Quantum dot-polypeptide compound with linear polycaprolactone joint arm
A technology of polypeptide complexes and polycaprolactone, which is applied in the fields of peptides, peptide sources, viral peptides, etc., can solve the problems of unreported quantum dot complexes.
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Embodiment 1
[0030] Synthesis of Adhesive Antigen-8-unit Caprolactone-Quantum Dot Complex of Porcine Enterotoxin-derived Escherichia coli K88ac: 6-methylene imidazole caprolactone was selected as the caprolactone monomer.
[0031]
[0032] Mix 0.01mol of porcine enterotoxin-derived Escherichia coli K88ac adhesion antigen and 0.08mol of 6-methylene imidazole caprolactone in DMF solution, slowly adjust the pH to 8.0, stir at room temperature for 2 hours, and pour the reaction solution into n-hexane A white colloidal solid was precipitated out, and the filter cake was vacuum-dried after filtration.
[0033] CdSe / ZnS shell quantum dots were selected and dispersed in phosphate buffer at room temperature with a quantum dot concentration of 0.1mol / L. Use N-hydroxysulfosuccinic acid imide as the activator at a concentration of 20 mol / L, react on a shaking table at room temperature for 1 hour, wash with neutral acetonitrile to remove excess activator. Add the antibody polypeptide chain-caprolac...
Embodiment 2
[0035] Synthesis of hepatitis B virus core antigen-300 unit caprolactone arm-quantum dot complex: 5-methylenethiazole caprolactone is selected as the caprolactone monomer.
[0036]
[0037] Mix 0.001 mol of hepatitis B virus core antigen and 0.30 mol of 5-methylenethiazol caprolactone in water / acetonitrile solution, slowly adjust the pH to 8.0, stir at room temperature for 2 hours, pour the reaction solution into n-hexane to precipitate white Gummy solid, filter and dry the filter cake in vacuo.
[0038] CdSe / ZnS shell quantum dots were selected and dispersed in phosphate buffer at room temperature with a quantum dot concentration of 0.1mol / L. Use N-hydroxysulfosuccinic acid imide as the activator at a concentration of 20 mol / L, react on a shaking table at room temperature for 1 hour, wash with neutral acetonitrile to remove excess activator. Add the above-mentioned phosphate buffer, and centrifuge the resulting reaction product at a speed of 5,000 rpm in a high-speed cent...
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