生物分子相互作用- DNA -抗菌肽结合的无标记检测

P. Fojan, K. R. Jensen, L. Gurevich
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引用次数: 3

摘要

在研究和临床应用中,对表面或局部平面生物传感器的兴趣正在迅速增长。基于等离子体的传感器提供极高的灵敏度,仅次于涉及荧光标记的光学检测技术,但不需要标记分子。特别是,表面等离子体共振(SPR)传感器已被证明适用于食品安全控制、体液中各种疾病标志物的无标签筛选,以及重症监护环境中药物水平的实时连续监测。我们设想将这种传感器集成到无线通信基础设施中,用于电子健康和环境监测应用。医院环境中的重要威胁之一是不受普通抗生素影响的多重耐药生物。多重耐药感染的增长激发了人们对抗菌肽的兴趣,这些抗菌肽对包括细菌、真菌和病毒在内的广泛感染具有活性,并且被证明能够单独或与常规抗生素联合治疗多重耐药感染。在本文中,我们展示了基于等离子体的生物传感器在抗菌肽IL4和DNA相互作用研究中的应用。我们的研究结果表明,IL4和DNA之间的高亲和力结合从而阻止DNA复制并最终杀死受影响的细胞。我们推测,这是常见的一大类抗菌肽,可以是一个关键的点解释其广泛的活性对抗各种病原体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Label-free detection of biomolecular interaction — DNA — Antimicrobial peptide binding
Interest to biosensors employing surface or localized plamons is rapidly growing both in research and clinical application. Plasmon-based sensors offer extremely high sensitivity, only second to the optical detection techniques involving fluorescent labeling, but without the necessity to label the molecule. In particular, surface plasmon resonance (SPR) sensors have been already demonstrated suitable for food-safety control, label-free screening for various disease markers in bodily fluids, as well as for real-time continuous monitoring of drug levels in intensive care environment. We envisage such sensors to be integrated into wireless communication infrastructure for e-health and environmental monitoring applications. One of the important threats in hospital environment is multi-resistant organisms that are not affected by common antibiotics. The growth of multi-resistant infections spurred an interest in Antimicrobial peptides that are active against broad range of infections including bacteria, fungi and viruses and were shown to be capable of treating multi-resistant infection either alone or in combination with the conventional antibiotics. In this paper, we demonstrate an application of plasmon based biosensors to the study of the interaction of Antimicrobial peptide IL4 and DNA. Our results indicate high affinity binding between IL4 and DNA thereby preventing DNA replication and eventually killing the affected cell. We speculate that this is common for a large class of Antimicrobial peptides and can be a key point explaining their broad range of activity against various pathogens.
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