Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

A kind of enzymolysis-resistant antimicrobial peptide i9h12 and its preparation method and application

An I9H12, anti-enzyme technology, which is applied in the preparation method of peptides, antibacterial drugs, antifungal agents, etc., can solve the problem of less antibacterial peptides, and achieve the effects of high inhibitory effect, low hemolytic toxicity, and simple experimental techniques

Active Publication Date: 2021-12-14
NORTHEAST AGRICULTURAL UNIVERSITY
View PDF5 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] At present, thousands of antimicrobial peptides have been extracted or newly designed, but few antimicrobial peptides have been put into practical use as antibiotic substitutes

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • A kind of enzymolysis-resistant antimicrobial peptide i9h12 and its preparation method and application
  • A kind of enzymolysis-resistant antimicrobial peptide i9h12 and its preparation method and application
  • A kind of enzymolysis-resistant antimicrobial peptide i9h12 and its preparation method and application

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0012] Antimicrobial Peptide Design:

[0013] The amino acid sequence of the antimicrobial peptide I9H12 is:

[0014] Ile His His Ile His His Ile Ile His His Ile His His Ile Ile His His Ile His His His Ile-NH2

1 5 10 15 20 21

[0015] Referring to the properties of amino acids, while avoiding the cleavage sites of major proteases in the body as much as possible, the hydrophobic amino acid isoleucine (Ile) and the positively charged amino acid histidine (His) were selected as the main amino acids to newly design the I9H12 antimicrobial peptide. The carboxyl terminus of the peptide is amidated to add a positive charge and increase the stability of the peptide. The sequences of the antimicrobial peptides are shown in Table 1.

[0016] Table 1 Main parameters of newly designed peptides

[0017]

[0018] I9H12 is a small peptide with 21 amino acids, the charge number is +13 at pH 6.0, and the hydrophobic amino acid ratio is 0.4286.

Embodiment 2

[0020] The above-mentioned antimicrobial peptides were synthesized using a peptide synthesizer. The method was solid-phase chemical synthesis, and the specific steps were:

[0021] 1. The preparation of antimicrobial peptides is carried out one by one from the C-terminal to the N-terminal, and is completed by a peptide synthesizer. First, Fmoc-X (X is the first amino acid at the C-terminal of each antimicrobial peptide) is inserted into Wang resin, and then the Fmoc group is removed to obtain X-Wang resin; then Fmoc-Y-Trt-OH (9 -Fmoxy-trimethyl-Y, Y is the second amino acid at the C-terminus of each antimicrobial peptide); according to this procedure, it is synthesized from the C-terminus to the N-terminus until the synthesis is completed, and the side of the Fmoc group is removed chain protection resin;

[0022] 2. Add a cleavage reagent to the peptide resin obtained above, react at 20°C for 2 hours in the dark, filter; precipitate with TFA (trifluoroacetic acid) and wash, m...

specific Embodiment approach 3

[0025] Detect the antibacterial activity, hemolytic activity and protease hydrolysis ability of the designed and synthesized antimicrobial peptide in vitro;

[0026] 1. Determination of antibacterial activity: The minimum inhibitory concentration of several antibacterial peptides was determined by the micro broth dilution method. Bacterial single colonies were picked and cultured overnight in MHB medium, and transferred to new MHB to grow to mid-logarithmic phase. Then the above bacterial solution was centrifuged and resuspended in MHB adjusted to pH 6.0 to a final concentration of 1 × 10 5 CFUml -1 , and transferred to a 96-well plate, 50 μl per well, and the fungi were diluted in RPMI 1640 (pH=6.0) medium containing morpholine propanesulfonic acid (MOPS). 50 μl of BSA (pH=6.0) containing different concentrations of peptides were added to the above-mentioned 96-well plate, and the final peptide concentration in the 96-well plate ranged from 0.125 to 64 μM. After incubating...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention provides an anti-enzymatic antibacterial peptide I9H12 and a preparation method and application thereof. The sequence of antimicrobial peptide I9H12 is shown in SEQ ID No. 1 of the sequence listing. Preparation method: Referring to the properties of amino acids, while avoiding the cleavage sites of major proteases in the body as much as possible, the hydrophobic amino acid isoleucine (Ile) and the positively charged amino acid histidine (His) were selected as the main amino acids to design a new I9H12 antimicrobial peptide , and amidation of the carboxy terminus of the peptide to increase a positive charge and increase the stability of the peptide. Application of the antibacterial peptide in the preparation of targeted antibacterial drugs for treating Gram-negative bacteria or fungal infectious diseases. The invention effectively improves the anti-enzymatic hydrolysis ability of the antibacterial peptide and improves its application potential in actual production.

Description

technical field [0001] The invention belongs to the field of biotechnology, and in particular relates to an anti-enzymolysis antimicrobial peptide I9H12 and its preparation method and application. Background technique [0002] Antimicrobial peptides (AMPs) refer to a class of basic polypeptide substances with antibacterial activity induced in insects, which protect the body by inhibiting the growth of pathogens on the skin and mucosal surfaces of organisms. Many cells can release antimicrobial peptides, for example, epithelial cells, endothelial cells, leukocytes, platelets, etc. Antimicrobial peptides are usually composed of 12-50 amino acid residues, with a molecular weight of less than 10kDa. Most antimicrobial peptides contain positively charged amino acids, which are amphipathic and cationic. They are effective against a variety of bacteria, fungi, viruses, parasites and even cancers. Cells have inhibitory effect, and also have biological activities such as promoting w...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Patents(China)
IPC IPC(8): C07K14/00C07K1/04C07K1/06A61K38/16A61P31/10A61P31/04
Inventor 单安山来振衡邵长轩谭鹏朱永杰陈婷婷
Owner NORTHEAST AGRICULTURAL UNIVERSITY
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

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