Department of Chemistry , University of Calgary , Calgary , Alberta T2N 1N4 , Canada.
Department of Chemistry , Clemson University , Clemson , South Carolina 29634 , United States.
ACS Sens. 2019 Jan 25;4(1):143-151. doi: 10.1021/acssensors.8b01069. Epub 2018 Dec 31.
A major challenge in effectively treating infections is to provide timely diagnosis of a bacterial or viral agent. Current cell culture methods require >24 h to identify the cause of infection. The Toll-like Receptor (TLR) family of proteins can identify classes of pathogens and has been shown to work well in an impedance-based biosensor, where the protein is attached to an electrode via a self-assembled monolayer (SAM). While the sensitivity of these sensors has been good, they contain a high resistance (>1 kΩ) SAM, generating relatively small signals and requiring longer data collection, which is ill-suited to implementation outside of a laboratory. Here, we describe a novel approach to increase the signal magnitude and decrease the measurement time of a TLR-4 biosensor by inserting a redox-active ferrocenyl-terminated alkanethiol into a mixed SAM containing hydroxyl- and carboxyl-terminated alkanethiols. The SAM formation and modification was confirmed via contact angle and X-ray photoelectron spectroscopy measurements, with TLR-4 immobilization demonstrated through a modified immunosorbent assay. It is shown that these TLR-4 biosensors respond selectively to their intended target, Gram-negative bacteria at levels between 1 and 10 lysed cells/mL, while remaining insensitive to Gram-positive bacteria or viral particles at up to 10 particles/mL. Furthermore, the signal enhancement due to the addition of ferrocene decreased the measurement time to less than 1 min and has enabled this sensor to be used with an inexpensive, portable, hand-held potentiostat that could be easily implemented in field settings.
有效治疗感染的一个主要挑战是及时诊断细菌或病毒病原体。目前的细胞培养方法需要超过 24 小时才能确定感染的原因。Toll 样受体(TLR)蛋白家族可以识别病原体类别,并已在基于阻抗的生物传感器中得到很好的应用,其中蛋白质通过自组装单层(SAM)附着在电极上。虽然这些传感器的灵敏度很好,但它们包含高电阻(>1 kΩ)SAM,产生相对较小的信号,需要更长的数据采集时间,这不利于在实验室之外实施。在这里,我们描述了一种通过将氧化还原活性的二茂铁端烷硫醇插入含有羟基和羧基端烷硫醇的混合 SAM 来增加 TLR-4 生物传感器信号幅度并缩短测量时间的新方法。通过接触角和 X 射线光电子能谱测量来确认 SAM 的形成和修饰,通过改良的免疫吸附测定来证明 TLR-4 的固定化。结果表明,这些 TLR-4 生物传感器可以选择性地响应其预期目标,革兰氏阴性菌的浓度范围为 1 至 10 个裂解细胞/mL,而对革兰氏阳性菌或病毒颗粒的敏感性保持在 10 个颗粒/mL 以下。此外,由于添加二茂铁而增强的信号降低了测量时间不到 1 分钟,并使该传感器能够与廉价、便携式、手持式电化学工作站一起使用,该工作站可以很容易地在现场环境中实施。