Optical Aptamer-Based Cytokine Nanosensor Detects Macrophage Activation by Bacterial Toxins

被引:0
|
作者
Ryan, Amelia K. [1 ]
Rahman, Syeda [1 ]
Williams, Ryan M. [1 ,2 ]
机构
[1] CUNY, City Coll New York, Dept Biomed Engn, New York, NY 10031 USA
[2] CUNY, Grad Ctr, PhD Program Chem, New York, NY 10016 USA
来源
ACS SENSORS | 2024年 / 9卷 / 07期
基金
美国国家卫生研究院;
关键词
IL-6; DNA aptamer; inflammation; nanocarbon; SWCNT; fluorescence; WALLED CARBON NANOTUBES; DNA APTAMER; ALZHEIMERS-DISEASE; LABEL-FREE; INTERLEUKIN-6; FLUORESCENCE; APTASENSOR; PARTITION; SENSORS;
D O I
10.1021/acssensors.4c00887
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Overactive or dysregulated cytokine expression is a hallmark of many acute and chronic inflammatory diseases. This is true for acute or chronic infections, neurodegenerative diseases, autoimmune diseases, cardiovascular diseases, cancer, and others. Cytokines such as interleukin-6 (IL-6) are known therapeutic targets and biomarkers for such inflammatory diseases. Platforms for cytokine detection are, therefore, desirable tools for both research and clinical applications. Single-walled carbon nanotubes (SWCNT) are versatile nanomaterials with near-infrared fluorescence that can serve as transducers for optical sensors. When functionalized with an analyte-specific recognition element, SWCNT emission may become sensitive and selective toward the desired target. SWCNT-aptamer sensors are easily assembled, inexpensive, and biocompatible. In this work, we introduced a nanosensor design based on SWCNT and a DNA aptamer specific to IL-6. We first evaluated several SWCNT-aptamer constructs based on this simple direct complexation method, wherein the aptamer both solubilizes the SWCNT and confers sensitivity to IL-6. The sensor limit of detection, 105 ng/mL, lies in the relevant range for pathological IL-6 levels. Upon investigation of sensor kinetics, we found rapid response within seconds of antigen addition which continued over the course of 3 h. We found that this sensor construct is stable and the aptamer is not displaced from the nanotube surface during IL-6 detection. Finally, we investigated the ability of this sensor construct to detect macrophage activation caused by bacterial lipopolysaccharides (LPS) in an in vitro model of disease, finding rapid and sensitive detection of macrophage-expressed IL-6. We are confident that further development of this sensor will have novel implications for diagnosis of acute and chronic inflammatory diseases, in addition to contributing to the understanding of the role of cytokines in these diseases.
引用
收藏
页码:3697 / 3706
页数:10
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