An electrochemical lipopolysaccharide sensor based on an immobilized Toll-Like Receptor-4
Infections affect millions of people each year and yet methods to ascertain their cause can take more than 24h to be effective. This delay between the presentation with symptoms and the ability to make an informed decision about treatment can have adverse consequences, including death in severe case...
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Published in | Biosensors & bioelectronics Vol. 87; pp. 794 - 801 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
England
Elsevier B.V
15.01.2017
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Abstract | Infections affect millions of people each year and yet methods to ascertain their cause can take more than 24h to be effective. This delay between the presentation with symptoms and the ability to make an informed decision about treatment can have adverse consequences, including death in severe cases. Additionally, pathogen identification is a concern for public safety amid the growing threat of bioterrorism. Developing a detection system based on the immune system offers the advantage of broad specificity, while still remaining pertinent to human health. In this work, human Toll-Like Receptor-4 (TLR-4), a protein responsible for detecting lipopolysaccharide (LPS) of Gram-negative bacteria, was immobilized on both a large area and micro gold electrode via the tethering interaction of a modified Self-Assembled Monolayer (mSAM). In response to varying concentrations of its target, the protein-electrode combination showed a logarithmically proportional increased resistance to charge transfer from a solution-based redox probe, due to the formation of TLR-4 protein dimers. It also demonstrated excellent sensitivity to trace levels of Gram-negative bacteria, while remaining insensitive to both Gram-positive and viral challenges. Further characterization of our mSAM revealed that maintaining the appropriate receptor orientation on the electrode surface, mimicking TLR-4′s role in a cellular context, was essential in producing a responsive sensor.
•A Gram-negative bacterial sensor based on TLR-4 was developed.•The sensor responds logarithmically to LPS down to 1ng/mL and Gram-negative bacteria down to 100cells/mL.•The sensor responds specifically to LPS and Gram-negative bacteria.•A biomimetic approach to sensor construction was shown to give optimal sensor response. |
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AbstractList | Infections affect millions of people each year and yet methods to ascertain their cause can take more than 24h to be effective. This delay between the presentation with symptoms and the ability to make an informed decision about treatment can have adverse consequences, including death in severe cases. Additionally, pathogen identification is a concern for public safety amid the growing threat of bioterrorism. Developing a detection system based on the immune system offers the advantage of broad specificity, while still remaining pertinent to human health. In this work, human Toll-Like Receptor-4 (TLR-4), a protein responsible for detecting lipopolysaccharide (LPS) of Gram-negative bacteria, was immobilized on both a large area and micro gold electrode via the tethering interaction of a modified Self-Assembled Monolayer (mSAM). In response to varying concentrations of its target, the protein-electrode combination showed a logarithmically proportional increased resistance to charge transfer from a solution-based redox probe, due to the formation of TLR-4 protein dimers. It also demonstrated excellent sensitivity to trace levels of Gram-negative bacteria, while remaining insensitive to both Gram-positive and viral challenges. Further characterization of our mSAM revealed that maintaining the appropriate receptor orientation on the electrode surface, mimicking TLR-4's role in a cellular context, was essential in producing a responsive sensor. Infections affect millions of people each year and yet methods to ascertain their cause can take more than 24h to be effective. This delay between the presentation with symptoms and the ability to make an informed decision about treatment can have adverse consequences, including death in severe cases. Additionally, pathogen identification is a concern for public safety amid the growing threat of bioterrorism. Developing a detection system based on the immune system offers the advantage of broad specificity, while still remaining pertinent to human health. In this work, human Toll-Like Receptor-4 (TLR-4), a protein responsible for detecting lipopolysaccharide (LPS) of Gram-negative bacteria, was immobilized on both a large area and micro gold electrode via the tethering interaction of a modified Self-Assembled Monolayer (mSAM). In response to varying concentrations of its target, the protein-electrode combination showed a logarithmically proportional increased resistance to charge transfer from a solution-based redox probe, due to the formation of TLR-4 protein dimers. It also demonstrated excellent sensitivity to trace levels of Gram-negative bacteria, while remaining insensitive to both Gram-positive and viral challenges. Further characterization of our mSAM revealed that maintaining the appropriate receptor orientation on the electrode surface, mimicking TLR-4′s role in a cellular context, was essential in producing a responsive sensor. •A Gram-negative bacterial sensor based on TLR-4 was developed.•The sensor responds logarithmically to LPS down to 1ng/mL and Gram-negative bacteria down to 100cells/mL.•The sensor responds specifically to LPS and Gram-negative bacteria.•A biomimetic approach to sensor construction was shown to give optimal sensor response. |
Author | Chan, N.W.C. Renaud-Young, M. Mayall, R.M. Birss, V.I. |
Author_xml | – sequence: 1 givenname: R.M. surname: Mayall fullname: Mayall, R.M. organization: Department of Chemistry, University of Calgary, 2500 University Drive NW, Calgary, AB, Canada T2N 1N4 – sequence: 2 givenname: M. surname: Renaud-Young fullname: Renaud-Young, M. organization: Department of Chemistry, University of Calgary, 2500 University Drive NW, Calgary, AB, Canada T2N 1N4 – sequence: 3 givenname: N.W.C. surname: Chan fullname: Chan, N.W.C. organization: Defence Research and Development Canada, Suffield Research Centre, PO Box 4000, Station Main, Medicine Hat, AB, Canada T1A 8K6 – sequence: 4 givenname: V.I. surname: Birss fullname: Birss, V.I. email: birss@ucalgary.ca organization: Department of Chemistry, University of Calgary, 2500 University Drive NW, Calgary, AB, Canada T2N 1N4 |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/27657840$$D View this record in MEDLINE/PubMed |
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Keywords | Lipopolysaccharide Self-assembled monolayer Electrochemical biosensor Impedance spectroscopy Gram-negative bacteria Toll-Like Receptor-4 |
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SubjectTerms | Bacteria Biosensing Techniques - methods Biosensors Charge transfer Chromium Electrochemical biosensor Electrochemical Techniques - methods Electrodes Gram-negative bacteria Gram-Negative Bacteria - immunology Gram-Negative Bacteria - isolation & purification Gram-Negative Bacterial Infections - immunology Gram-Negative Bacterial Infections - microbiology Humans Immobilized Proteins - chemistry Immobilized Proteins - immunology Immune systems Impedance spectroscopy Lipopolysaccharide Lipopolysaccharides - analysis Lipopolysaccharides - immunology Models, Molecular Protein Multimerization Proteins Self-assembled monolayer Sensors Toll-Like Receptor 4 - chemistry Toll-Like Receptor 4 - immunology Toll-Like Receptor-4 |
Title | An electrochemical lipopolysaccharide sensor based on an immobilized Toll-Like Receptor-4 |
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