An Approximation for the rp-Process

Hot (explosive) hydrogen burning or the Rapid Proton Capture Process (rp-process) occurs in a number of astrophysical environments. Novae and X-ray bursts are the most prominent ones, but accretion disks around black holes and other sites are candidates as well. The expensive and often multidimensional hydro calculations for such events require an accurate prediction of the thermonuclear energy generation, while avoiding full nucleosynthesis network calculations. In the present investigation we present an approximation scheme applicable in a temperature range which covers the whole range of all presently known astrophysical sites. It is based on the concept of slowly varying hydrogen and helium abundances and assumes a kind of local steady flow by requiring that all reactions entering and leaving a nucleus add up to a zero flux. This scheme can adapt itself automatically and covers situations at low temperatures, characterized by a steady flow of reactions, as well as high temperature regimes where a $(p,\gamma)-(\gamma,p)$-equilibrium is established. In addition to a gain of a factor of 15 in computational speed over a full network calculation, and an energy generation accurate to more than 15 %, this scheme also allows to predict correctly individual isotopic abundances. Thus, it delivers all features of a full network at a highly reduced cost and can easily be implemented in hydro calculations.Comment: 18 pages, LaTeX using astrobib and aas2pp4, includes PostScript figures; Astrophysical Journal, in press. PostScript source also available at http://quasar.physik.unibas.ch/preps.htm

Aerosolized adenovirus-vectored vaccine as an alternative vaccine delivery method

Conventional parenteral injection of vaccines is limited in its ability to induce locally-produced immune responses in the respiratory tract, and has logistical disadvantages in widespread vaccine administration. Recent studies suggest that intranasal delivery or vaccination in the respiratory tract with recombinant viral vectors can enhance immunogenicity and protection against respiratory diseases such as influenza and tuberculosis, and can offer more broad-based generalized protection by eliciting durable mucosal immune responses. Controlled aerosolization is a method to minimize vaccine particle size and ensure delivery to the lower respiratory tract. Here, we characterize the dynamics of aerosolization and show the effects of vaccine concentration on particle size, vector viability, and the actual delivered dose of an aerosolized adenoviral vector. In addition, we demonstrate that aerosol delivery of a recombinant adenoviral vaccine encoding H1N1 hemagglutinin is immunogenic and protects ferrets against homologous viral challenge. Overall, aerosol delivery offers comparable protection to intramuscular injection, and represents an attractive vaccine delivery method for broad-based immunization campaigns

Stringency of the 2-His–1-Asp Active-Site Motif in Prolyl 4-Hydroxylase

The non-heme iron(II) dioxygenase family of enzymes contain a common 2-His–1-carboxylate iron-binding motif. These enzymes catalyze a wide variety of oxidative reactions, such as the hydroxylation of aliphatic C–H bonds. Prolyl 4-hydroxylase (P4H) is an α-ketoglutarate-dependent iron(II) dioxygenase that catalyzes the post-translational hydroxylation of proline residues in protocollagen strands, stabilizing the ensuing triple helix. Human P4H residues His412, Asp414, and His483 have been identified as an iron-coordinating 2-His–1-carboxylate motif. Enzymes that catalyze oxidative halogenation do so by a mechanism similar to that of P4H. These halogenases retain the active-site histidine residues, but the carboxylate ligand is replaced with a halide ion. We replaced Asp414 of P4H with alanine (to mimic the active site of a halogenase) and with glycine. These substitutions do not, however, convert P4H into a halogenase. Moreover, the hydroxylase activity of D414A P4H cannot be rescued with small molecules. In addition, rearranging the two His and one Asp residues in the active site eliminates hydroxylase activity. Our results demonstrate a high stringency for the iron-binding residues in the P4H active site. We conclude that P4H, which catalyzes an especially demanding chemical transformation, is recalcitrant to change

Nuclear uncertainties in the NeNa-MgAl cycles and production of 22Na and 26Al during nova outbursts

Classical novae eject significant amounts of nuclear processed material into the interstellar medium. Among the isotopes synthesized during such explosions, two radioactive nuclei deserve a particular attention: 22Na and 26Al. In this paper, we investigate the nuclear paths leading to 22Na and 26Al production during nova outbursts by means of an implicit, hydrodynamic code that follows the course of the thermonuclear runaway from the onset of accretion up to the ejection stage. New evolutionary sequences of ONe novae have been computed, using updated nuclear reaction rates relevant to 22Na and 26Al production. Special attention is focused on the role played by nuclear uncertainties within the NeNa and MgAl cycles in the synthesis of such radioactive species. From the series of hydrodynamic models, which assume upper, recommended or lower estimates of the reaction rates, we derive limits on the production of both 22Na and 26Al. We outline a list of nuclear reactions which deserve new experimental investigations in order to reduce the wide dispersion introduced by nuclear uncertainties in the 22Na and 26Al yields.Comment: 46 pages, 4 figures. Accepted for publication in The Astrophysical Journa

