A novel peptide ligand for modifying quantum dots
A technology of polypeptide ligands and quantum dots, applied in the direction of peptides, can solve the problems of affecting the tertiary structure of the target protein activity, difficult to improve the binding force of the polypeptide sequence, slow binding speed, etc., to solve the problems of insufficient stability, fast binding speed, The effect of good binding affinity
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Embodiment 1
[0019] The method of the present invention adopts the conventional solid-phase Fmoc method, that is, the monomer amino acid protected by Fmoc on the solid-phase resin is deprotected to expose the amino group, and forms a peptide bond with the carboxyl group of the amino acid in the solution through a condensation reaction, thereby linking the amino acid to the On the resin, the peptide chain is extended from the C-terminus to the N-terminus.
[0020] 1. Basic materials:
[0021] (1) Resin and linking molecule: the resin selected by the solid-phase Fmoc method is Rink resin. This kind of resin has very good swelling property, which can make the condensation reaction between the peptide chains better, and there is enough network space to meet the growing peptide chains. HBTU and HOBt are used as linking molecules to immobilize the polypeptide molecules on the resin.
[0022] (2) Monomer: The monomer used in the synthesis is a chemically modified α-amino acid.
[0023] 2. Re...
Embodiment 2
[0044] Refer to Example 1 for the steps of polypeptide synthesis. According to DDG(NH) 6 The order of the sequence is synthesized from right to left, and the synthetic novel peptide ligand sequence is as follows:
[0045] ATTO-DDG(NH) 6
Embodiment 3
[0047] Refer to Example 1 for the steps of polypeptide synthesis. According to EES(NH) 6 The order of the sequence is synthesized from right to left, and the synthetic novel peptide ligand sequence is as follows:
[0048] ATTO-EES(NH) 6
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