Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA.
Anal Chem. 2011 Dec 1;83(23):9138-45. doi: 10.1021/ac202335u. Epub 2011 Nov 7.
Highly sensitive and multiplexed detection of clinically relevant proteins in biologically complex samples is crucial for the advancement of clinical proteomics. In recent years, aptamers have emerged as useful tools for protein analysis due to their specificity and affinity for protein targets as well as their compatibility with particle-based detection systems. In this study, we demonstrate the highly sensitive detection of human α-thrombin on encoded hydrogel microparticles functionalized with an aptamer capture sequence. We use static imaging and microfluidic flow-through analysis techniques to evaluate the detection capabilities of the microgels in sandwich-assay formats that utilize both aptamers and antibodies for the reporting of target-binding events. Buffers and reagent concentrations were optimized to provide maximum reaction efficiency while still maintaining an assay with a simple workflow that can be easily adapted to the multiplexed detection of other clinically relevant proteins. The three-dimensional, nonfouling hydrogel immobilization scaffold used in this work provides three logs of dynamic range, with a limit of detection of 4 pM using a single aptamer capture species and without the need for spacers or signal amplification.
在生物复杂样本中对临床相关蛋白质进行高灵敏度和多重检测对于临床蛋白质组学的发展至关重要。近年来,由于适配体对蛋白质靶标具有特异性和亲和力,以及与基于粒子的检测系统兼容,因此它们已成为蛋白质分析的有用工具。在这项研究中,我们展示了在经适配体捕获序列功能化的编码水凝胶微珠上对人凝血酶α的高灵敏度检测。我们使用静态成像和微流控流动分析技术,评估了微珠在三明治分析格式中的检测能力,该格式利用适配体和抗体报告靶结合事件。优化了缓冲液和试剂浓度,以提供最大的反应效率,同时仍然保持具有简单工作流程的测定,该流程可轻松适应其他临床相关蛋白质的多重检测。在这项工作中使用的三维、非缠结水凝胶固定化支架提供了三个数量级的动态范围,使用单个适配体捕获物种的检测限为 4 pM,而无需间隔物或信号放大。