; each is a pair of orthogonal antenna arrays coupled to transition-edge sensor bolometers and read out by multiplexed SQUIDs. Upon deployment at the South Pole during the 2014-15 season, BICEP3 will have survey speed comparable to Keck Array 150 GHz (2013), and will significantly enhance spectral separation of primordial B-mode power from that of possible galactic dust contamination in the BICEP2 observation patch.Comment: 12 pages, 5 figures. Presented at SPIE Astronomical Telescopes and Instrumentation 2014: Millimeter, Submillimeter, and Far-Infrared Detectors and Instrumentation for Astronomy VII. To be published in Proceedings of SPIE Volume 915

    DNA-Interactive Properties of Crotamine, a Cell-Penetrating Polypeptide and a Potential Drug Carrier

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    Crotamine, a 42-residue polypeptide derived from the venom of the South American rattlesnake Crotalus durissus terrificus, has been shown to be a cell-penetrating protein that targets chromosomes, carries plasmid DNA into cells, and shows specificity for actively proliferating cells. Given this potential role as a nucleic acid-delivery vector, we have studied in detail the binding of crotamine to single- and double-stranded DNAs of different lengths and base compositions over a range of ionic conditions. Agarose gel electrophoresis and ultraviolet spectrophotometry analysis indicate that complexes of crotamine with long-chain DNAs readily aggregate and precipitate at low ionic strength. This aggregation, which may be important for cellular uptake of DNA, becomes less likely with shorter chain length. 25-mer oligonucleotides do not show any evidence of such aggregation, permitting the determination of affinities and size via fluorescence quenching experiments. The polypeptide binds non-cooperatively to DNA, covering about 5 nucleotide residues when it binds to single (ss) or (ds) double stranded molecules. The affinities of the protein for ss-vs. ds-DNA are comparable, and inversely proportional to salt levels. Analysis of the dependence of affinity on [NaCl] indicates that there are a maximum of,3 ionic interactions between the protein and DNA, with some of the binding affinity attributable to non-ionic interactions. Inspection of the three-dimensional structure of the protein suggests that residues 31 to 35, Arg-Trp-Arg-Trp-Lys, could serve as a potential DNA-binding site. A hexapeptide containing this sequence displayed a lower DNA binding affinity and salt dependence as compared to the full-length protein, likely indicative of a more suitable 3D structure and the presence of accessory binding sites in the native crotamine. Taken together, the data presented here describing crotamine-DNA interactions may lend support to the design of more effective nucleic acid drug delivery vehicles which take advantage of crotamine as a carrier with specificity for actively proliferating cells. Citation: Chen P-C, Hayashi MAF, Oliveira EB, Karpel RL (2012) DNA-Interactive Properties of Crotamine, a Cell-Penetrating Polypeptide and a Potential Drug Carrier. PLoS ONE 7(11): e48913. doi:10.1371/journal.pone.0048913University of Maryland Baltimore County Designated Research Initiative Fund, an Undergraduate Research AwardUniversity of Maryland Baltimore County Designated Research Initiative Fund, an Undergraduate Research AwardFundao de Amparo a Pesquisa do Estado de So Paulo [FAPESP]Fundao de Amparo a Pesquisa do Estado de So PauloNational Council of Technological and Scientific Development [CNPq]National Council of Technological and Scientific Developmen

    BICEP2 / Keck Array VIII: Measurement of gravitational lensing from large-scale B-mode polarization

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    We present measurements of polarization lensing using the 150 GHz maps which include all data taken by the BICEP2 & Keck Array CMB polarization experiments up to and including the 2014 observing season (BK14). Despite their modest angular resolution (∼0.5∘\sim 0.5^\circ), the excellent sensitivity (∼3μ\sim 3\muK-arcmin) of these maps makes it possible to directly reconstruct the lensing potential using only information at larger angular scales (ℓ≤700\ell\leq 700). From the auto-spectrum of the reconstructed potential we measure an amplitude of the spectrum to be ALϕϕ=1.15±0.36A^{\phi\phi}_{\rm L}=1.15\pm 0.36 (Planck Λ\LambdaCDM prediction corresponds to ALϕϕ=1A^{\phi\phi}_{\rm L}=1), and reject the no-lensing hypothesis at 5.8σ\sigma, which is the highest significance achieved to date using an EB lensing estimator. Taking the cross-spectrum of the reconstructed potential with the Planck 2015 lensing map yields ALϕϕ=1.13±0.20A^{\phi\phi}_{\rm L}=1.13\pm 0.20. These direct measurements of ALϕϕA^{\phi\phi}_{\rm L} are consistent with the Λ\LambdaCDM cosmology, and with that derived from the previously reported BK14 B-mode auto-spectrum (ALBB=1.20±0.17A^{\rm BB}_{\rm L}=1.20\pm 0.17). We perform a series of null tests and consistency checks to show that these results are robust against systematics and are insensitive to analysis choices. These results unambiguously demonstrate that the B-modes previously reported by BICEP / Keck at intermediate angular scales (150≲ℓ≲350150\lesssim\ell\lesssim 350) are dominated by gravitational lensing. The good agreement between the lensing amplitudes obtained from the lensing reconstruction and B-mode spectrum starts to place constraints on any alternative cosmological sources of B-modes at these angular scales.Comment: 12 pages, 8 figure
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