Chimeric bivalent blood-pressure-reduction vaccine for human vascular smooth muscle cell L-type calcium channels and angiotensin 1-type receptors and application thereof
A technology of vascular smooth muscle and angiotensin, applied in the field of chimeric bivalent antihypertensive vaccine, can solve the problems of single target, feedback activation of renin-angiotensin system, high titer of vaccine carrier antibody, etc., and achieve good antihypertensive blood pressure effect, blood pressure lowering effect
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Embodiment 1
[0055] Example 1 Screening and Preparation of Four Amino Acid Sequences of Human Vascular Smooth Muscle Cell L-type Calcium Channel Epitope
[0056] Based on bioinformatics techniques such as amino acid hydrophilicity, antigenicity, and sequence space conformation to predict B cell epitopes, four amino acid sequences targeting human vascular smooth muscle cell L-type calcium channel epitopes were designed: VPAEDDPSPC, DSSKQTEAECK, DSHTEDKGPI , CAPESEPSNSTE. A PSSM-8 automatic peptide synthesizer (SHIMADZU, Japan) was used to synthesize peptides, and the purity of the synthesized peptides was analyzed by high performance liquid chromatography to reach more than 95%. The obtained peptides were lyophilized, aliquoted, placed in cryopreservation tubes, and stored at -80°C for later use.
Embodiment 2
[0057] Example 2 Combination Design of Target Molecular Epitopes Related to the Pathogenesis of Hypertension
[0058] Using the combination of the above four human vascular smooth muscle cell L-type calcium channel antigen epitopes and the human angiotensin type 1 receptor antigen CQ10 epitope / angiotensin II epitope sequence, various target molecular epitope combinations related to the onset of hypertension are formed as follows surface:
[0059]
[0060] Note: The amino acid sequence "GSG" is used to connect the above epitope sequences, and the epitope combination of target molecules related to hypertension is not limited to the combination of human vascular smooth muscle cell L-type calcium channel antigen epitope and human angiotensin 1 Type receptor antigen CQ10 epitope / angiotensin II combination; two existing hypertension-related target molecular epitopes can be composed.
Embodiment 3
[0061] Embodiment 3 recombinant hepatitis B core protein monomer molecular design
[0062] The epitope combinations of target molecules associated with the onset of hypertension in the above table can be inserted into any site between the 76th and 82nd amino acids in the amino acid sequence of the immunogenic carrier (SEQID No.1),
[0063] Alternatively, an amino acid sequence of any length between the 76th and 82nd amino acids in the amino acid sequence of the immunogenic carrier is replaced by a combination of target molecular epitopes related to the onset of hypertension; The combined form of CQ10-" is used as an example to construct recombinant hepatitis B core protein monomer molecules:
[0064] a. Insert the combination of "-CE12-CQ10-CE12-CQ10-" between the 80th and 81st amino acids in the immunogenic carrier amino acid sequence (SEQ IDNo.1): "--WVGTNMEDPA--CAPESEPSNSTEGSGAFHYESQGSGCAPESEPSNSTEGSGAFHYESQ--SRDLVVSYVN --";
[0065] b. The combination of "-CE12-CQ10-CE12...
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