Nanoparticle cluster assembling method with micro magnetic beads as growth template and DNA frame as guide carrier
A nanoparticle and growth template technology, which is applied in nanotechnology, nanotechnology, nanostructure manufacturing, etc., can solve the problems of low yield, multiple purifications, and many by-products, and achieve high yield, rapid preparation, and short time. Effect
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Embodiment 1
[0030] A method for assembling nanoparticle clusters using micro-magnetic beads as a growth template and a DNA framework as a guide carrier of the present invention comprises the following steps:
[0031] (1) The octahedral DNA origami framework was selected, mixed with the modified 10 nm gold balls at a ratio of 1:1.3 and quenched at a constant speed for 10 hours, and purified by agarose gel electrophoresis to obtain a DNA origami complex carrying gold balls Objects, that is, growth units assembled by nanoparticle clusters; the DNA origami framework is an octahedral DNA origami framework, and the nucleotide sequences of the octahedron DNA origami framework are as SEQ ID NO: 1, 2, 3, 4... The nucleotide sequence shown at 120.
[0032] (2) Mix the first layer of growth units with the DNA-modified micro-magnetic bead solution, and react at room temperature for 4 hours. After the reaction, use a magnet to wash with buffer three times to remove unconnected growth units, and then a...
Embodiment 2
[0034] The difference between Example 2 and Example 1 is that in step (1), the octahedral DNA origami framework is selected, mixed with the modified 10nm gold balls at a ratio of 1:1.3, and quenched at a constant speed for 10 hours, and passed through agarose After gel electrophoresis purification, DNA origami complexes carrying gold spheres, i.e. growth units assembled by nanoparticle clusters, were obtained;
[0035] In step (2), mix the first layer of growth units with the DNA-modified micro-magnetic bead solution, and react at room temperature for 8 hours. After the reaction, use a magnet to wash with buffer three times to remove unconnected growth units, and then Add the second layer of growth unit, and the constant temperature reaction time on the metal mixer is 12 hours, and the rotation speed is 1000 rpm. After the reaction is completed, it is also cleaned with a magnet, and then the third layer of growth unit is added, and the constant temperature reaction time is 12 h...
Embodiment 3
[0037] The difference between embodiment 3 and embodiment 1 is:
[0038] In step (1), the octahedral DNA origami framework was selected, mixed with the modified 10 nm gold balls at a ratio of 1:1.3 and quenched at a constant speed for 10 hours, and purified by agarose gel electrophoresis to obtain gold balls carrying DNA origami complexes, growth units assembled by nanoparticle clusters;
[0039]In step (2), mix the first layer of growth units with the DNA-modified micro-magnetic bead solution, and react at room temperature for 8 hours. After the reaction, use a magnet to wash with buffer three times to remove unconnected growth units. Then add the second layer of growth unit, the constant temperature reaction time is 12 hours on the metal mixer, and the rotation speed is 1000 rpm. After the reaction is completed, it is also cleaned with a magnet, and then the third layer of growth unit is added, and the constant temperature reaction time is 12 hours. , the rotating speed is ...
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