New nano-gold compound and preparation method thereof
A nano-gold, composite technology, applied in the direction of nanotechnology, nanotechnology for materials and surface science, nanotechnology, etc., can solve the problems of lack of versatility, waste of raw materials, limited application, etc.
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Embodiment 1
[0107] Example 1 compares the differences in the assembly of BSPP-protected gold nanoparticles and block DNA under different pH conditions.
[0108] Experimental materials used: 10nm gold nanoparticles protected by BSPP, block DNA:
[0109] DNA: FAM-PolyA: AAAAAAA-FAM
[0110] Experimental principle: FAM-polyA is a piece of DNA composed of seven adenine nucleotides bound with a FAM fluorescent group at the 3' end. In the solution state, there is a strong fluorescence emission. When DNA is adsorbed on the surface of gold nanoparticles, the fluorescence is quenched, thereby reducing the fluorescence intensity in the solution. The amount of DNA adsorbed on the surface of gold nanoparticles was qualitatively analyzed by how much the fluorescence intensity decreased.
[0111] Experimental steps:
[0112] FAM-labeled polyADNA (FAM-polyA) and BSPP-protected gold nanoparticles were mixed, then citrate buffer solution with pH 3 or 7 was added, and the fluorescence value of the syste...
Embodiment 2
[0114] Embodiment 2 compares the assembly situation of the nanogold protected by BSPP to block DNA in different pH ranges
[0115] Experimental materials used: 10nm gold nanoparticles protected by BSPP:
[0116] polyA80-DNA:
[0117] AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAATACGACGTGTGACCATGCA (SEQ ID NO.: 10)
[0118] Experimental procedure: Mix block DNA (polyA80-DNA) and BSPP-protected gold nanoparticles (100nM) at a ratio of 5:1, add trisodium citrate buffer (2.0; 3.0; 4.0; 5.0; 6.0; 7.0 ; 8.0), after standing for 10 minutes, carry out agarose gel electrophoresis characterization.
[0119] The above experimental results show that (see Figure 4 ), the block DNA can be assembled and adsorbed on the BSPP-protected gold nanoparticles within 10 minutes only under acidic conditions (pH2-4).
Embodiment 3
[0120] The assembly situation of polyA80-DNA in the scope of embodiment 3pH2.0-4.0
[0121] Experimental procedure: Mix block DNA (polyA80-DNA) and BSPP-protected gold nanoparticles (100nM) at a ratio of 5:1, add trisodium citrate buffer (2.0; 2.4; 2.8; 2.9; 3.0; 3.1 ; 3.2; 3.3; 3.4; 3.5; 3.6; 4.0), after standing for 10 minutes, agarose gel electrophoresis was performed.
[0122] The above experimental results show that (see Figure 5 ), in the range of pH 2-3.6, the higher the pH value, the fewer the number of block nucleic acids bound on the gold nanoparticles. In the case of pH 3.1, polyA80-DNA can achieve 90% single binding yield. The amount of binding assembly gradually increases with the decrease of pH, and quantitative binding such as double binding or triple binding can be achieved when the pH is lower than 3.1.
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