2023
DOI: 10.1021/jacs.3c05153
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Catalytic Materials Enabled by a Programmable Assembly of Synthetic Polymers and Engineered Bacterial Spores

Abstract: Natural biological materials are formed by self-assembly processes and catalyze a myriad of reactions. Here, we report a programmable molecular assembly of designed synthetic polymers with engineered bacterial spores. This self-assembly process is driven by dynamic covalent bond formation on spore surface glycan and yields macroscopic materials that are structurally stable, self-healing, and recyclable. Molecular programming of polymer species shapes the physical properties of these materials while metabolical… Show more

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Cited by 7 publications
(1 citation statement)
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“…Functional components-anchored cell platforms have emerged as versatile tools for targeting a variety of lesions, such as engineered immune cells, stem cells, tumor cells, bacteria, and platelets. Macrophages (Mø) is a type of phagocytes with strong migratory properties to remove foreign debris and cells from an injury site. When the tissue becomes infected or damaged, inflammatory monocytes’ CC chemokines 2 (CCR2) interact with monocyte chemotactic protein (MCP-1), causing mononuclear cells to differentiate into macrophages and migrate to the injured area . Engineered macrophages have shown great potential in targeted drug delivery due to their inflammatory homing and immune escape capabilities. , Compared with live engineered macrophages or macrophage membranes, inactivated macrophages avoid the risk of exacerbating inflammation and highly preserve the complete cell membrane structures, thereby affording a safe and natural inflammation-targeted agent …”
Section: Introductionmentioning
confidence: 99%
“…Functional components-anchored cell platforms have emerged as versatile tools for targeting a variety of lesions, such as engineered immune cells, stem cells, tumor cells, bacteria, and platelets. Macrophages (Mø) is a type of phagocytes with strong migratory properties to remove foreign debris and cells from an injury site. When the tissue becomes infected or damaged, inflammatory monocytes’ CC chemokines 2 (CCR2) interact with monocyte chemotactic protein (MCP-1), causing mononuclear cells to differentiate into macrophages and migrate to the injured area . Engineered macrophages have shown great potential in targeted drug delivery due to their inflammatory homing and immune escape capabilities. , Compared with live engineered macrophages or macrophage membranes, inactivated macrophages avoid the risk of exacerbating inflammation and highly preserve the complete cell membrane structures, thereby affording a safe and natural inflammation-targeted agent …”
Section: Introductionmentioning
confidence: 99%