THE REPAIR OF DNA STRAND BREAKS IN HUMAN LYMPHOCYTES EXPOSED TO NEAR UV-RADIATION (UVA) AND FAR UV-RADIATION (UVC)

Abstract— UVA irradiation of human lymphocytes induces DNA strand breaks and a portion of these breaks are closed at a slower rate than X-ray induced DNA strand breaks and the strand breaks generated during repair of UVC induced DNA lesions. In addition, the yield of DNA strand breaks in lymphocytes pretreated with UVA radiation and given a subsequent exposure with UVC radiation is higher and shows a slower decrease with increasing repair time in comparison with the expected yield based on additivity between UVA and UVC induced DNA strand breaks. This indicates that UVA delays the closure of the intermediate strand breaks formed in the repair process of UVC induced DNA lesions.     

Surface modification of hydroxyapatite to avoid bacterial adhesion

Hydroxyapatite was surface-modified by adsorption of nonionic polymers carrying phosphate groups as anchoring groups. A combination of alcohol ethoxylate and alkyl phosphate was also used. The possibility of interfering with early microbial colonization on apatite, mimicking the tooth surface, was investigated using radiolabelledStreptococcus mutans as model bacteria. The polymers, a nonionic cellulose ether and an EO/PO block copolymer based on polyglycerol as starting alcohol, were effective in buffer but gave only limited reduction of bacterial adhesion when the apatite had been pretreated with saliva. A 11 molar mixture of alcohol ethoxylate and alkyl phosphate was effective both with and without saliva, however. Studies with¹⁴C-labeled compounds, as well as microelectrophoresis experiments, indicate that an unsymmetrical double layer is formed on the apatite surface with predominantly alkyl phosphate in the inner layer and with alcohol ethoxylate pointing towards the water phase.     

The asymptotic distributions of generalized U-statistics with applications to random graphs

We consider the random variable

Evolution of blast wave profiles in simulated air blasts: experiment and computational modeling

Shock tubes have been extensively used in the study of blast traumatic brain injury due to increased incidence of blast-induced neurotrauma in Iraq and Afghanistan conflicts. One of the important aspects in these studies is how to best replicate the field conditions in the laboratory which relies on reproducing blast wave profiles. Evolution of the blast wave profiles along the length of the compression-driven air shock tube is studied using experiments and numerical simulations with emphasis on the shape and magnitude of pressure time profiles. In order to measure dynamic pressures of the blast, a series of sensors are mounted on a cylindrical specimen normal to the flow direction. Our results indicate that the blast wave loading is significantly different for locations inside and outside of the shock tube. Pressure profiles inside the shock tube follow the Friedlander waveform fairly well. Upon approaching exit of the shock tube, an expansion wave released from the shock tube edges significantly degrades the pressure profiles. For tests outside the shock tube, peak pressure and total impulse reduce drastically as we move away from the exit and majority of loading is in the form of subsonic jet wind. In addition, the planarity of the blast wave degrades as blast wave evolves three dimensionally. Numerical results visually and quantitatively confirm the presence of vortices, jet wind and three-dimensional expansion of the planar blast wave near the exit. Pressure profiles at 90° orientation show flow separation. When cylinder is placed inside, this flow separation is not sustained, but when placed outside the shock tube this flow separation is sustained which causes tensile loading on the sides of the cylinder. Friedlander waves formed due to field explosives in the intermediate-to far-field ranges are replicated in a narrow test region located deep inside the shock tube.     

Lipopolysaccharide removal by a peptide-functionalized surface

Five peptides: BPI(85-109); CAP18(106-137); endotoxin inhibitor (EI); GQ33 and GQ33C, derived from lipopolysaccharide (LPS)-binding molecules were investigated for LPS-binding ability with a view to a potential use in extracorporeal therapy. The surface plasmon resonance technique (SPR) was used to monitor the interaction between LPS in solution and the surface-immobilized peptides. The peptides were covalently bound to a model dextran surface via inherent amino groups or via terminally introduced cysteine residues. The results showed that the binding efficacy and binding stability of the peptides varied greatly. The CAP18(106-137) peptide, which exhibited the highest binding efficacy and binding stability, was also immobilized on a poly(ethylene imine)-poly(ethylene glycol) (PEI-PEG) surface through maleimide-terminal PEG. The binding efficacy of the CAP18(106-137) peptide was not significantly affected by the different immobilization methods used in the attachment to a dextran or a PEI-PEG surface. LPS bound selectively to CAP18(106-137) and showed very low unspecific binding to the PEI-PEG surface layer. The EI peptide proved to have a reasonably good binding capacity but a less stable interaction with LPS. The other peptides exhibited much poorer binding efficacy. We believe that the results presented in this work can be of practical value for the development of extracorporeal treatment of patients suffering from septic shock.     

Poisson approximation for large deviations

Upper and lower bounds are given for P(S ≤ k), 0 ≤ k ≤ ES, where S is a sum of indicator variables with a special structure, which appears, for example, in subgraph counts in random graphs. in typical cases, these bounds are close to the corresponding probabilities for a Poisson distribution with the same mean as S. There are no corresponding general bounds for P(S ≥ k), k > ES, but some partial results are given.