Multiscale Origami Structures as Interface for Cells

被引:86
作者
Angelin, Alessandro [1 ]
Weigel, Simone [1 ]
Garrecht, Ruben [1 ]
Meyer, Rebecca [1 ]
Bauer, Jens [1 ]
Kumar, Ravi Kapoor [2 ,3 ]
Hirtz, Michael [2 ,3 ]
Niemeyer, Christof M. [1 ]
机构
[1] Karlsruhe Inst Technol, Inst Biol Interfaces IBG 1, D-76344 Eggenstein Leopoldshafen, Germany
[2] Karlsruhe Inst Technol, Inst Nanotechnol, D-76344 Eggenstein Leopoldshafen, Germany
[3] Karlsruhe Inst Technol, Karlsruhe Nano Micro Facil, D-76344 Eggenstein Leopoldshafen, Germany
关键词
cell cultures; DNA; nanostructures; proteins; surface chemistry; DNA-DIRECTED IMMOBILIZATION; MICROARRAY TECHNOLOGIES; GOLD NANOPARTICLES; PATTERNED SURFACES; PROTEIN BIOCHIPS; SPATIAL CONTROL; LIVING CELLS; FOLDING DNA; NANOSTRUCTURES; MEMBRANE;
D O I
10.1002/anie.201509772
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
A DNA-based platform was developed to address fundamental aspects of early stages of cell signaling in living cells. By site-directed sorting of differently encoded, protein-decorated DNA origami structures on DNA microarrays, we combine the advantages of the bottom-up self-assembly of protein-DNA nanostructures and top-down micropatterning of solid surfaces to create multiscale origami structures as interface for cells (MOSAIC). In a proof-of-principle, we use this technology to analyze the activation of epidermal growth factor (EGF) receptors in living MCF7 cells using DNA origami structures decorated on their surface with distinctive nanoscale arrangements of EGF ligand entities. MOSAIC holds the potential to present to adhered cells well-defined arrangements of ligands with full control over their number, stoichiometry, and precise nanoscale orientation. It therefore promises novel applications in the life sciences, which cannot be tackled by conventional technologies.
引用
收藏
页码:15813 / 15817
页数:5
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