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Updated: Feb 1, 2026

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Detection of Toxin Translocation into the Host Cytosol by Surface Plasmon Resonance
Published on: January 3, 2012
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Detection of Autoantibodies to Complement Components by Surface Plasmon Resonance-Based Technology
Remi Noe1,2,3, Sophie Chauvet1,2,3,4, Shambhuprasad K Togarsimalemath1,2,3
1INSERM, UMR_S 1138, Centre de Recherche des Cordeliers, Paris, France.
Methods in Molecular Biology (Clifton, N.J.)
|December 13, 2018
Summary
The complement system protects against pathogens but can harm tissues when overactivated. This study presents a new method to detect autoantibodies against complement proteins, aiding in diagnosing related diseases.
Area of Science:
- Immunology
- Pathology
- Biochemistry
Background:
- The complement system is crucial for innate immunity but its dysregulation causes tissue damage, particularly in renal diseases like lupus nephritis.
- Autoantibodies against complement components (e.g., C1q, Factor H, C3, Factor B) are implicated in pathological complement overactivation.
- Accurate detection of these autoantibodies is vital for diagnosing and managing complement-mediated diseases.
Purpose of the Study:
- To describe a novel method for real-time detection of anti-complement autoantibodies.
- To evaluate the utility of surface plasmon resonance (SPR) technology for this purpose.
Main Methods:
- Utilized surface plasmon resonance (SPR) technology for label-free detection of anti-complement autoantibodies.
- Assessed binding efficacy and stability of antigen-antibody complexes in real time.
Main Results:
- Demonstrated the capability of SPR to detect autoantibodies against key complement components.
- Provided a method for label-free, real-time evaluation of autoantibody interactions with complement targets.
Conclusions:
- The described SPR-based method offers a sensitive and efficient approach for detecting anti-complement autoantibodies.
- This technology can aid in the diagnosis and understanding of complement-related pathologies.
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