An Investigation of the Adsorption Characteristics of 5'ATP and 5'AMP onto the Surface of Caso4 x 2H2O

A model has been proposed in which solid surfaces can act as a site for cataletic activity of condensation reactions for certain biomolecules. From this model, the adsorption characteristics of 5'ATP and 5'AMP onto the surface of CaSO4.2H2O was chosen for study. It has been proven that 5'ATP and 5'AMP do adsorb onto the surface of CaSO4. Studies were then made to determine the dependence of absorption versus time, concentration, ionic strength and pH. It was found that the adsorption of the nucleotides is highly pH dependent, primarily determined by the phosphate acid groups of the nucleic acid molecule. From this investigation, the data obtained is discussed in relation to the model for the prebiotic earth

An investigation of the adsorption characteristics of 5 prime ATP and 5 prime AMP onto the surface of CaSO sub 4 x 2H sub 2 O

A model has been proposed (Lahev and Chans, 1982) in which solid surfaces can act as a site for catalytic activity of condensation reactions for certain biomolecules. From this model, the adsorption characteristics of 5'ATP and 5'AMP onto the surface of CaSO4 2H2O was chosen for study. It has been proven that 5'ATP and 5'AMP do adsorb onto the surface of CaSO4. Studies were then made to determine the dependence of adsorption versus time, concentration, ionic strength and pH. It was found that the adsorption of the nucleotides is highly pH dependent, primarily determined by the phosphate acid groups of the nucleic acid molecule. From this investigation, the data obtained are discussed in relation to the model for the prebiotic earth

Leptonic and Hadronic Modeling of Fermi-Detected Blazars

We describe new implementations of leptonic and hadronic models for the broadband emission from relativistic jets in AGN in a temporary steady state. For the leptonic model, a temporary equilibrium between particle injection/acceleration, radiative cooling, and escape from a spherical emission region is evaluated, and the self-consistent radiative output is calculated. For the hadronic model, a temporary equilibrium between particle injection/acceleration, radiative and adiabatic cooling, and escape is evaluated for both primary electrons and protons. A new, semi-analytical method to evaluate the radiative output from cascades initiated by internal gamma-gamma pair production is presented. We use our codes to fit snap-shot spectral energy distributions of a representative set of Fermi-LAT detected blazars. We find that the leptonic model provides acceptable fits to the SEDs of almost all blazars with parameters close to equipartition between the magnetic field and the relativistic electron population. However, the hard gamma-ray spectrum of AO 0235+164, in contrast to the very steep IR-optical-UV continuum, poses a severe problem for the leptonic model. If charge neutrality in leptonic models is provided by cold protons, the kinetic energy carried by the jet should be dominated by protons. We find satisfactory representations of the snapshot SEDs of most blazars in our sample with the hadronic model presented here. However, in the case of two quasars the characteristic break at a few GeV energies can not be well modelled. All of our hadronic model fits require powers in relativistic protons in the range L_p ~ 1e47 - 1e49 erg/s.Comment: Accepted for Publication in The Astrophysical Journa

Rapid and efficient stable gene transfer to mesenchymal stromal cells using a modified foamy virus vector

Mesenchymal stromal cells (MSCs) hold great promise for regenerative medicine. Stable ex vivo gene transfer to MSCs could improve the outcome and scope of MSC therapy, but current vectors require multiple rounds of transduction, involve genotoxic viral promoters and/or the addition of cytotoxic cationic polymers in order to achieve efficient transduction. We describe a self-inactivating foamy virus vector (FVV), incorporating the simian macaque foamy virus envelope and using physiological promoters, which efficiently transduces murine MSCs (mMSCs) in a single-round. High and sustained expression of the transgene, whether GFP or the lysosomal enzyme, arylsulphatase A (ARSA), was achieved. Defining MSC characteristics (surface marker expression and differentiation potential), as well as long-term engraftment and distribution in the murine brain following intracerebroventricular delivery, are unaffected by FVV transduction. Similarly, greater than 95% of human MSCs (hMSCs) were stably transduced using the same vector, facilitating human application. This work describes the best stable gene transfer vector available for mMSCs and hMSCs