A controllable array preparation method of microsensors using tobacco mosaic virus as a template
A tobacco mosaic virus and micro-sensor technology, applied in instruments, scientific instruments, measuring devices, etc., can solve the problems of expensive equipment, complex preparation process, difficult to achieve complex microstructure preparation and controllable arraying
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Embodiment 1
[0042] Example 1: Preparation method of piezoelectric sensor array based on tobacco mosaic virus
[0043] Step 1: Use phage display technology to obtain polypeptides and corresponding gene sequences that can specifically bind to barium titanate (BTO) piezoelectric nanoparticles
[0044] A: Take an appropriate amount of barium titanate (BTO) nanoparticle dispersion, place it in the buffer solution containing the M13 phage library, shake and mix at room temperature for 2 hours, so that the M13 phage and barium titanate nanoparticles are fully mixed;
[0045] B: centrifuge the above mixed solution for 40min at 3500rpm, remove the supernatant;
[0046] C: Rinse the precipitate 3 times with a buffer to remove the phages that are not firmly adsorbed;
[0047] D: Elute the phage that adsorbs specific functional nanoparticles, and place it in Escherichia coli culture solution for enrichment and cultivation for 30 minutes;
[0048] E: Perform high-throughput sequencing on the enriche...
Embodiment 2
[0072] Example 2: Preparation method of ammonia sensor array based on tobacco mosaic virus
[0073] Step 1: Use phage display technology to obtain a compound that can specifically bind to titanium dioxide (TiO 2 ) polypeptides of piezoelectric nanoparticles and their corresponding gene sequences
[0074] A: Take an appropriate amount of titanium dioxide (TiO 2 ) nanoparticle dispersion, which is placed in the buffer containing the M13 phage library, and shaken and mixed at room temperature for 2 hours to make the M13 phage and titanium dioxide (TiO 2 ) nanoparticles are fully mixed;
[0075] B: centrifuge the above mixed solution for 40min at 3500rpm, remove the supernatant;
[0076] C: Rinse the precipitate 3 times with a buffer to remove the phages that are not firmly adsorbed;
[0077] D: Elute the phage that adsorbs specific functional nanoparticles, and place it in Escherichia coli culture solution for enrichment and cultivation for 30 minutes;
[0078] E: Perform hi...
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