综述

顶复门原虫蛋白质二硫键异构酶研究进展

  • 王璐阳 ,
  • 张乾 ,
  • 张素梅 ,
  • 张龙现
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  • 河南农业大学动物医学院,河南 郑州 450002
王璐阳(ORICD:0000-0002-6103-3821),男,博士研究生,从事人兽共患肠道原虫病入侵机制研究。 E-mail:wly952659965@foxmail.com
*张龙现(ORCID:0000-0001-9310-1975),男,博士,教授,从事人兽共患寄生虫病入侵机制及分子流行病学研究。E-mail:zhanglx8999@henau.edu.cn

收稿日期: 2024-12-25

  修回日期: 2025-02-10

  网络出版日期: 2025-05-27

基金资助

国家自然科学基金(32172882)

Progress of researches on the structure and biological functions of protein disulfide isomerase in apicomplexan protozoa

  • WANG Luyang ,
  • ZHANG Qian ,
  • ZHANG Sumei ,
  • ZHANG Longxian
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  • College of Veterinary Medicine, Henan Agricultural University, Zhengzhou 450002, Henan, China

Received date: 2024-12-25

  Revised date: 2025-02-10

  Online published: 2025-05-27

Supported by

National Natural Science Foundation of China(32172882)

摘要

顶复门原虫是一类专性细胞内寄生虫,多数为人兽共患病病原,其宿主范围广泛,可对畜牧养殖业造成巨大经济损失并严重威胁公共卫生安全。现有研究表明,蛋白质二硫键异构酶(PDI)广泛存在于顶复门原虫中,主要与寄生虫的入侵、黏附和细胞免疫有关,在寄生虫的生长发育过程中发挥重要的作用。本文对近年来已报道的顶复门原虫PDI的结构和生物学功能进行综述,以期为寄生虫病的防控和疫苗研发提供理论依据和新的策略。

本文引用格式

王璐阳 , 张乾 , 张素梅 , 张龙现 . 顶复门原虫蛋白质二硫键异构酶研究进展[J]. 中国寄生虫学与寄生虫病杂志, 2025 , 43(3) : 423 -428 . DOI: 10.12140/j.issn.1000-7423.2025.03.018

Abstract

Apicomplexan protozoa are a class of obligate intracellular parasites, and most of them are pathogens of zoonoses, with a wide range of hosts, causing huge economic losses to the livestock breeding industry and posing great threats to public health security. It has been demonstrated that protein disulfide isomerase (PDI) is widely present in apicomplexan protozoa, which is mainly associated with the invasion, adhesion and cellular immunity of parasites and plays an important role in the growth and development process of parasites. This review summarizes the advances in the structure and biological functions of PDI in apicomplexan protozoa, so as to provide insights into management of parasitic diseases and research and development of vaccines against parasitic diseases.

