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重组PDIA3蛋白的制备、活性测定及小分子抑制剂筛选

龙丹杰 雷成寿 王宗华 林琳

福建农业科技2026,Vol.57Issue(1):8-14,7.
福建农业科技2026,Vol.57Issue(1):8-14,7.DOI:10.13651/j.cnki.fjnykj.2026.01.002

重组PDIA3蛋白的制备、活性测定及小分子抑制剂筛选

Preparation,Activity Determination of Recombinant PDIA3 Protein and Screening for Its Small-molecule Inhibitors

龙丹杰 1雷成寿 1王宗华 2林琳3

作者信息

  • 1. 福建农林大学生命科学学院,福建 福州 350002||闽江学院材料与化学工程学院,福建 福州 350108
  • 2. 福建农林大学生命科学学院,福建 福州 350002||福州海洋研究院,福建 福州 350108
  • 3. 闽江学院材料与化学工程学院,福建 福州 350108||福州海洋研究院,福建 福州 350108
  • 折叠

摘要

Abstract

Protein disulfide-isomerase A3(PDIA3),a member of the PDI family,plays a core role in regulating the formation,cleavage,and rearrangement of protein disulfide bonds.This enzyme is closely associated with the occurrence and progression of various physiological and pathological processes,including thrombosis,cancer,neurodegenerative diseases,and viral infections,making it a highly promising target for drug intervention.In this study,the gene encoding PDIA3 was introduced into an Escherichia coli expression system,and recombinant PDIA3 protein with biological activity was successfully expressed and purified.Based on the establishment of a high-throughput screening method for PDIA3 inhibitors,110 small-molecule inhibitors of PDIA3 were identified from a natural product library comprising 4,080 compounds.Among these,Punicalagin,a major polyphenolic compound found in pomegranate peel,exhibited a relatively significant inhibitory effect,with a half-maximal inhibitory concentration(IC50)of 2.3 μmol·L-1.Molecular docking results suggested that Punicalagin may bind to the b'domain of PDIA3.This study provides candidate molecules and a theoretical basis for the development of PDIA3-targeted drugs.

关键词

PDIA3蛋白/抑制剂/高通量筛选/分子对接

Key words

PDIA3 protein/Inhibitor/High-throughput screening/Molecular docking

分类

化学化工

引用本文复制引用

龙丹杰,雷成寿,王宗华,林琳..重组PDIA3蛋白的制备、活性测定及小分子抑制剂筛选[J].福建农业科技,2026,57(1):8-14,7.

基金项目

福建省自然科学基金重点项目(2022J02052) (2022J02052)

福州海洋研究院项目(2022F15). (2022F15)

福建农业科技

0253-2301

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