Phrixotoxin (PaTx-1) and application thereof

A 1.patx-1, toxin technology, applied in the direction of medical preparations containing active ingredients, antibody mimics/scaffolds, depsipeptides, etc., can solve the problems of side effects, low efficacy, low safety and so on

Active Publication Date: 2019-02-22
广东帕派恩生物科技有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0007] Currently used sodium channel blockers, such as carbamazepine, lidocaine, and the above-mentioned polypeptide toxins, have multiple types of non-selective effects on sodium channels, which easily cause central and circulatory side effects (such as dizziness, ataxia, insomnia, nausea and headache, etc.), or have defects of low effectiveness and low safety, thus limiting their clinical application and widespread use

Method used

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  • Phrixotoxin (PaTx-1) and application thereof
  • Phrixotoxin (PaTx-1) and application thereof
  • Phrixotoxin (PaTx-1) and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0054] The amino acid sequence of the PaTx-1 polypeptide toxin in this example is shown in Table 1 below.

[0055] Table 1

[0056]

[0057] Remarks: The W amino acid at the end of SEQ ID NO: 4 and SEQ ID NO: 6 to SEQ ID NO: 19 has been aminated, that is, an amino group has been added.

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PUM

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Abstract

The invention mainly relates to phrixotoxin (PaTx-1) extended polypeptide and application thereof. The polypeptide toxin can effectively and selectively block Nav1.7 (voltage-gated sodium channel alpha subunit group), and therefore the polypeptide toxin can serve as a selective sodium ion channel blocking agent so as to be applied to multiple aspects such as molecular mechanisms, neutral signal transmission and disease treatment relevant to Nav1.7 sodium ion channels.

Description

technical field [0001] The present invention relates to a polypeptide substance and its use in medicine preparation, in particular to a polypeptide toxin capable of effectively and selectively blocking Nav1.7 (a voltage-gated sodium channel α subunit family) and its use. Background technique [0002] Voltage-gated sodium channels (VGSCs) are widely distributed and expressed in various tissues of both vertebrates and invertebrates. VGSCs play an important role in the generation and burst of action potentials and in the transmission of nerve signals. Many diseases are closely related to voltage-gated sodium ion channels, such as pain, epilepsy and so on. [0003] VGSCs are high molecular weight, multi-transmembrane glycoproteins on excitatory cell membranes. In 2003, the International Pharmacological Federation announced the nomenclature of VGSCs. The English abbreviation (NaV) means a voltage-sensitive sodium ion channel, where Na stands for a sodium ion channel, and V sta...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C07K14/00A61K38/16C07K19/00A61P29/00C12N15/11
CPCA61K38/00A61P29/00C07K14/00C07K2319/00
Inventor 潘伟飚
Owner 广东帕派恩生物科技有限公司
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