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本文引用的文献

1
Electrostatic melting in a single-molecule field-effect transistor with applications in genomic identification.单分子场效应晶体管中的静电熔化及其在基因组识别中的应用。
Nat Commun. 2017 May 18;8:15450. doi: 10.1038/ncomms15450.
2
Single-Molecule Reaction Chemistry in Patterned Nanowells.在图案化纳米井中的单分子反应化学。
Nano Lett. 2016 Jul 13;16(7):4679-85. doi: 10.1021/acs.nanolett.6b02149. Epub 2016 Jun 7.
3
Quantification of Fewer than Ten Copies of a DNA Biomarker without Amplification or Labeling.定量检测未经扩增或标记的少于十个拷贝的 DNA 生物标志物。
J Am Chem Soc. 2016 Jun 8;138(22):7075-81. doi: 10.1021/jacs.6b02791. Epub 2016 May 26.
4
Complementary Metal-Oxide-Semiconductor Integrated Carbon Nanotube Arrays: Toward Wide-Bandwidth Single-Molecule Sensing Systems.互补金属氧化物半导体集成碳纳米管阵列:迈向宽带宽单分子传感系统
Nano Lett. 2016 Apr 13;16(4):2674-9. doi: 10.1021/acs.nanolett.6b00319. Epub 2016 Mar 24.
5
Structural dynamics of potassium-channel gating revealed by single-molecule FRET.单分子荧光共振能量转移揭示钾通道门控的结构动力学
Nat Struct Mol Biol. 2016 Jan;23(1):31-36. doi: 10.1038/nsmb.3138. Epub 2015 Dec 7.
6
Impact of holdase chaperones Skp and SurA on the folding of β-barrel outer-membrane proteins.持家伴侣 Skp 和 SurA 对β桶型外膜蛋白折叠的影响。
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Data analysis methods for solid-state nanopores.固态纳米孔的数据分析方法。
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9
Defining and overcoming the contact resistance challenge in scaled carbon nanotube transistors.在规模化碳纳米管晶体管中定义和克服接触电阻挑战。
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10
Characterization of organic fluorophores for in vivo FRET studies based on electroporated molecules.基于电穿孔分子的用于体内荧光共振能量转移(FRET)研究的有机荧光团的表征
Phys Chem Chem Phys. 2014 Jul 7;16(25):12688-94. doi: 10.1039/c4cp00995a.

电可控的旋涂碳纳米管场效应晶体管阵列单点共价功能化。

Electrically Controllable Single-Point Covalent Functionalization of Spin-Cast Carbon-Nanotube Field-Effect Transistor Arrays.

机构信息

Department of Electrical Engineering , Columbia University , New York , New York 10027 , United States.

Pacific Biosciences , Menlo Park , California 94025 , United States.

出版信息

ACS Nano. 2018 Oct 23;12(10):9922-9930. doi: 10.1021/acsnano.8b03073. Epub 2018 Oct 3.

DOI:10.1021/acsnano.8b03073
PMID:30260623
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6887518/
Abstract

Single-point-functionalized carbon-nanotube field-effect transistors (CNTFETs) have been used to sense conformational changes and binding events in protein and nucleic acid structures from intrinsic molecular charge. The key to utilizing these devices as single-molecule sensors is the ability to attach a single probe molecule to an individual device. In contrast, with noncovalent attachment approaches such as those based on van der Waals interactions, covalent attachment approaches generally deliver higher stability but have traditionally been more difficult to control, resulting in low yield. Here, we present a single-point-functionalization method for CNTFET arrays based on electrochemical control of a diazonium reaction to create sp defects, combined with a scalable spin-casting method for fabricating large arrays of devices on arbitrary substrates.  Attachment of probe DNA to the functionalized device enables single-molecule detection of DNA hybridization with complementary target, verifying the single-point functionalization. Overall, this method enables single-point defect generation with 80% yield.

摘要

单点功能化的碳纳米管场效应晶体管(CNTFET)已被用于从内在分子电荷中感应蛋白质和核酸结构的构象变化和结合事件。利用这些器件作为单分子传感器的关键是能够将单个探针分子附着到单个器件上。相比之下,基于范德华相互作用的非共价附着方法,共价附着方法通常提供更高的稳定性,但传统上更难控制,导致产量低。在这里,我们提出了一种基于电化学控制的叠氮反应在 CNTFET 阵列上进行单点功能化的方法,该方法产生 sp 缺陷,并结合了一种可扩展的旋涂方法,可在任意基底上制造大型器件阵列。将探针 DNA 附着到功能化的器件上,可实现与互补靶标 DNA 杂交的单分子检测,从而验证单点功能化。总的来说,这种方法可以以 80%的产率产生单点缺陷。