Department of Mechanical Engineering.
Department of Internal Medicine, Division of Hematology/Oncology, and.
Blood. 2021 Mar 25;137(12):1591-1602. doi: 10.1182/blood.2019004399.
Digital protein assays have great potential to advance immunodiagnostics because of their single-molecule sensitivity, high precision, and robust measurements. However, translating digital protein assays to acute clinical care has been challenging because it requires deployment of these assays with a rapid turnaround. Herein, we present a technology platform for ultrafast digital protein biomarker detection by using single-molecule counting of immune-complex formation events at an early, pre-equilibrium state. This method, which we term "pre-equilibrium digital enzyme-linked immunosorbent assay" (PEdELISA), can quantify a multiplexed panel of protein biomarkers in 10 µL of serum within an unprecedented assay incubation time of 15 to 300 seconds over a 104 dynamic range. PEdELISA allowed us to perform rapid monitoring of protein biomarkers in patients manifesting post-chimeric antigen receptor T-cell therapy cytokine release syndrome, with ∼30-minute sample-to-answer time and a sub-picograms per mL limit of detection. The rapid, sensitive, and low-input volume biomarker quantification enabled by PEdELISA is broadly applicable to timely monitoring of acute disease, potentially enabling more personalized treatment.
数字蛋白分析在免疫诊断学中有很大的应用潜力,因为它们具有单分子灵敏度、高精度和稳健的测量能力。然而,将数字蛋白分析转化为急性临床护理具有挑战性,因为它需要快速周转时间来部署这些分析。在此,我们提出了一种超快数字蛋白生物标志物检测技术平台,该平台利用在早期预平衡状态下免疫复合物形成事件的单分子计数来实现。这种方法,我们称之为“预平衡数字酶联免疫吸附测定(PEdELISA)”,可以在 15 至 300 秒的空前测定孵育时间内,在 10µL 血清中定量分析多达 10 个蛋白生物标志物,动态范围为 104。PEdELISA 允许我们对表现出嵌合抗原受体 T 细胞治疗细胞因子释放综合征的患者进行蛋白生物标志物的快速监测,其样品至答案的时间约为 30 分钟,检测限为亚皮克每毫升。PEdELISA 实现的快速、灵敏和低输入体积的生物标志物定量分析具有广泛的适用性,可用于及时监测急性疾病,从而有可能实现更个性化的治疗。