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基于分子印迹的表面等离子体共振生物传感器的快速灵敏检测人血清中α溶血素的研究

Development of a Molecular Imprinting-Based Surface Plasmon Resonance Biosensor for Rapid and Sensitive Detection of Alpha Hemolysin From Human Serum.

机构信息

Division of Infection Medicine, Department of Clinical Sciences Lund, Lund University, Lund, Sweden.

Department of Infection Medicine, Skåne University Hospital, Lund, Sweden.

出版信息

Front Cell Infect Microbiol. 2020 Nov 20;10:571578. doi: 10.3389/fcimb.2020.571578. eCollection 2020.

DOI:10.3389/fcimb.2020.571578
PMID:33330120
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7715021/
Abstract

is a common infectious agent in sepsis, associated with both high mortality rates and severe long-term effects. The cytolytic protein α-hemolysin has repeatedly been shown to enhance the virulence of . Combined with an unhindered spread of multi drug-resistant strains, this has triggered research into novel anti virulence ( anti α-hemolysin) drugs. Their functionality will depend on our ability to identify infections that might be alleviated by such. We therefore saw a need for detection methods that could identify individuals suffering from infections where α-hemolysin was a major determinant. Molecular imprinted polymers were subsequently prepared on gold coated sensor chips. Used in combination with a surface plasmon resonance biosensor, α-hemolysin could therethrough be quantified from septic blood samples (n = 9), without pre-culturing of the infectious agent. The biosensor recognized α-hemolysin with high affinity (K = 2.75 x 10 M) and demonstrated a statistically significant difference ( < 0.0001) between the α-hemolysin response and potential sample contaminants. The detection scheme proved equally good, or better, when compared to antibody-based detection methods. This novel detection scheme constitutes a more rapid, economical, and user-friendly alternative to many methods currently in use. Heightening both reproducibility and sensitivity, molecular imprinting in combination with surface plasmon resonance (SPR)-technology could be a versatile new tool in clinical- and research-settings alike.

摘要

是脓毒症中的一种常见感染因子,与高死亡率和严重的长期影响有关。细胞溶蛋白α-溶血素已被反复证明可增强的毒力。再加上多药耐药株不受阻碍的传播,这引发了对新型抗毒力(抗α-溶血素)药物的研究。它们的功能将取决于我们识别可能通过这种方式缓解的感染的能力。因此,我们需要能够识别α-溶血素是主要决定因素的感染患者的检测方法。随后在金涂覆的传感器芯片上制备了分子印迹聚合物。与表面等离子体共振生物传感器结合使用,可从脓毒症血液样本(n = 9)中定量α-溶血素,而无需对感染因子进行预培养。该生物传感器对α-溶血素有高亲和力(K = 2.75 x 10 M),并且在α-溶血素反应与潜在样品污染物之间表现出统计学上的显著差异(<0.0001)。与基于抗体的检测方法相比,该检测方案同样出色,甚至更好。与许多当前使用的方法相比,这种新型检测方案构成了一种更快速、经济且用户友好的替代方案。分子印迹与表面等离子体共振(SPR)技术的结合提高了重现性和灵敏度,可能成为临床和研究环境中的一种多功能新工具。

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