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

Sea anemone neurotoxin gene Sr3 and application thereof

A technology of neurotoxin and sea anemone, which is applied in application, genetic engineering, plant genetic improvement, etc., can solve the problem of less neurotoxin in sea anemone, and achieve the effect of prolonging the effective refractory period and enhancing atrial contraction

Inactive Publication Date: 2006-06-14
SUN YAT SEN UNIV
View PDF0 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

At present, there are few domestic research reports on sea anemone neurotoxins

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
  • Sea anemone neurotoxin gene Sr3 and application thereof
  • Sea anemone neurotoxin gene Sr3 and application thereof
  • Sea anemone neurotoxin gene Sr3 and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0028] Example 1: Extraction and RT-PCR amplification of total RNA from tentacles of rose red and green sea anemone

[0029]Extraction of total RNA and synthesis of cDNA: Isolate the tentacles of the rose red and green sea anemone, extract the total RNA of the tentacles by the guanidine isothiocyanate method, and remove the protein by phenol / chloroform extraction. Obtain 100 μg of the total RNA of the venomous glands, and its A 260 / A 280 = 2.03, two clear bands of 18s and 28s were detected by 1% formaldehyde denaturing gel electrophoresis, and the ratio was >1 (see Figure 2), indicating that the integrity of the total RNA was good.

[0030] Take 1ug of total RNA with SMART III olignuclotide (5'-AAGCAGTGGTATCAACGCAGAGTGGCCATTATGGCCGGG-3') and CDSIII / 3'PCR primer (5'-ATTCTAGAGGCCGAGGCGGCCGACATG-d(T) 30 N -1 N-3′) was reverse transcribed to synthesize the first strand to obtain 10 μl of cDNA first strand product.

[0031] Primer design and RT-PCR amplification: According to t...

Embodiment 2

[0036] Example 2: Determination and analysis of recombinant sea anemone neurotoxin gene sequence

[0037] The recovered electrophoresis product was connected to the T vector, transformed into DH5α Escherichia coli, and the recombinant clones were selected for sequencing. A total of 25 clones were determined, and Blast homology analysis showed that these 25 clones were all neurotoxin gene sequences, and the gene length was 141bp. Each encodes 47 amino acid toxin proteins, one of which is numbered Sr-p3, which is not completely identical to the amino acid sequence of the reported sea anemone neurotoxin protein, and is a new toxin protein.

[0038] At present, there are more than 20 kinds of sea anemone neurotoxins reported, the number of amino acids is between 46-49 (in addition, there are several toxins with amino acid residues between 27-31, called short-chain neurotoxins), of which 12 amino acids are conserved .According to their amino acid sequences, they can be divided into...

Embodiment 3

[0041] Example 3: Construction of recombinant sea anemone neurotoxin expression plasmid

[0042] A pair of primers were synthesized according to the sequences at both ends of the Sr3 gene, the upstream primers contained Kpn I and Prescission Protease cleavage sites, and the downstream primers contained BamH I cleavage sites.

[0043] Upstream primer (B1): 5'CGG GGT ACC CTG GAA GTT CTG TTC CAG GGG CCC GGG GTG

[0044] Kpn I Precision Protease site

[0045] CCATGC CTG TGC GAC 3';

[0046] Downstream primer (B2): 5'CGC GGA TCC TTA TTA CTT TIT GCA GCA CCA GCC AAT G3';

[0047] Bam H I

[0048] The pGEM-TEasy plasmid (purchased from Promega) containing the Sr3 gene was used as a template, and B1 and B2 were used as primers for PCR amplification to obtain a specifically amplified single band with a product size of about 200 bp. The PCR amplification product was first cloned into the BSK plasmid with the combination of K...

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

PropertyMeasurementUnit
molecular weightaaaaaaaaaa
molecular weightaaaaaaaaaa
Login to View More

Abstract

The invention relates to a sea anemone neurotoxin gene Sr3 and its coded protein, as well as the application of the protein in the preparation of drugs for treating cardiovascular diseases. The present invention uses the method of RT-PCR to isolate and obtain from the total RNA of the tentacle of the rose red and green sea anemone

Description

technical field [0001] The invention relates to a sea anemone neurotoxin gene Sr3 and its coded protein, as well as the application of the protein in the preparation of drugs for treating cardiovascular diseases. Background technique [0002] Sea anemone (anthopleura), belonging to coelenterate (soelenterata), coral class (anthozoa), is a relatively primitive animal in the ocean. In the long-term biological evolution process, in order to resist predators and capture food, the nematocysts of sea anemone tentacles can secrete a variety of sea anemone toxins, basically polypeptide toxins, which have various physiological activities on humans and animals. Sea anemone toxins are divided into three categories according to their physiological functions: sea anemone neurotoxins, sea anemone cytolysins, and sea anemone potassium channel inhibitors. [0003] Foreign studies on sea anemone neurotoxins began in the 1970s. In 1976, Shibata and others from the University of Hawaii in th...

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): C12N15/30C12N15/10C07K14/44C07K19/00C12P19/34C12N15/70A61K38/17A61P9/00
Inventor 徐安龙陈慧萍王磊董美玲杨文利姜孝玉涂洪斌
Owner SUN YAT SEN UNIV
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