TY - JOUR
T1 - Growth and site-specific organization of micron-scale biomolecular devices on living mammalian cells
AU - Jia, Sisi
AU - Phua, Siew Cheng
AU - Nihongaki, Yuta
AU - Li, Yizeng
AU - Pacella, Michael
AU - Li, Yi
AU - Mohammed, Abdul M.
AU - Sun, Sean
AU - Inoue, Takanari
AU - Schulman, Rebecca
N1 - Funding Information:
The authors thank Samuel Schaffter, Yi Li and Pepijn Moerman for helpful discussion, Kostas Konstantopoulos, Panagiotis Mistriotis, and Kaustav Bera for technical assistance and HeLa-GFP cell lines, Michael McCaffrey and Erin Prycell for imaging assistance. S.J., Yi Li and R.S. acknowledge support from DARPA BTO Award D16AP00147 (YFA) and NSF CMMI-1562661. This work was supported in part by the US National Institutes of Health (NIH) grant to T.I. (DK102910). S.C.P. was supported by the Agency for Science, Technology and Research (Singapore). Y.N. was supported by postdoctoral fellowships from Japan Society for the Promotion of Science and from the Uehara Memorial Foundation. Yizeng L. and S.S. acknowledge support from NIH R01GM134542.
Publisher Copyright:
© 2021, The Author(s).
PY - 2021/12/1
Y1 - 2021/12/1
N2 - 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/cm2, 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.
AB - 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/cm2, 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.
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U2 - 10.1038/s41467-021-25890-z
DO - 10.1038/s41467-021-25890-z
M3 - Article
C2 - 34593818
AN - SCOPUS:85116341481
SN - 2041-1723
VL - 12
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 5729
ER -