Natural killer T cell activator polypeptide and application thereof
A natural killer, activator technology, applied in the direction of peptides, peptide/protein components, medical preparations containing active ingredients, etc., can solve the problems that have not yet been developed, and achieve the effect of increasing the survival rate
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0015] Chemical Synthesis of Peptides
[0016] The peptides were synthesized using Fmoc chemistry. The synthesis reaction proceeds from the C-terminus to the N-terminus, and the Rink medium (available from Advanced ChemTech) has free amino groups, and the amino acids are connected sequentially. During each ligation step, the amino acid residues are activated, and the activation mixture contains 4 times as many HBTU, HOBt, DIEA and Fmoc-amino acids as there are free amino groups on the medium. After each amino acid linking reaction, a mixture of pyridine / acetic acid / N-methylimidazole (4:1:0.5) was used to block unlinked free amino groups for 10 min. After each amino acid ligation reaction and before the next amino acid is ligated, the Fmoc-group on the medium must be removed, and the Fmoc-group is removed using dimethylformamide containing 20% piperidine, which takes 15 minutes. Finally, after all amino acid residues are linked sequentially, the peptide is cleaved from the ...
Embodiment 2
[0019] IC50 values of natural killer T cell activator matrix metalloproteinase-2 in vitro.
[0020] Matrix metalloproteinase-2 is activated by cleaving the fluorescent substrate Mca-Arg-Pro-Lys-Pro-Val-Glu-Nval-Trp-Arg-Lys(Dnp)-NH 2 to detect (excitation wavelength=320 nm, emission wavelength=405 nm). Reactions were performed in 100 μl reactions at 37°C. At the beginning of the reaction, 4 μl of natural killer T cell activator 2 stock solution (1 ng / μl) was added to the reaction system, and the final concentration of the substrate was 10 μM. The calculated IC50 value was 2.05 μM.
Embodiment 3
[0022] In Vivo Viability of Natural Killer T Cell Activators Using an Endotoxic Shock Model
[0023] Before establishing the endotoxic shock model, we first determined the LD50 of LPS (E. coli 0111: B4, purchased from sigma company) in mice, which was 50 μg per mouse. In the experiment, we used 100 μg per mouse, In this way, all the mice in the control group died. In our previous scientific research work, we found that Regasepin2 (another peptide inhibitor, published) can improve the survival rate of C57BL / 6 mice during endotoxin shock. In order to establish endotoxin shock model in our mice, we did a positive control experiment with Regasepin2. The mice in the control group were injected with 100 μg of LPS, while the mice in the Regasepin2 experimental group were injected with 0.7 mg of polypeptide 5 minutes after LPS injection. By making a Kaplan-Meier survival curve, it was found that Regasepin2 can effectively protect mice injected with 100 μg and improve the survival ra...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com