High-throughput Peptide epitope mapping using carbon nanotube field-effect transistors.

International Journal of Peptides Pub Date : 2013-01-01 Epub Date: 2013-07-14 DOI:10.1155/2013/849303
Steingrimur Stefansson, Martha Knight, Hena H Kwon, Lára A Stefansson, Saeyoung Nate Ahn
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引用次数: 3

Abstract

Label-free and real-time detection technologies can dramatically reduce the time and cost of pharmaceutical testing and development. However, to reach their full promise, these technologies need to be adaptable to high-throughput automation. To demonstrate the potential of single-walled carbon nanotube field-effect transistors (SWCNT-FETs) for high-throughput peptide-based assays, we have designed circuits arranged in an 8 × 12 (96-well) format that are accessible to standard multichannel pipettors. We performed epitope mapping of two HIV-1 gp160 antibodies using an overlapping gp160 15-mer peptide library coated onto nonfunctionalized SWCNTs. The 15-mer peptides did not require a linker to adhere to the non-functionalized SWCNTs, and binding data was obtained in real time for all 96 circuits. Despite some sequence differences in the HIV strains used to generate these antibodies and the overlapping peptide library, respectively, our results using these antibodies are in good agreement with known data, indicating that peptides immobilized onto SWCNT are accessible and that linear epitope mapping can be performed in minutes using SWCNT-FET.

Abstract Image

Abstract Image

利用碳纳米管场效应晶体管进行高通量肽表位定位。
无标签和实时检测技术可以大大减少药物测试和开发的时间和成本。然而,为了充分发挥其潜力,这些技术需要适应高通量自动化。为了证明单壁碳纳米管场效应晶体管(swcnts - fet)在高通量多肽检测中的潜力,我们设计了8 × 12(96孔)格式的电路,可用于标准的多通道移液器。我们使用覆盖在非功能化SWCNTs上的重叠gp160 15-mer肽文库对两种HIV-1 gp160抗体进行了表位定位。15-mer肽不需要连接物粘附在非功能化SWCNTs上,并且所有96个电路的结合数据都是实时获得的。尽管用于产生这些抗体和重叠肽库的HIV毒株之间存在一些序列差异,但我们使用这些抗体的结果与已知数据非常一致,这表明固定在swcnts上的肽是可获得的,并且使用swcnts - fet可以在几分钟内完成线性表位定位。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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