ABSTRACT Artificial metalloenzymes (ArMs) exhibit exceptional selectivity, yet extending their reactivity beyond native cofactors remains a major challenge. While previous designs using native protein scaffolds to incorporate nonnative cofactors have been reported, de novo protein design enables tailored scaffolds that...
Jing-Xiang Wang, Yun-Ling Deng, Indrek Kalvet et al.· Angewandte Chemie· 0 citations
Phagocytic synapse enhancers are developed, a class of modular immune engagers comprising a high-affinity PD-L1 binder coupled to a macrophage-stimulating peptide, tuftsin, that provides a blueprint for a plug-and-play platform of immune engagers targeting diverse cancer-associated pathways.
Valerio Sabatino, Cong Tang, Rita C. Acúrcio et al.· Cancer Research· 0 citations
Irreversible covalent inhibitors have garnered significant attention in recent years. Despite encouraging progress, the vast majority contain electrophiles that target the least abundant amino acid cysteine, substantially limiting target inhibitor design for therapeutic intervention. Here, we generalize 2-ethynylbenzal...
Paul M. Levine, Patrick W. Erickson, Timothy W. Craven et al.· ACS Chemical Biology· 0 citations
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