Author: García-López V1,2, Chen F3, Nilewski LG1,2, Duret G4, Aliyan A1, Kolomeisky AB1, Robinson JT4, Wang G3, Pal R5, Tour JM1,2,6
Affiliation:
1Department of Chemistry, Rice University, Houston, Texas 77005, USA.
2Smalley-Curl Institute and NanoCarbon Center, Rice University, Houston, Texas 77005, USA.
3Department of Chemistry, North Carolina State University, Raleigh, North Carolina 27695, USA.
4Department of Electrical and Computer Engineering, Rice University, Houston, Texas 77005, USA.
5Department of Chemistry, Durham University, South Road, Durham DH1 3LE, UK.
6Department of Materials Science and NanoEngineering, Rice University, Houston, Texas 77005, USA.
Conference/Journal: Nature.
Date published: 2017 Aug 30
Other:
Volume ID: 548 , Issue ID: 7669 , Pages: 567-572 , Special Notes: doi: 10.1038/nature23657. , Word Count: 233
Beyond the more common chemical delivery strategies, several physical techniques are used to open the lipid bilayers of cellular membranes. These include using electric and magnetic fields, temperature, ultrasound or light to introduce compounds into cells, to release molecular species from cells or to selectively induce programmed cell death (apoptosis) or uncontrolled cell death (necrosis). More recently, molecular motors and switches that can change their conformation in a controlled manner in response to external stimuli have been used to produce mechanical actions on tissue for biomedical applications. Here we show that molecular machines can drill through cellular bilayers using their molecular-scale actuation, specifically nanomechanical action. Upon physical adsorption of the molecular motors onto lipid bilayers and subsequent activation of the motors using ultraviolet light, holes are drilled in the cell membranes. We designed molecular motors and complementary experimental protocols that use nanomechanical action to induce the diffusion of chemical species out of synthetic vesicles, to enhance the diffusion of traceable molecular machines into and within live cells, to induce necrosis and to introduce chemical species into live cells. We also show that, by using molecular machines that bear short peptide addends, nanomechanical action can selectively target specific cell-surface recognition sites. Beyond the in vitro applications demonstrated here, we expect that molecular machines could also be used in vivo, especially as their design progresses to allow two-photon, near-infrared and radio-frequency activation.
PMID: 28858304 DOI: 10.1038/nature23657