147 research outputs found

    The Bourke lock and weir

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    Pseudomonas aeruginosa PilY1 Binds Integrin in an RGD- and Calcium-Dependent Manner

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    PilY1 is a type IV pilus (tfp)-associated protein from the opportunistic pathogen Pseudomonas aeruginosa that shares functional similarity with related proteins in infectious Neisseria and Kingella species. Previous data have shown that PilY1 acts as a calcium-dependent pilus biogenesis factor necessary for twitching motility with a specific calcium binding site located at amino acids 850–859 in the 1,163 residue protein. In addition to motility, PilY1 is also thought to play an important role in the adhesion of P. aeruginosa tfp to host epithelial cells. Here, we show that PilY1 contains an integrin binding arginine-glycine-aspartic acid (RGD) motif located at residues 619–621 in the PilY1 from the PAK strain of P. aeruginosa; this motif is conserved in the PilY1s from the other P. aeruginosa strains of known sequence. We demonstrate that purified PilY1 binds integrin in vitro in an RGD-dependent manner. Furthermore, we identify a second calcium binding site (amino acids 600–608) located ten residues upstream of the RGD. Eliminating calcium binding from this site using a D608A mutation abolished integrin binding; in contrast, a calcium binding mimic (D608K) preserved integrin binding. Finally, we show that the previously established PilY1 calcium binding site at 851–859 also impacts the protein's association with integrin. Taken together, these data indicate that PilY1 binds to integrin in an RGD- and calcium-dependent manner in vitro. As such, P. aeruginosa may employ these interactions to mediate host epithelial cell binding in vivo

    Remediation of radioiodine using polyamine anion exchange resins

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    Two weak base anion exchange resins, Lewatit A365 and Purolite MTS9850, have been tested for the removal of aqueous iodide from conditions simulating nuclear waste reprocessing streams. pH variation and relevant co-contaminant addition (nitrate, molybdate and iodine) allowed for assessment of iodide extraction behaviour of each resin. Isotherm experiments were performed and maximum uptake capacities obtained exceed current industrial adsorbents, such as silver-impregnated zeolites. Maximum loading capacities, determined by Dubinin–Radushkevich isotherm, were 761 ± 14 mg g−1 for MTS9850 and 589 ± 15 mg g−1 for A365. Uptake for both resins was significantly suppressed by nitrate and molybdate ions. The presence of dissolved iodine in the raffinate however, was found to increase iodide uptake. This was explained by characterisation of the spent resin surface by infrared and Raman spectroscopy, which determined the presence of triiodide, indicating charge-transfer complex formation on the surface. Dynamic studies assessed the effect of co-contaminants on iodide uptake in a column environment. Data was fitted to three dynamic models, with the Dose-Response model providing the best description of breakthrough. In all cases iodide breakthrough was accelerated, indicating suppression of uptake, but capacity was still significant
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