Microstructure and corrosion evolution of additively manufactured aluminium alloy AA7075 as a function of ageing

Additively manufactured high strength aluminium alloy AA7075 was prepared using selective laser melting. High strength aluminium alloys prepared by selective laser melting have not been widely studied to date. The evolution of microstructure and hardness, with the attendant corrosion, were investigated. Additively manufactured AA7075 was investigated both in the as-produced condition and as a function of artificial ageing. The microstructure of specimens prepared was studied using electron microscopy. Production of AA7075 by selective laser melting generated a unique microstructure, which was altered by solutionising and further altered by artificial ageing - resulting in microstructures distinctive to that of wrought AA7075-T6. The electrochemical response of additively manufactured AA7075 was dependent on processing history, and unique to wrought AA7075-T6, whereby dissolution rates were generally lower for additively manufactured AA7075. Furthermore, immersion exposure testing followed by microscopy, indicated different corrosion morphology for additively manufactured AA7075, whereby resultant pit size was notably smaller, in contrast to wrought AA7075-T6.Comment: 37 pages, includes 4 Tables and 11 Figure

ASSESSING TARGET SPECIFICITY OF THE SMALL MOLECULE INHIBITOR MARIMASTAT TO SNAKE VENOM TOXINS: A NOVEL APPLICATION OF THERMAL PROTEOME PROFILING

New treatments that circumvent the pitfalls of traditional antivenom therapies are critical to address the problem of snakebite globally. Numerous snake venom toxin inhibitors have shown promising cross-species neutralization of medically significant venom toxins in vivo and in vitro. The development of high-throughput approaches for the screening of such inhibitors could accelerate their identification, testing, and implementation, and thus holds exciting potential for improving the treatments and outcomes of snakebite envenomation worldwide. Energetics-based proteomic approaches, including Thermal Proteome Profiling (TPP) and Proteome Integral Solubility Alteration (PISA) assays, represent “deep proteomics” methods for high throughput, proteome-wide identification of drug targets and ligands. In the following study, we apply TPP and PISA methods to characterize the interactions between venom toxin proteoforms in Crotalus atrox (Western Diamondback Rattlesnake) and the snake venom metalloprotease (SVMP) inhibitor marimastat. We investigate its venom proteome-wide effects and characterize its interactions with specific SVMP proteoforms, as well as its potential targeting of non-SVMP venom toxin families. We also compare the performance of PISA thermal window and soluble supernatant with insoluble precipitate using two inhibitor concentrations, providing the first demonstration of the utility of a sensitive high-throughput PISA-based approach to assess the direct targets of small molecule inhibitors for snake venom