Function of surfactant, and signal amplification method for SPR (Surface Plasma Resonance) detection on low molecular weight substances
A surfactant and surface plasmon technology, applied in the field of bioinformatics, can solve problems such as complex experimental processes, and achieve the effect of high experimental repeatability and easy operation
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Embodiment 1
[0120] Example 1 Amplification of SPRI signals by treating the substrate small molecule 4-nitrophenyl octanoate (4-Nitrophenyl octanoate) with surfactant Tween-80
[0121] 1. Immobilize 100ug / ml lipase CalB on the surface of the SPRI chip, and use 200ug / ml bovine serum albumin BSA as a negative control;
[0122] 2. Prepare PBS+0.05% Tween-80 buffer;
[0123] 3. Fix the chip on the SPRI device, and scan the intensity of the fixed positions of lipase CalB and bovine serum albumin BSA through the program selection, and pass the surface into PBS+0.05%Tween-80 buffer for baseline scanning, such as figure 1 Baseline shown;
[0124] 4. Use the prepared PBS+0.05%Tween-80 buffer to prepare the substrate small molecule 4-nitrophenyl octanoate
[0125] Diluted from 10mM of the mother solution to 0.25mM to obtain sample 1;
[0126] 5. Inject sample 1 at a binding rate of 2ul / s, such as figure 1 Combined with the curve shown;
[0127] 6. Flush with PBS+0.05% Tween-80 buffer until the ...
Embodiment 2
[0129] Example 2 Amplification of SPRI signal by treating the substrate small molecule 4-nitrophenyl octanoate (4-Nitrophenyl octanoate) with surfactant Tween-80
[0130] 1. Immobilize 100ug / ml lipase CalB on the surface of the SPRI chip, and use 200ug / ml bovine serum albumin BSA as a negative control;
[0131] 2. Prepare PBS+0.05% Tween-80 buffer;
[0132] 1. Fix the chip on the SPRI device, select the fixed positions of lipase CalB and bovine serum albumin BSA for intensity scanning, and pass the surface into PBS buffer for baseline scanning, such as image 3 Baseline shown;
[0133] 2. Dilute the substrate small molecule 4-nitrophenyl octanoate from the mother solution 10mM to 0.25mM with the prepared PBS+0.05%Tween-80 buffer solution to obtain sample 1;
[0134] 3. Pass through sample 1 at a binding rate of 2ul / s, and the binding time is 400s, such as image 3 Combined with the curve shown;
[0135] 4. Flush with PBS buffer until the baseline is stable, such as image...
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