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使用基于红外表面等离子体的单级光学生物传感平台,在溶液相中对阿托摩尔浓度进行实时动力学结合研究。

Real-time kinetic binding studies at attomolar concentrations in solution phase using a single-stage opto-biosensing platform based upon infrared surface plasmons.

作者信息

Allsop T, Mou C, Neal R, Mariani S, Nagel D, Tombelli S, Poole A, Kalli K, Hine A, Webb D J, Culverhouse P, Mascini M, Minunni M, Bennion I

出版信息

Opt Express. 2017 Jan 9;25(1):39-58. doi: 10.1364/OE.25.000039.

Abstract

Here we present a new generic opto-bio-sensing platform combining immobilised aptamers on an infrared plasmonic sensing device generated by nano-structured thin film that demonstrates amongst the highest index spectral sensitivities of any optical fibre sensor yielding on average 3.4 × 10 nm/RIU in the aqueous index regime (with a figure of merit of 330) This offers a single stage, solution phase, atto-molar detection capability, whilst delivering real-time data for kinetic studies in water-based chemistry. The sensing platform is based upon optical fibre and has the potential to be multiplexed and used in remote sensing applications. As an example of the highly versatile capabilities of aptamer based detection using our platform, purified thrombin is detected down to 50 attomolar concentration using a volume of 1mm of solution without the use of any form of enhancement technique. Moreover, the device can detect nanomolar levels of thrombin in a flow cell, in the presence of 4.5% w/v albumin solution. These results are important, covering all concentrations in the human thrombin generation curve, including the problematic initial phase. Finally, selectivity is confirmed using complementary and non-complementary DNA sequences that yield performances similar to those obtained with thrombin.

摘要

在此,我们展示了一种新型通用光学生物传感平台,该平台将固定化适体与由纳米结构薄膜产生的红外等离子体传感装置相结合,在水性折射率范围内,其平均折射率光谱灵敏度达到3.4×10 nm/RIU(品质因数为330),是所有光纤传感器中最高的之一。这提供了单步、溶液相、阿托摩尔检测能力,同时为水基化学动力学研究提供实时数据。该传感平台基于光纤,具有多路复用和用于遥感应用的潜力。作为使用我们平台基于适体检测的高度通用能力的一个例子,在不使用任何形式增强技术的情况下,使用1mm体积的溶液可检测到低至50阿托摩尔浓度的纯化凝血酶。此外,该装置能够在流动池中,在存在4.5% w/v白蛋白溶液的情况下检测纳摩尔水平的凝血酶。这些结果很重要,涵盖了人凝血酶生成曲线中的所有浓度,包括有问题的初始阶段。最后,使用互补和非互补DNA序列确认了选择性,其性能与用凝血酶获得的性能相似。

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