Yang J, Zhu J, Pei R, Oliver J A, Landry D W, Stojanovic M N, Lin Q
Department of Mechanical Engineering, Columbia University, New York, NY 10027, United States.
Suzhou Institute of Nano-Tech and Nano-Bionics, Chinese Academy of Sciences, Suzhou, China.
Anal Methods. 2016 Jul 14;8(26):5190-5196. doi: 10.1039/C5AY02979A. Epub 2016 May 11.
We present a microfluidic aptamer-based biosensor for detection of low-molecular-weight biomarkers in patient samples. Using a microfluidic device that integrates aptamer-based specific analyte extraction, isocratic elution, and detection by matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) mass spectrometry, we demonstrate rapid, sensitive and label-free detection of arginine vasopressin (AVP) in human plasma ultrafiltrate. AVP molecules in complex matrices are specifically captured by an aptamer that is immobilized on microbeads via affinity binding in a microchamber. After the removal of unbound, contaminating molecules through washing, aptamer-AVP complexes are thermally disrupted via on-chip temperature control. Released AVP molecules are eluted with purified water and transferred to a separate microchamber, and deposited onto a single spot on a MALDI plate via repeated, piezoelectrically actuated ejection, which enriches AVP molecules over the spot area. This integrated on-chip sample processing enables the quantitative detection of low-abundance AVP by MALDI-TOF mass spectrometry in a rapid and label-free manner. Our experimental results show the detection of AVP in human plasma ultrafiltrate as low as physiologically relevant picomolar concentrations via aptamer-based selective preconcentration, demonstrating the potential of our approach as a rapid (~ 1hr), sensitive clinical AVP assay.
我们展示了一种基于微流控适配体的生物传感器,用于检测患者样本中的低分子量生物标志物。通过使用一种微流控装置,该装置集成了基于适配体的特定分析物提取、等度洗脱以及通过基质辅助激光解吸/电离飞行时间(MALDI-TOF)质谱进行检测,我们证明了能够对人血浆超滤液中的精氨酸加压素(AVP)进行快速、灵敏且无标记的检测。复杂基质中的AVP分子通过在微腔室中通过亲和结合固定在微珠上的适配体特异性捕获。在通过洗涤去除未结合的污染分子后,通过芯片上的温度控制使适配体-AVP复合物热解聚。释放的AVP分子用纯水洗脱并转移到单独的微腔室中,并通过重复的压电驱动喷射沉积到MALDI板上的单个斑点上,这在斑点区域富集了AVP分子。这种集成的芯片上样品处理能够通过MALDI-TOF质谱以快速且无标记的方式对低丰度AVP进行定量检测。我们的实验结果表明,通过基于适配体的选择性预浓缩,能够检测出人血浆超滤液中低至生理相关皮摩尔浓度的AVP,证明了我们的方法作为一种快速(约1小时)、灵敏的临床AVP检测方法的潜力。