参考文献

[1] Hemphill A, Leitão A, Ortega-Mora LM, et al. Apico Wplexa 2022: 6th international meeting on apicomplexan parasites in farm animals[J]. Int J Parasitol, 2023, 53(9): 459-461.
[2] Rojas-Pirela M, Medina L, Rojas MV, et al. Congenital transmission of apicomplexan parasites: A review[J]. Front Microbiol, 2021, 12: 751648.
[3] Gui L, O’Shaughnessy WJ, Cai K, et al. Cryo-tomography reveals rigid-body motion and organization of apicomplexan invasion machinery[J]. Nat Commun, 2023, 14(1): 1775.
[4] Heintzelman MB. Gliding motility in apicomplexan parasites[J]. Semin Cell Dev Biol, 2015, 46: 135-142.
[5] Sibley LD. How apicomplexan parasites move in and out of cells[J]. Curr Opin Biotechnol, 2010, 21(5): 592-598.
[6] Wang L, Wang X, Wang CC. Protein disulfide-isomerase, a folding catalyst and a redox-regulated chaperone[J]. Free Radic Biol Med, 2015, 83: 305-313.
[7] Angrisano F, Ford A, Blagborough AM, et al. Protein disulfide isomerases: A way to tackle malaria[J]. Trends Parasitol, 2023, 39(8): 622-625.
[8] 梁程辉, 陈丹, 廖馨源, 等. 蛋白质二硫键异构酶的结构及抑制剂研究进展[J]. 生物化学与生物物理进展, 2020, 47(7): 595-606.
  Liang CH, Chen D, Liao XY, et al. Progress in the structural studies and inhibitor development of protein disulfide isomerase[J]. Prog Biochem Biophys, 2020, 47(7): 595-606. (in Chinese)
[9] Rahman NSA, Zahari S, Syafruddin SE, et al. Functions and mechanisms of protein disulfide isomerase family in cancer emergence[J]. Cell Biosci, 2022, 12(1): 129.
[10] 王志强, 周智敏, 郭占云. 蛋白质二硫键异构酶家族的结构与功能[J]. 生命科学研究, 2009, 13(6): 548-553.
  Wang ZQ, Zhou ZM, Guo ZY. The structure and function of the protein disulfide isomerase family[J]. Life Sci Res, 2009, 13(6): 548-553. (in Chinese)
[11] Tian G, Xiang S, Noiva R, et al. The crystal structure of yeast protein disulfide isomerase suggests cooperativity between its active sites[J]. Cell, 2006, 124(1): 61-73.
[12] Wang C, Li W, Ren JQ, et al. Structural insights into the redox-regulated dynamic conformations of human protein disulfide isomerase[J]. Antioxid Redox Signal, 2013, 19(1): 36-45.
[13] Lv KY, Chen S, Xu XL, et al. Protein disulfide isomerase cleaves allosteric disulfides in histidine-rich glycoprotein to regulate thrombosis[J]. Nat Commun, 2024, 15(1): 3129.
[14] Turano C, Coppari S, Altieri F, et al. Proteins of the PDI family: Unpredicted non-ER locations and functions[J]. J Cell Physiol, 2002, 193(2): 154-163.
[15] Parakh S, Atkin JD. Novel roles for protein disulphide isomerase in disease states: A double edged sword?[J]. Front Cell Dev Biol, 2015, 3: 30.
[16] Cai H, Wang CC, Tsou CL. Chaperone-like activity of protein disulfide isomerase in the refolding of a protein with no disulfide bonds[J]. J Biol Chem, 1994, 269(40): 24550-24552.
[17] Song JL, Wang CC. Chaperone-like activity of protein disulfide isomerase in the refolding of rhodanese[J]. Eur J Biochem, 1995, 231(2): 312-316.
[18] Winter J, Klappa P, Freedman RB, et al. Catalytic activity and chaperone function of human protein-disulfide isomerase are required for the efficient refolding of proinsulin[J]. J Biol Chem, 2002, 277(1): 310-317.
[19] Mahajan B, Noiva R, Yadava A, et al. Protein disulfide isomerase assisted protein folding in malaria parasites[J]. Int J Parasitol, 2006, 36(9): 1037-1048.
[20] Novo C, Martins TM, Prata S, et al. Gene sequencing, modelling and immunolocalization of the protein disulfide isomerase from Plasmodium chabaudi[J]. Int J Biol Macromol, 2009, 45(4): 399-406.
[21] Angrisano F, Sala KA, Tapanelli S, et al. Male-specific protein disulphide isomerase function is essential for Plasmodium transmission and a vulnerable target for intervention[J]. Sci Rep, 2019, 9(1): 18300.
[22] Mouray E, Moutiez M, Girault S, et al. Biochemical properties and cellular localization of Plasmodium falciparum protein disulfide isomerase[J]. Biochimie, 2007, 89(3): 337-346.
[23] Cobb DW, Kudyba HM, Villegas A, et al. A redox-active crosslinker reveals an essential and inhibitable oxidative folding network in the endoplasmic reticulum of malaria parasites[J]. PLoS Pathog, 2021, 17(2): e1009293.
[24] Angrisano F, Sala KA, Da DF, et al. Targeting the conserved fusion loop of HAP2 inhibits the transmission of Plasmodium berghei and falciparum[J]. Cell Rep, 2017, 21(10): 2868-2878.
