Department of Chemical and Biomolecular Engineering, Johns Hopkins University, Baltimore, MD, 21218, USA.
Department of Cell Biology, Johns Hopkins University School of Medicine, Baltimore, MD, 21205, USA.
Nat Commun. 2021 Sep 30;12(1):5729. doi: 10.1038/s41467-021-25890-z.
Mesoscale molecular assemblies on the cell surface, such as cilia and filopodia, integrate information, control transport and amplify signals. Designer cell-surface assemblies could control these cellular functions. Such assemblies could be constructed from synthetic components ex vivo, making it possible to form such structures using modern nanoscale self-assembly and fabrication techniques, and then oriented on the cell surface. Here we integrate synthetic devices, micron-scale DNA nanotubes, with mammalian cells by anchoring them by their ends to specific cell surface receptors. These filaments can measure shear stresses between 0-2 dyn/cm, a regime important for cell signaling. Nanotubes can also grow while anchored to cells, thus acting as dynamic cell components. This approach to cell surface engineering, in which synthetic biomolecular assemblies are organized with existing cellular architecture, could make it possible to build new types of sensors, machines and scaffolds that can interface with, control and measure properties of cells.
细胞表面的介观分子组装体,如纤毛和丝状伪足,整合信息、控制运输并放大信号。设计的细胞表面组装体可以控制这些细胞功能。这些组装体可以通过体外的合成组件构建,从而使用现代纳米级自组装和制造技术形成这些结构,并在细胞表面进行定向。在这里,我们通过将它们的末端锚定到特定的细胞表面受体,将合成器件、微米级 DNA 纳米管与哺乳动物细胞集成在一起。这些纤维可以测量 0-2 dyn/cm 之间的剪切力,这是细胞信号传导的重要范围。纳米管在固定到细胞上时也可以生长,从而充当动态细胞成分。这种细胞表面工程的方法,其中合成生物分子组装体与现有细胞结构组织在一起,可能使构建新型传感器、机器和支架成为可能,这些传感器、机器和支架可以与细胞相互作用、控制和测量其特性。