Growth and site-specific organization of micron-scale biomolecular devices on living mammalian cells
Sisi Jia (1), Siew Cheng Phua (2), Yuta Nihongaki (2), Yizeng Li (3, and 5), Michael Pacella (1), Yi Li (1), Abdul M. Mohammed (1), Sean Sun (3),, Takanari Inoue (2), Rebecca Schulman (1, 4) ((1) Chemical, Biomolecular, Engineering, Johns Hopkins University, Baltimore, USA

TL;DR
This paper demonstrates the integration of synthetic micro-scale filaments and DNA nanotubes onto mammalian cell surfaces, enabling shear stress measurement and dynamic cellular components, advancing cell surface engineering and biosensing capabilities.
Contribution
It introduces a method to precisely anchor synthetic biomolecular structures on living cells, maintaining their organization during cellular activity, which was previously challenging.
Findings
Nanotubes act as shear stress sensors, measuring 0-2 dyn/cm².
Anchored nanotubes can grow dynamically on cell surfaces.
The approach enables organized cell surface engineering with synthetic structures.
Abstract
Mesoscale molecular assemblies on the cell surface, such as cilia and filopodia, integrate information, control transport and amplify signals. Synthetic devices mimicking these structures could sensitively monitor these cellular functions and direct new ones. The challenges in creating such devices, however are that they must be integrated with cells in a precise kinetically controlled process and a device's structure and its precisely structured cell interface must then be maintained during active cellular function. Here we report the ability to integrate synthetic micro-scale filaments, DNA nanotubes, into a cell's architecture by anchoring them by their ends to specific receptors on the surfaces of mammalian cells. These filaments can act as shear stress meters: how anchored nanotubes bend at the cell surface quantitatively indicates the magnitude of shear stresses between 0-2 dyn…
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