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利用纳米等离子体-光子混合微腔实现对单个蛋白质的无标记检测。

Label-free detection of single protein using a nanoplasmonic-photonic hybrid microcavity.

机构信息

Microparticle Photophysics Lab, Polytechnic Institute of NYU , Brooklyn, New York 11201, United States.

出版信息

Nano Lett. 2013 Jul 10;13(7):3347-51. doi: 10.1021/nl401633y. Epub 2013 Jun 20.

Abstract

Recently we reported the detection and sizing of the smallest RNA virus MS2 with a mass of 6 ag from the resonance frequency shift of a whispering gallery mode-nanoshell hybrid resonator (WGM-h) upon adsorption on the nanoshell and anticipated that single protein above 0.4 ag should be detectable but with considerably smaller signals. Here, we report the detection of single thyroid cancer marker (Thyroglobulin, Tg) and bovine serum albumin (BSA) proteins with masses of only 1 ag and 0.11 ag (66 kDa), respectively. However, the wavelength shifts are enhanced beyond those anticipated in our earlier work by 240% for Tg and 1500% for BSA. This surprising sensitivity is traced to a short-range reactive field near the surface of our Au nanoshell receptor due to intrinsic random bumps of protein size, leading to an unanticipated increase in sensitivity to single protein, which grows larger as the protein diminishes in size. As a consequence of the largest signal-to-noise ratio in our BSA experiments (S/N ≈ 13), we conservatively estimated a new protein limit of detection for our WGM-h of 5 kDa.

摘要

最近,我们报道了通过 whispering gallery mode-nanoshell 混合谐振器(WGM-h)的共振频率移动来检测和测量最小 RNA 病毒 MS2 的大小,其质量为 6 ag,当病毒吸附在纳米壳上时,我们预计质量超过 0.4 ag 的单个蛋白应该是可检测的,但信号要小得多。在这里,我们报告了对单个甲状腺癌标志物(甲状腺球蛋白,Tg)和牛血清白蛋白(BSA)蛋白的检测,它们的质量分别仅为 1 ag 和 0.11 ag(66 kDa)。然而,与我们早期工作中的预期相比,Tg 的波长移动增强了 240%,BSA 的波长移动增强了 1500%。这种令人惊讶的灵敏度可归因于我们的 Au 纳米壳受体表面附近的短程反应场,由于蛋白质尺寸的固有随机波动,导致对单个蛋白质的灵敏度出乎意料地增加,随着蛋白质尺寸的减小而增大。由于我们在 BSA 实验中具有最大的信噪比(S/N ≈ 13),我们保守地估计我们的 WGM-h 的新蛋白质检测极限为 5 kDa。

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