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亚 10 纳米级的细胞内生物电子探针,来自纳米线-纳米管异质结构。

Sub-10-nm intracellular bioelectronic probes from nanowire-nanotube heterostructures.

机构信息

Department of Chemistry and Chemical Biology, Harvard University, Cambridge, MA 02138.

出版信息

Proc Natl Acad Sci U S A. 2014 Jan 28;111(4):1259-64. doi: 10.1073/pnas.1323389111. Epub 2014 Jan 13.

Abstract

The miniaturization of bioelectronic intracellular probes with a wide dynamic frequency range can open up opportunities to study biological structures inaccessible by existing methods in a minimally invasive manner. Here, we report the design, fabrication, and demonstration of intracellular bioelectronic devices with probe sizes less than 10 nm. The devices are based on a nanowire-nanotube heterostructure in which a nanowire field-effect transistor detector is synthetically integrated with a nanotube cellular probe. Sub-10-nm nanotube probes were realized by a two-step selective etching approach that reduces the diameter of the nanotube free-end while maintaining a larger diameter at the nanowire detector necessary for mechanical strength and electrical sensitivity. Quasi-static water-gate measurements demonstrated selective device response to solution inside the nanotube, and pulsed measurements together with numerical simulations confirmed the capability to record fast electrophysiological signals. Systematic studies of the probe bandwidth in different ionic concentration solutions revealed the underlying mechanism governing the time response. In addition, the bandwidth effect of phospholipid coatings, which are important for intracellular recording, was investigated and modeled. The robustness of these sub-10-nm bioelectronics probes for intracellular interrogation was verified by optical imaging and recording the transmembrane resting potential of HL-1 cells. These ultrasmall bioelectronic probes enable direct detection of cellular electrical activity with highest spatial resolution achieved to date, and with further integration into larger chip arrays could provide a unique platform for ultra-high-resolution mapping of activity in neural networks and other systems.

摘要

具有宽动态频率范围的生物电子细胞内探头的小型化可以为研究现有方法无法触及的生物结构提供机会,以微创的方式进行。在这里,我们报告了具有小于 10nm 探头尺寸的细胞内生物电子器件的设计、制造和演示。这些器件基于纳米线-纳米管异质结构,其中纳米线场效应晶体管探测器与纳米管细胞探针综合集成。通过两步选择性刻蚀方法实现了小于 10nm 的纳米管探针,该方法在保持纳米线探测器必要的机械强度和电灵敏度的较大直径的同时,减小了纳米管自由端的直径。准静态水门测量证明了器件对纳米管内溶液的选择性响应,而脉冲测量和数值模拟证实了记录快速电生理信号的能力。在不同离子浓度溶液中对探头带宽的系统研究揭示了控制时间响应的基本机制。此外,还研究和建模了对细胞内记录很重要的磷脂涂层的带宽效应。通过光学成像和记录 HL-1 细胞的跨膜静息电位,验证了这些用于细胞内询问的小于 10nm 生物电子探头的稳健性。这些超小型生物电子探头能够以迄今为止达到的最高空间分辨率直接检测细胞电活动,并且通过进一步集成到更大的芯片阵列中,可以为神经网络和其他系统中活动的超高分辨率映射提供独特的平台。

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