Molecular machines open cell membranes

被引:265
作者
Garcia-Lopez, Victor [1 ,2 ]
Chen, Fang [3 ]
Nilewski, Lizanne G. [1 ,2 ]
Duret, Guillaume [4 ]
Aliyan, Amir [1 ]
Kolomeisky, Anatoly B. [1 ]
Robinson, Jacob T. [4 ]
Wang, Gufeng [3 ]
Pal, Robert [5 ]
Tour, James M. [1 ,2 ,6 ]
机构
[1] Rice Univ, Dept Chem, POB 1892, Houston, TX 77005 USA
[2] Rice Univ, Smalley Curl Inst & NanoCarbon Ctr, Houston, TX 77005 USA
[3] North Carolina State Univ, Dept Chem, Raleigh, NC 27695 USA
[4] Rice Univ, Dept Elect & Comp Engn, Houston, TX 77005 USA
[5] Univ Durham, Dept Chem, South Rd, Durham DH1 3LE, England
[6] Rice Univ, Dept Mat Sci & NanoEngn, Houston, TX 77005 USA
基金
美国国家科学基金会; 英国工程与自然科学研究理事会;
关键词
PROSTATE-CANCER; OPTICAL CONTROL; IDENTIFICATION; APOPTOSIS; PORATION; DYNAMICS; VESICLES; BILAYERS; RUPTURE; FUSION;
D O I
10.1038/nature23657
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Beyond the more common chemical delivery strategies, several physical techniques are used to open the lipid bilayers of cellular membranes(1). These include using electric(2) and magnetic(3) fields, temperature(4), ultrasound(5) or light(6) 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(7-9). 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(10).
引用
收藏
页码:567 / 572
页数:6
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