High-motion-activity polypeptide capable of inhibiting cocaine induction and application thereof
A technology of polypeptide and activity, applied in the field of polypeptide with high motor activity
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Embodiment 1
[0047] Example 1, PKD1 (protein kinase D1) phosphorylation D1RC terminal specific phosphorylation site identification
[0048] 1. Preparation of GST-tagged protein
[0049] Type I dopamine receptor (hereinafter referred to as D1R) has a full length of 446 amino acids and is a typical G protein-coupled receptor with a classic seven-transmembrane structure. Therefore, the D1 receptor is segmented and defined as the N-terminus, respectively. One transmembrane domain, first intracellular loop, second transmembrane domain, first extracellular loop, third transmembrane domain, second intracellular loop, fourth transmembrane domain, second extracellular loop , the fifth transmembrane domain, the third intracellular loop, the sixth transmembrane domain, the third extracellular loop, the seventh transmembrane domain, the C-terminus ( figure 1 a).
[0050] The amino acid sequence of the type I dopamine receptor is sequence 1 in the sequence list, and the nucleotide sequence is sequenc...
Embodiment 2
[0099] Example 2, the acquisition of Tat-D1R-CT-S421 and its application in inhibiting high motor activity induced by cocaine
[0100] 1. Acquisition of Tat-D1R-CT-S421
[0101] TAT (transcriptional activator protein) penetrating peptide is one of the transmembrane delivery carriers, which can introduce covalently linked polypeptides, proteins, DNA and other molecules into cells across the membrane, and even pass through the blood-brain barrier. Without damage, it has been widely used in the fields of cell biology, gene therapy and pharmacy. According to the serine 421 of the phosphorylation site of PKD1 in D1R-CT, 14 amino acid residues including the phosphorylation preference sequence of PKD1 were selected to construct a fusion peptide with membrane penetrating ability——Tat-D1R-CT-S421. The serine at position 421 in the target sequence was mutated to alanine, ie Tat-D1R-CT-S421A was used as a control.
[0102] The amino acid sequence of Tat-D1R-CT-S421 is the sequence 2 in...
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