Laboratory of Biosensors and Bioinstruments, National Laboratory Astana, Nazarbayev University, 010000 Astana, Kazakhstan.
Department of Biology, School of Sciences and Humanities, Nazarbayev University, 010000 Astana, Kazakhstan.
Sensors (Basel). 2024 Mar 21;24(6):1991. doi: 10.3390/s24061991.
The accuracy and efficacy of medical treatment would be greatly improved by the continuous and real-time monitoring of protein biomarkers. Identification of cancer biomarkers in patients with solid malignant tumors is receiving increasing attention. Existing techniques for detecting cancer proteins, such as the enzyme-linked immunosorbent assay, require a lot of work, are not multiplexed, and only allow for single-time point observations. In order to get one step closer to clinical usage, a dynamic platform for biosensing the cancer biomarker CD44 using a single-mode optical fiber-based ball resonator biosensor was designed, constructed and evaluated in this work. The main novelty of the work is an in-depth study of the capability of an in-house fabricated optical fiber biosensor for in situ detection of a cancer biomarker (CD44 protein) by conducting several types of experiments. The main results of the work are as follows: (1) Calibration of the fabricated fiber-optic ball resonator sensors in both static and dynamic conditions showed similar sensitivity to the refractive index change demonstrating its usefulness as a biosensing platform for dynamic measurements; (2) The fabricated sensors were shown to be insensitive to pressure changes further confirming their utility as an in situ sensor; (3) The sensor's packaging and placement were optimized to create a better environment for the fabricated ball resonator's performance in blood-mimicking environment; (4) Incubating increasing protein concentrations with antibody-functionalized sensor resulted in nearly instantaneous signal change indicating a femtomolar detection limit in a dynamic range from 7.1 aM to 16.7 nM; (5) The consistency of the obtained signal change was confirmed by repeatability studies; (6) Specificity experiments conducted under dynamic conditions demonstrated that the biosensors are highly selective to the targeted protein; (7) Surface morphology studies by AFM measurements further confirm the biosensor's exceptional sensitivity by revealing a considerable shift in height but no change in surface roughness after detection. The biosensor's ability to analyze clinically relevant proteins in real time with high sensitivity offers an advancement in the detection and monitoring of malignant tumors, hence improving patient diagnosis and health status surveillance.
通过对蛋白质生物标志物的连续实时监测,可以极大地提高医疗的准确性和疗效。在实体恶性肿瘤患者中鉴定癌症生物标志物受到越来越多的关注。现有的癌症蛋白检测技术,如酶联免疫吸附测定法,需要大量的工作,不能进行多重检测,并且只能进行单次检测。为了更接近临床应用,本工作设计、构建和评估了一种使用基于单模光纤的球谐振器生物传感器对癌症生物标志物 CD44 进行生物传感的动态平台。本工作的主要新颖之处在于通过进行多种类型的实验,深入研究了自制光纤生物传感器对原位检测癌症生物标志物(CD44 蛋白)的能力。本工作的主要结果如下:(1)在静态和动态条件下对所制备的光纤球谐振器传感器进行校准,结果表明其对折射率变化的灵敏度相似,证明其作为用于动态测量的生物传感平台的有用性;(2)所制备的传感器对压力变化不敏感,进一步证实了其作为原位传感器的实用性;(3)对传感器的封装和放置进行了优化,以在类似血液的环境中为所制备的球谐振器的性能创造更好的环境;(4)用抗体功能化的传感器孵育浓度不断增加的蛋白质,导致信号几乎瞬间发生变化,表明在 7.1 aM 至 16.7 nM 的动态范围内具有飞摩尔检测限;(5)通过重复性研究证实了获得的信号变化的一致性;(6)在动态条件下进行的特异性实验表明,生物传感器对目标蛋白具有高度选择性;(7)原子力显微镜测量的表面形貌研究进一步通过显示在检测后高度有相当大的位移但表面粗糙度没有变化来证实生物传感器的超高灵敏度。该生物传感器具有实时高灵敏度分析临床相关蛋白的能力,为恶性肿瘤的检测和监测提供了新的方法,从而改善了患者的诊断和健康状况监测。