Department of Chemistry, University of North Carolina at Chapel Hill (USA); Department of Chemistry and Biology, York University (Canada).
Angew Chem Int Ed Engl. 2014 Sep 1;53(36):9487-92. doi: 10.1002/anie.201404099. Epub 2014 Jul 7.
We report a strategy to rewire cell surfaces for the dynamic control of ligand composition on cell membranes and the modulation of cell-cell interactions to generate three-dimensional (3D) tissue structures applied to stem-cell differentiation, cell-surface tailoring, and tissue engineering. We tailored cell surfaces with bioorthogonal chemical groups on the basis of a liposome-fusion and -delivery method to create dynamic, electroactive, and switchable cell-tissue assemblies through chemistry involving chemoselective conjugation and release. Each step to modify the cell surface: activation, conjugation, release, and regeneration, can be monitored and modulated by noninvasive, label-free analytical techniques. We demonstrate the utility of this methodology by the conjugation and release of small molecules to and from cell surfaces and by the generation of 3D coculture spheroids and multilayered cell tissues that can be programmed to undergo assembly and disassembly on demand.
我们报告了一种用于动态控制细胞膜上配体组成和调节细胞间相互作用的细胞表面重布线策略,以生成应用于干细胞分化、细胞表面修饰和组织工程的三维(3D)组织结构。我们基于脂质体融合和递送来对细胞表面进行了生物正交化学基团的修饰,通过涉及化学选择性缀合和释放的化学方法来创建动态、电活性和可切换的细胞组织组件。修饰细胞表面的每一步:激活、缀合、释放和再生,都可以通过非侵入性、无标记的分析技术进行监测和调节。我们通过小分子与细胞表面的缀合和释放以及 3D 共培养球体和多层细胞组织的生成来证明这种方法的实用性,这些球体和组织可以被编程为按需进行组装和拆卸。
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