[25] Zhang Y, Lai BS, Juhas M, et al. Toxoplasma gondii secretory proteins and their role in invasion and pathogenesis[J]. Microbiol Res, 2019, 227: 126293.
[26] DeRocher AE, Coppens I, Karnataki A, et al. A thioredoxin family protein of the apicoplast periphery identifies abundant candidate transport vesicles in Toxoplasma gondii[J]. Eukaryot Cell, 2008, 7(9): 1518-1529.
[27] Biddau M, Bouchut A, Major J, et al. Two essential thioredoxins mediate apicoplast biogenesis, protein import, and gene expression in Toxoplasma gondii[J]. PLoS Pathog, 2018, 14(2): e1006836.
[28] Zhang ZW, Li TT, Wang JL, et al. Functional characterization of two thioredoxin proteins of Toxoplasma gondii using the CRISPR-Cas9 system[J]. Front Vet Sci, 2021, 7: 614759.
[29] Zhang ZW, Wang M, Sun LX, et al. Trx4, a novel thioredoxin protein, is important for Toxoplasma gondii fitness[J]. Parasit Vectors, 2024, 17(1): 178.
[30] Moncada D, Arenas A, Acosta A, et al. Role of the 52 KDa thioredoxin protein disulfide isomerase of Toxoplasma gondii during infection to human cells[J]. Exp Parasitol, 2016, 164: 36-42.
[31] Wang HL, Li YQ, Yin LT, et al. Toxoplasma gondii protein disulfide isomerase (TgPDI) is a novel vaccine candidate against toxoplasmosis[J]. PLoS One, 2013, 8(8): e70884.
[32] 王海龙, 李润花, 殷丽天, 等. 刚地弓形虫蛋白质二硫键异构酶基因的克隆及原核表达[J]. 环境与健康杂志, 2013, 30(10): 875-878.
  Wang HL, Li RH, Yin LT, et al. Gene-cloning, prokaryotic expression and immunoreactivity analysis of protein disulfide isomerase in Toxoplasma gondii[J]. J Environ Health, 2013, 30(10): 875-878. (in Chinese)
[33] 王宁, 薛俊欣, 丁佳乐, 等. 弓形虫蛋白质二硫键异构酶的免疫保护作用[J]. 中国兽医学报, 2019, 39(6): 1157-1162.
  Wang N, Xue JX, Ding JL, et al. Immumological protection effects of Toxoplasma gondii protein disulfide isomerase[J]. Chin J Vet Sci, 2019, 39(6): 1157-1162. (in Chinese)
[34] Meek B, Back JW, Klaren VNA, et al. Protein disulfide isomerase of Toxoplasma gondii is targeted by mucosal IgA antibodies in humans[J]. FEBS Lett, 2002, 522(1/2/3): 104-108.
[35] Wang CY, Sun P, Jia YG, et al. Protein disulfide isomerase PDI8 is indispensable for parasite growth and associated with secretory protein processing in Toxoplasma gondii[J]. mBio, 2024, 15(9): e0205124.
[36] Blunt DS, Montelone BA, Upton SJ, et al. Sequence of the parasitic protozoan, Cryptosporidium parvum, putative protein disulfide isomerase-encoding DNA[J]. Gene, 1996, 181(1/2): 221-223.
[37] Snelling WJ, Lin QS, Moore JE, et al. Proteomics analysis and protein expression during sporozoite excystation of Cryptosporidium parvum (Coccidia, apicomplexa)[J]. Mol Cell Proteom, 2007, 6(2): 346-355.
[38] Mauzy MJ, Enomoto S, Lancto CA, et al. The Cryptosporidium parvum transcriptome during in vitro development[J]. PLoS One, 2012, 7(3): e31715.
[39] Naguleswaran A, Alaeddine F, Guionaud C, et al. Neospora caninum protein disulfide isomerase is involved in tachyzoite-host cell interaction[J]. Int J Parasitol, 2005, 35(13): 1459-1472.
[40] Han HY, Dong H, Zhu SH, et al. Molecular characterization and analysis of a novel protein disulfide isomerase-like protein of Eimeria tenella[J]. PLoS One, 2014, 9(6): e99914.
[41] Jalovecka M, Sojka D, Ascencio M, et al. Babesia life cycle-when phylogeny meets biology[J]. Trends Parasitol, 2019, 35(5): 356-368.
[42] Ikadai H, Tsukada R, Sasaki M, et al. Molecular characterization of a putative protein disulfide isomerase from Babesia caballi[J]. Parasitology, 2005, 131(Pt 6): 775-782.
[43] Padilla A, Noiva R, Lee N, et al. An atypical protein disulfide isomerase from the protozoan parasite Leishmania containing a single thioredoxin-like domain[J]. J Biol Chem, 2003, 278(3): 1872-1878.
[44] Ben Khalaf N, De Muylder G, Louzir H, et al. Leishmania major protein disulfide isomerase as a drug target: Enzymatic and functional characterization[J]. Parasitol Res, 2012, 110(5): 1911-1917.
[45] Ben Achour Y, Chenik M, Louzir H, et al. Identification of a disulfide isomerase protein of Leishmania major as a putative virulence factor[J]. Infect Immun, 2002, 70(7): 3576-3585.
[46] Ben Khalaf N, Pham S, Romeo G, et al. A computer-aided approach to identify novel Leishmania major protein disulfide isomerase inhibitors for treatment of leishmaniasis[J]. J Comput Aided Mol Des, 2021, 35(3): 297-314.
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