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利用碳纳米管进行微注射时对细胞穿透的电检测。

Electrical detection of cellular penetration during microinjection with carbon nanopipettes.

机构信息

University of Pennsylvania, Department of Mechanical Engineering and Applied Mechanics, Towne Bldg. 229, 220 S. 33rd St., Philadelphia, PA 19104, USA.

出版信息

Nanotechnology. 2014 Jun 20;25(24):245102. doi: 10.1088/0957-4484/25/24/245102. Epub 2014 May 23.

Abstract

The carbon nanopipette (CNP) is comprised of a pulled-glass pipette terminating with a nanoscale (tens to hundreds of nm) diameter carbon pipe. The entire inner glass surface of the CNP is coated with a carbon film, providing an electrically conductive path from the carbon tip to the distal, macroscopic end of the pipette. The CNP can double as a nanoelectrode, enabling electrical measurements through its carbon lining, and as a nanoinjector, facilitating reagent injection through its hollow bore. With the aid of a lock-in amplifier, we measured, in real time and with millisecond resolution, variations in impedance and interfacial capacitance as the CNP penetrated into the cytoplasm and nucleus of adherent human osteosarcoma (U20S) cells during microinjection. The capacitance change associated with nucleus penetration was, on average, 1.5 times greater than the one associated with cell membrane penetration. The experimental data was compared and favorably agreed with theoretical predictions based on a simple electrical network model. As a proof of concept, the cytoplasm and nucleus were transfected with fluorescent tRNA, enabling real-time monitoring of tRNA trafficking across the nuclear membrane. The CNP provides a robust and reliable means to detect cell and nucleus penetration, and trigger injection, thereby enabling the automation of cell injection.

摘要

碳纳米管(CNP)由拉制的玻璃管末端的纳米级(数十至数百纳米)直径碳管组成。CNP 的整个内玻璃表面都涂有一层碳膜,为从碳尖端到玻璃管远端的宏观端提供了一个导电路径。CNP 可以兼作纳米电极,通过其碳衬里进行电测量,也可以作为纳米注射器,通过其空心管进行试剂注射。在锁相放大器的帮助下,我们实时测量了 CNP 在微注射过程中穿透贴壁人骨肉瘤(U20S)细胞的细胞质和细胞核时阻抗和界面电容的变化,分辨率为毫秒级。与细胞膜穿透相关的电容变化平均比与核穿透相关的电容变化大 1.5 倍。实验数据与基于简单电网络模型的理论预测进行了比较,并得到了很好的一致。作为概念验证,细胞质和细胞核被荧光 tRNA 转染,从而能够实时监测 tRNA 穿过核膜的运输。CNP 提供了一种强大可靠的方法来检测细胞和细胞核的穿透,并触发注射,从而实现细胞注射的自动化。

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