Department of Chemistry, Institute for Genomic Biology, and Micro and Nanotechnology Laboratory, University of Illinois at Urbana-Champaign, 600 South Mathews Avenue, Urbana, Illinois 61801, USA.
Anal Chem. 2010 Mar 1;82(5):1975-81. doi: 10.1021/ac902725q.
The ability to perform multiple simultaneous protein biomarker measurements in complex media with picomolar sensitivity presents a large challenge to disease diagnostics and fundamental biological studies. Silicon photonic microring resonators represent a promising platform for real-time detection of biomolecules on account of their spectral sensitivity toward surface binding events between a target and antibody-modified microrings. For all refractive index-based sensing schemes, the mass of bound analytes, in combination with other factors such as antibody affinity and surface density, contributes to the observed signal and measurement sensitivity. Therefore, proteins that are simultaneously low in abundance and have a lower molecular weight are often challenging to detect. By employing a more massive secondary antibody to amplify the signal arising from the initial binding event, it is possible to improve both the sensitivity and the specificity of protein assays, allowing for quantitative sensing in complex sample matrices. Herein, a sandwich assay is used to detect the 15.5 kDa human cytokine interleukin-2 (IL-2) at concentrations down to 100 pg/mL (6.5 pM) and to quantitate unknown solution concentrations over a dynamic range spanning 2.5 orders of magnitude. This same sandwich assay is then used to monitor the temporal secretion profile of IL-2 from Jurkat T lymphocytes in serum-containing cell culture media in the presence of the entire Jurkat secretome. The same temporal secretion analysis is performed in parallel using a commercial ELISA, revealing similar IL-2 concentration profiles but superior precision for the microring resonator sensing platform. Furthermore, we demonstrate the generality of the sandwich assay methodology on the microring resonator platform for the analysis of any biomolecular target for which two high-affinity antibodies exist by detecting the approximately 8 kDa cytokine interleukin-8 (IL-8) with a limit of detection and dynamic range similar to that of IL-2. This work demonstrates the first application of silicon photonic microring resonators for detecting cellular secretion of cytokines and represents an important advance for the detection of protein biomarkers on an emerging analytical platform.
在复杂介质中以皮摩尔灵敏度同时进行多种蛋白质生物标志物测量的能力对疾病诊断和基础生物学研究提出了巨大挑战。硅光子微环谐振器由于其对目标与抗体修饰的微环之间表面结合事件的光谱敏感性,代表了实时检测生物分子的有前途的平台。对于所有基于折射率的传感方案,结合其他因素,如抗体亲和力和表面密度,与结合分析物的质量共同导致观察到的信号和测量灵敏度。因此,同时丰度低且分子量低的蛋白质通常难以检测。通过采用更大量的二级抗体来放大初始结合事件产生的信号,可以提高蛋白质分析的灵敏度和特异性,从而实现复杂样品基质中的定量传感。在此,夹心测定法用于检测浓度低至 100 pg/mL(6.5 pM)的 15.5 kDa 人细胞因子白细胞介素 2(IL-2),并在跨越 2.5 个数量级的动态范围内定量未知溶液浓度。然后,相同的夹心测定法用于监测在含有血清的细胞培养介质中存在整个 Jurkat 分泌组的情况下 Jurkat T 淋巴细胞中 IL-2 的时间分泌谱。使用商业 ELISA 同时进行相同的时间分泌分析,显示出类似的 IL-2 浓度谱,但对于微环谐振器传感平台具有更高的精度。此外,我们通过检测约 8 kDa 的细胞因子白细胞介素 8(IL-8),在微环谐振器平台上展示了夹心测定法方法的通用性,对于存在两种高亲和力抗体的任何生物分子靶标均可进行分析,检测限和动态范围与 IL-2 相似。这项工作展示了硅光子微环谐振器在检测细胞因子分泌方面的首次应用,代表了在新兴分析平台上检测蛋白质生物标志物的重要进展。