Application of human polypeptide in preparation of immune regulator
An immunomodulator, human technology, applied in the fields of peptide/protein components, medical preparations containing active ingredients, allergic diseases, etc.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0024] Example 1: Preparation of hIAPP
[0025] (1) The amino acid sequence of human amylin (islet amyloid polypeptide, hIAPP / Amylin):
[0026] KCNTATCATQRLANFLVHSSNNFGAILSSTNVGSNTY
[0027] (2) Synthesis and purification of hIAPP:
[0028] full-length peptide hIAPP 1-37 Provided by the Keck Biotechnology Center, Yale University, New Haven, CT, the center uses t-boc chemistry to synthesize hIAPP, and uses reversed-phase high-pressure liquid chromatography to purify, with a purity of more than 99.95%.
[0029] (3) Preparation of hIAPP solution
[0030] The lyophilized peptide hIAPP was pretreated with a 1:1 mixture of trifluoroacetic acid (TFA) and hexafluoroisopropanol (HFIP). Transfer the dissolved hIAPP to a new tube and let the HFIP / TFA evaporate under a gentle flow of nitrogen for 5-10 minutes. The lyophilized peptide was dissolved in 0.5% acetic acid solution to prepare a 50 mmol / L stock solution. Before use, prepare fresh hIAPP solution by diluting the stock solu...
Embodiment 2
[0031] Example 2: Effect of hIAPP on mouse splenocytes and human peripheral blood mononuclear cells
[0032] 2.1 Primary mouse spleen cell culture
[0033] Six clean-grade C57BL / 6 mice aged 5-6 months were provided by the Animal Experiment Center of the school. The mice were anesthetized and sacrificed. The spleen was removed under aseptic conditions, ground to prepare a fresh single-cell suspension, and then buffered with ammonium acid hemolysis. solution (BD company kit) to treat splenocytes, remove red blood cells, wash 3 times, and adjust the cell concentration to 5×10 4 cells / ml. Primary splenocytes were cultured using RPMI medium 1640 from Invitrogen Gibco, USA. Add 1, 5, 10, 50, 100, 500, 1000 or 10000 nmol / L hIAPP freshly prepared solutions to splenocytes (100ml) on a 96-well plate, respectively, and control group without hIAPP, in CO 2 The incubators were incubated for 24, 48, or 72 hours, respectively. Finally, Olympus phase contrast microscope CKX41-32PH was u...
Embodiment 3
[0039] Example 3: hIAPP induces human PBMCs to transform into CD4+CD25+Foxp3+ regulatory T cells
[0040] 3.1 Isolation of human PBMC
[0041] 300 ml of peripheral blood (900 ml in total) were collected from 3 healthy blood donors, anticoagulated with ethylenediaminetetraacetic acid (EDTA), and PBMCs were separated using the density gradient method. After red blood cell lysis and 3 washes, PBMCs were counted up to 5′10 6 cells / ml;
[0042] 3.2 hIAPP induced PBMC
[0043] At 37°C, hIAPP solution (10 nmol / L) was used to incubate for 24 hours, and the control group was the same except that hIAPP was not added;
[0044] 3.3 Detection of CD4+CD25+Foxp3+ regulatory T cells by flow cytometry
[0045] Treated human PBMCs were reacted with T cell surface antibodies CD4 and CD25 at 37°C for 30 minutes, and then washed with PBS buffer. Next, add BD Foxp3 buffer at 50:1 and fix for 10 minutes. The fixed PBMCs were permeable with BD Perm buffer for 30 minutes, and then washed twic...
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