135 research outputs found

    Gravitational intraction on quantum level and consequences thereof

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    The notion of gravitational emission as an emission of the same level with electromagnetic emission is based on the proven fact of existence of electrons stationary states in its own gravitational field, characterized by gravitational constantComment: 22 pages, 9 figure

    Computational modeling of pulsed-power-driven magnetized target fusion experiments

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    Direct magnetic drive using electrical pulsed power has been considered impractically slow for traditional inertial confinement implosion of fusion targets. However, if the target contains a preheated, magnetized plasma, magnetothermal insulation may allow the near-adiabatic compression of such a target to fusion conditions on a much slower time scale. 100-MJ-class explosive flux compression generators with implosion kinetic energies far beyond those available with conventional fusion drivers, are an inexpensive means to investigate such magnetized target fusion (MTF) systems. One means of obtaining the preheated and magnetized plasma required for an MTF system is the recently reported {open_quotes}MAGO{close_quotes} concept. MAGO is a unique, explosive-pulsed-power driven discharge in two cylindrical chambers joined by an annular nozzle. Joint Russian-American MAGO experiments have reported D-T neutron yields in excess of 10{sup 13} from this plasma preparation stage alone, without going on to the proposed separately driven NM implosion of the main plasma chamber. Two-dimensional MED computational modeling of MAGO discharges shows good agreement to experiment. The calculations suggest that after the observed neutron pulse, a diffuse Z-pinch plasma with temperature in excess of 100 eV is created, which may be suitable for subsequent MTF implosion, in a heavy liner magnetically driven by explosive pulsed power. Other MTF concepts, such as fiber-initiated Z-pinch target plasmas, are also being computationally and theoretically evaluated. The status of our modeling efforts will be reported

    Adaptation of a transmitted/founder simian-human immunodeficiency virus for enhanced replication in rhesus macaques

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    Transmitted/founder (TF) simian-human immunodeficiency viruses (SHIVs) express HIV-1 envelopes modified at position 375 to efficiently infect rhesus macaques while preserving authentic HIV-1 Env biology. SHIV.C.CH505 is an extensively characterized virus encoding the TF HIV-1 Env CH505 mutated at position 375 shown to recapitulate key features of HIV-1 immunobiology, including CCR5-tropism, a tier 2 neutralization profile, reproducible early viral kinetics, and authentic immune responses. SHIV.C.CH505 is used frequently in nonhuman primate studies of HIV, but viral loads after months of infection are variable and typically lower than those in people living with HIV. We hypothesized that additional mutations besides Δ375 might further enhance virus fitness without compromising essential components of CH505 Env biology. From sequence analysis of SHIV.C.CH505-infected macaques across multiple experiments, we identified a signature of envelope mutations associated with higher viremia. We then used short-term in vivo mutational selection and competition to identify a minimally adapted SHIV.C.CH505 with just five amino acid changes that substantially improve virus replication fitness in macaques. Next, we validated the performance of the adapted SHIV in vitro and in vivo and identified the mechanistic contributions of selected mutations. In vitro, the adapted SHIV shows improved virus entry, enhanced replication on primary rhesus cells, and preserved neutralization profiles. In vivo, the minimally adapted virus rapidly outcompetes the parental SHIV with an estimated growth advantage of 0.14 days-1 and persists through suppressive antiretroviral therapy to rebound at treatment interruption. Here, we report the successful generation of a well-characterized, minimally adapted virus, termed SHIV.C.CH505.v2, with enhanced replication fitness and preserved native Env properties that can serve as a new reagent for NHP studies of HIV-1 transmission, pathogenesis, and cure
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