α-conotoxin peptide txic/txd1, its pharmaceutical composition and use
A technology of use and medicine, applied in the fields of biochemistry and molecular biology, can solve problems such as addiction and cardiac side effects
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Embodiment 1
[0099] Example 1: Gene cloning and sequence analysis of α-conotoxin TxIC / Txd1
[0100] 1. Extraction of Genomic DNA from Cono venom glands
[0101] Live brocade snails (C.textile Linnaeus) collected from the coasts of Hainan Island and Xisha Islands were used as materials, and stored at -80°C for later use. Cono venom glands were first dissected out and weighed. Then, the genomic DNA of the poisonous glands was extracted with a marine animal genomic DNA extraction kit (purchased from Beijing Tiangen Biochemical Technology Co., Ltd., China), and the specific operation was performed according to the kit instructions. Genomic DNA of venom glands was obtained.
[0102] Dissolve the extracted venom gland genomic DNA in 100 μL TE, take 5 μL for 1.0% agarose gel electrophoresis, and use λ-EcoT14 I digest DNA Marker as a standard to detect the integrity and size of the obtained DNA. Determination of OD of DNA solution with a nucleic acid protein analyzer 260 、OD 280 value and OD ...
Embodiment 2
[0136] Embodiment 2: the artificial synthesis of α-conotoxin TxIC
[0137] According to the amino acid sequence of the α-conotoxin TxIC mature peptide (SEQ ID NO: 7, C-terminal amidation), the TxIC linear peptide was artificially synthesized by the Fmoc method ( Figure 2A ). The specific method is as follows:
[0138]The resin peptide is artificially synthesized by Fmoc chemical method, and the resin peptide can be synthesized by a peptide synthesizer or manual synthesis. Except for cysteine, the remaining amino acids use standard side chain protecting groups. The -SH of the 1st and 3rd cysteine (Cys) of TxIC is protected with Trt (S-trityl), and the -SH of the 2nd and 4th cysteine is protected with Acm (S-acetamidomethyl) pairwise . The synthesis steps are as follows: using the Fmoc and FastMoc methods in the solid-phase synthesis method, three isomeric linear peptides were synthesized on an ABI Prism 433a peptide synthesizer. The side chain protecting groups of F...
Embodiment 3
[0142] Example 3: Experiment of α-conotoxin TxIC specifically blocking α3β4nAChR
[0143] Reference literature (Azam L, Yoshikami D, McIntosh JM.Amino acid residues that confer high selectivity of the alpha6 nicotinic acetylcholine receptor subunit to alpha-conotoxinMII[S4A,E11A,L15A].J Biol Chem.2008;283(17):11625-32 .) and the instructions of mMessage mMachine in vitro transcription kit (Ambion, Austin, TX) to prepare various rat neurotype nAChRs subtypes (α3β4, α6 / α3β4, α9α10, α4β2, α4β4 , α3β4, α2β2, α2β4, α7), human α3β4, and mouse muscle nAChRs (α1β1δε) cRNA, the concentration was measured by OD value under UV 260nm. Xenopus laveis oocytes (frog eggs) were collected by dissection, and cRNA was injected into the frog eggs, and the injection amount of each subunit was 5ng cRNA. Each subunit of muscle nAChR was injected with 0.5-2.5ng DNA. Frog eggs were cultured in ND-96. cRNA was injected within 1-2 days after frog egg collection, and used for voltage-clamp recording...
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