Preparation method and application of recombinant protein and monoclonal antibody thereof
A recombinant protein and protein technology, which is applied in the field of early diagnosis of acute myocardial infarction and the preparation of cardiac fatty acid binding protein monoclonal antibody, can solve the problems of low expression level, poor specificity of monoclonal antibody, and distortion of detection results, etc., to improve the expression level , improve sensitivity, enhance the effect of stimulation
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Embodiment 1
[0013] Example 1: Selection of dominant epitopes of heart-type fatty acid binding protein
[0014] Taking human heart-type fatty acid binding protein as the target antigen, using the biological software DNAssist2.0 to analyze the hydrophilicity and antigenicity of the epitope sequence, and select the A dominant epitope (SEQ ID No: 2) and the B dominant antigenic epitope (SEQ ID No: 3). At the same time, the sequence comparison results showed that the selected two dominant antigenic epitopes A and B have high sequence specificity and no obvious homology with other protein sequences.
Embodiment 2
[0015] Example 2: Concatenation of Cardiac Fatty Acid Binding Protein Predominant Epitopes
[0016] In order to enhance the stimulation of the selected antigenic epitopes to the immune system of mice to facilitate subsequent experiments, the two dominant antigenic epitope sequences of heart-type fatty acid binding protein A and B were respectively repeated and then passed through the flexible fragment (four consecutive glycines) Linked to obtain the amino acid sequence of the recombinant protein, the specific sequence of which is shown in SEQ ID No: 1 in the sequence table.
Embodiment 3
[0017] Embodiment 3: optimize the nucleotide sequence of coding recombinant protein
[0018] In order to improve the expression of the recombinant protein in E. coli, under the premise that the amino acid sequence of the recombinant protein remains unchanged, the amino acid sequence encoding the recombinant protein is converted into the corresponding nucleotide sequence according to the preferred codons of E. coli. The specific sequence is shown in the sequence table Shown in SEQ ID No: 4, after adding the nucleotide sequences corresponding to the enzyme cutting sites BamHI and EcoRI in its upstream and downstream, respectively, it was synthesized by Hangzhou Xianzhi Biotechnology Co., Ltd. The synthesized target gene was cloned in the pMD19-T vector (Bao Bioengineering Dalian Co., Ltd.).
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