Department of Material Science and Engineering, University of California, Santa Barbara, CA 93106, USA.
Analyst. 2019 Aug 16;144(17):5277-5283. doi: 10.1039/c9an00455f.
The faster a disease can be diagnosed, the sooner effective treatment can be initiated, motivating a drive to replace standard laboratory techniques with point-of-care technologies that return answers in minutes rather than hours. Thus motivated, we describe the development of an E-DNA scaffold sensor for the rapid and convenient measurement of antibodies diagnostic of syphilis. To achieve this (and in contrast to previous sensors of this class, which relied on single, linear epitopes for detection), we utilized a near full-length antigen as the sensor's recognition element, allowing us to simultaneously display multiple epitopes. The resultant sensor is able to detect antibodies against Treponema pallidum pallidum, the causative agent of syphilis, at clinically relevant concentrations in samples in less than 10 min. Preliminary results obtained using sero-positive and sero-negative human samples suggest the clinical sensitivity and specificity of the approach compare well to current gold-standard tests, while being simple and rapid enough to deploy at the point of care.
疾病诊断得越快,就能越早开始有效治疗,这促使人们努力用即时检测技术替代标准实验室技术,从而将答案从数小时缩短至数分钟。受此启发,我们描述了一种 E-DNA 支架传感器的开发,用于快速便捷地测量诊断梅毒的抗体。为了实现这一目标(与之前依赖单个线性表位进行检测的此类传感器相反),我们使用近乎全长的抗原作为传感器的识别元件,从而能够同时显示多个表位。该传感器能够在不到 10 分钟的时间内,以临床相关浓度检测到针对梅毒螺旋体的抗体,这是梅毒的病原体。使用血清阳性和血清阴性的人类样本获得的初步结果表明,该方法的临床灵敏度和特异性与当前的金标准检测相当,同时足够简单快速,可以在即时检测点使用。