研究目的
Development of a label-free real-time SPR optical method for the sensing of BoNT/A with carboxymethyldextran modified gold chip (CM5 chip).
研究成果
A label free real time SPR detection methodology for BoNT/A was developed using a carboxymethyldextran modified sensor chip. The effective interaction between the antigen and antibody was confirmed based on EIS data. The LOD of the developed method is 0.045 fM. The SPR sensor gram of the binding of BoNT/A with immobilized SV confirmed the biological activity of purified protein. The kinetic parameters such as KD and Bmax values were calculated. The negative value of change in Gibbs free energy indicates the spontaneous nature of interaction of BoNT/A antigen with immobilized antibody and SV and the positive value of ?H revealed the interaction of BoNT/A with immobilized antibody as endothermic.
研究不足
The study focuses on the detection of BoNT/A using SPR and does not cover other serotypes of botulinum neurotoxins. The method's sensitivity and specificity in complex matrices were not extensively evaluated.
1:Experimental Design and Method Selection:
SPR assays were conducted using a two channel cuvette based electrochemical surface plasmon resonance system on CM5 chip using 10 mM PBS (pH
2:4) as running buffer. Sample Selection and Data Sources:
Rat brain fractions containing Synaptic Vesicles (SVs) were obtained in one step. rBoNT/A-HCC gene was cloned, expressed and purified and BoNT/A antibody was raised.
3:List of Experimental Equipment and Materials:
SPR system (Autolab ESPRIT, Ecochemie B.V., The Netherlands), CM5 chip, EDC, NHS, PBS, sodium acetate, ethanolamine, HCl, etc.
4:Experimental Procedures and Operational Workflow:
Immobilization of BoNT/A antibody and SV protein on CM5 chip, interaction of BoNT/A with immobilized antibody and SV, optimization of experimental parameters (temperature and pH).
5:Data Analysis Methods:
Kinetic and thermodynamic parameters were evaluated using kinetic evaluation software version 5.1.
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Autolab ESPRIT
Ecochemie B.V.
SPR assays were conducted using a two channel cuvette based electrochemical surface plasmon resonance system.
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CM5 chip
Xantec Bioanalytics
Used for SPR measurements with a thickness of 50 nm (20 nm carboxymethyldextran coating +30 nm gold).
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EDC
Fluka
Used for the activation of carboxyl groups on CM5 chip.
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NHS
Fluka
Used for the activation of carboxyl groups on CM5 chip.
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PBS
Fluka
Used as running buffer in SPR assays.
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sodium acetate
Fluka
Used in the preparation of buffer solutions.
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ethanolamine
Fluka
Used for blocking of unreacted NHS-ester groups on CM5 chip.
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HCl
Fluka
Used for regeneration of the sensor surface.
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glacial acetic acid
Sigma-Aldrich
Used in the preparation of buffer solutions.
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glycine
Sigma-Aldrich
Used in the preparation of buffer solutions.
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NaOH
Sigma-Aldrich
Used in the preparation of buffer solutions.
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Julabo HE-4
Germany
Water bath used to control the temperature of cuvette.
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EUTECH instrument pH meter
pH-1500
Singapore
Used to measure the pH of the buffers.
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