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Kawai Y, Garduo L, Theodore M, Yang J, Arinze IJ
Using in silico design, structureactivity relationships (SARs), chemical optimization, cell-based assays and in vivo experiments, we identified and characterized the first-in-kind small-molecule inhibitors of STX7Munc13-4-dependent endosomal maturation and signaling for use in immune cells that contribute to systemic inflammation
Furthermore, both evolved proteases initiated cell death when reconstituted with BoNTs H N domain, enabling self-delivery into cancer cells
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