Sensitivity of p-Process Nucleosynthesis to Nuclear Reaction Rates in a 25 Solar Mass Supernova Model

The astrophysical p process, which is responsible for the origin of the proton rich stable nuclei heavier than iron, was investigated using a full nuclear reaction network for a type II supernova explosion when the shock front passes through the O/Ne layer. Calculations were performed with a multi-layer model adopting the seed of a pre-explosion evolution of a 25 solar mass star. The reaction flux was calculated to determine the main reaction path and branching points responsible for synthesizing the proton rich nuclei. In order to investigate the impact of nuclear reaction rates on the predicted p-process abundances, extensive simulations with different sets of collectively and individually modified neutron-, proton-, alpha-capture and photodisintegration rates have been performed. These results are not only relevant to explore the nuclear physics related uncertainties in p-process calculations but are also important for identifying the strategy and planning of future experiments.Comment: 27 pages, 24 figures, accepted for publication in ApJ

Comparative Efficacy of Hemagglutinin, Nucleoprotein, and Matrix 2 Protein Gene-Based Vaccination against H5N1 Influenza in Mouse and Ferret

Efforts to develop a broadly protective vaccine against the highly pathogenic avian influenza A (HPAI) H5N1 virus have focused on highly conserved influenza gene products. The viral nucleoprotein (NP) and ion channel matrix protein (M2) are highly conserved among different strains and various influenza A subtypes. Here, we investigate the relative efficacy of NP and M2 compared to HA in protecting against HPAI H5N1 virus. In mice, previous studies have shown that vaccination with NP and M2 in recombinant DNA and/or adenovirus vectors or with adjuvants confers protection against lethal challenge in the absence of HA. However, we find that the protective efficacy of NP and M2 diminishes as the virulence and dose of the challenge virus are increased. To explore this question in a model relevant to human disease, ferrets were immunized with DNA/rAd5 vaccines encoding NP, M2, HA, NP+M2 or HA+NP+M2. Only HA or HA+NP+M2 vaccination conferred protection against a stringent virus challenge. Therefore, while gene-based vaccination with NP and M2 may provide moderate levels of protection against low challenge doses, it is insufficient to confer protective immunity against high challenge doses of H5N1 in ferrets. These immunogens may require combinatorial vaccination with HA, which confers protection even against very high doses of lethal viral challenge

Research on Fundamental Breach of Contract:from the perspective of CISG

根本违约是从英国法中产生的一种违约形态，被《联合国国际货物销售合同公约》采纳后成为一个国际性的条款。根本违约制度在《公约》中具有极为重要的地位，扮演了中心的角色。一般认为，根本违约是合同当事人违反了合同中最重要、根本性的条款而构成的违约，另一方当事人不仅有权要求损害赔偿，更重要的是有权宣告合同无效（解除合同）的制度。我国《合同法》第94条也规定了根本违约制度。本文对《公约》的根本违约制度进行了较为全面、深入的分析探讨，指出了我国《合同法》根本违约制度的缺陷并提出了改进的建议。全文除前言和结语外，正文共分为四章：第一章：根本违约制度之国际概览。本章以宏观的角度介绍了根本违约制度在英美法和大陆法两...The mechanism of fundamental breach of contract was derived from British law and adopted by CISG, and had then been developed into an international term. This mechanism plays an extremely important role in CISG. Generally, the mechanism is invoked where one party violates the most important and fundamental terms of the contract and the other party thus has the right to claim damages and to declare...学位：法学硕士院系专业：法学院法律系_国际法学(含国际公法、国际私法、国际经济法)学号：20040810

Investigation of the 19Na via resonance elastic scattering

The structure of the unbound proton-rich isotope 19Na was studied in resonance elastic scattering of a radioactive 18Ne beam on a proton target using the thick-target inverse-kinematics method. The experiment covered excitation energy range from 0.5 to 2.7 MeV in c.m.s. Only one state of 19Na (the second excited state) was observed. A combined R-matrix and potential-model analysis was performed. The spin and parity assignment of this second excited state was confirmed to be 1/2+. We showthat the position of the 1/2+ state significantly affects the reaction rate through that state but the total reaction rate remains unchanged since the 18Ne(2p,gamma) proceeds mostly via the ground and first excited states in 19Na at stellar temperatures.Comment: 13 pages, 5 figure

Asparagine hydroxylation is a reversible post-translational modification

Amino acid hydroxylation is a common post-translational modification, which generally regulates protein interactions or adds a functional group that can be further modified. Such hydroxylation is currently considered irreversible, necessitating the degradation and re-synthesis of the entire protein to reset the modification. Here we present evidence that the cellular machinery can reverse FIH-mediated asparagine hydroxylation on intact proteins. These data suggest that asparagine hydroxylation is a flexible and dynamic post-translational modification akin to modifications involved in regulating signaling networks, such as phosphorylation, methylation and ubiquitylation