• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

红细胞膜蛋白参与对疟原虫和疟原虫感染的免疫反应。

Erythrocyte membrane proteins involved in the immune response to Plasmodium falciparum and Plasmodium vivax infection.

机构信息

Biochemistry and Diseases Research Group, Facultad de Medicina, Universidad de Cartagena, Cartagena, 130015, Colombia.

Grupo de Investigaciones Biomédicas-GIB, Universidad de San Buenaventura, Cartagena, 130010, Colombia.

出版信息

Parasitol Res. 2021 May;120(5):1789-1797. doi: 10.1007/s00436-021-07135-6. Epub 2021 Apr 2.

DOI:10.1007/s00436-021-07135-6
PMID:33797613
Abstract

Invasion of Plasmodium into the red blood cell involves the interactions of a substantial number of proteins, with red cell membrane proteins as the most involved throughout the process from entry to exit. The objective of this work was to identify proteins of the human erythrocyte membrane capable of generating an antigenic response to P. falciparum and P. vivax infection, with the goal of searching for new molecular targets of interest with an immunological origin to prevent Plasmodium infection. To identify these proteins, an immunoproteomic technique was carried out in four stages: protein separation (electrophoresis), detection of antigenic proteins (western blotting), identification of proteins of interest (mass spectrometry), and interpretation of the data (bioinformatic analysis). Four proteins were identified from extracts of membrane proteins from erythrocytes infected with P. falciparum: Spectrin, Ankyrin-1, Band 3 and band 4.2, and a single protein was identified from erythrocytes infected with P. vivax: Band 3. These results demonstrate that modifications in the red blood cell membrane during infection with P. falciparum and P. vivax can generate an immune response, altering proteins of great structural and functional importance.

摘要

疟原虫侵入红细胞涉及大量蛋白质的相互作用,在从进入到退出的整个过程中,红细胞膜蛋白的参与最多。这项工作的目的是鉴定能够对恶性疟原虫和间日疟原虫感染产生抗原反应的人红细胞膜蛋白,以寻找具有免疫起源的新的、感兴趣的分子靶标来预防疟原虫感染。为了鉴定这些蛋白质,我们在四个阶段进行了免疫蛋白质组学技术:蛋白质分离(电泳)、抗原蛋白检测(western blot)、感兴趣蛋白鉴定(质谱)和数据解释(生物信息学分析)。从感染恶性疟原虫和间日疟原虫的红细胞膜蛋白提取物中鉴定出 4 种蛋白:血影蛋白、锚蛋白-1、带 3 和带 4.2,从感染间日疟原虫的红细胞中鉴定出 1 种蛋白:带 3。这些结果表明,恶性疟原虫和间日疟原虫感染期间红细胞膜的改变可以产生免疫反应,改变具有重要结构和功能的蛋白质。

相似文献

1
Erythrocyte membrane proteins involved in the immune response to Plasmodium falciparum and Plasmodium vivax infection.红细胞膜蛋白参与对疟原虫和疟原虫感染的免疫反应。
Parasitol Res. 2021 May;120(5):1789-1797. doi: 10.1007/s00436-021-07135-6. Epub 2021 Apr 2.
2
A novel in vitro model reveals distinctive modulatory roles of Plasmodium falciparum and Plasmodium vivax on naïve cell-mediated immunity.一种新型体外模型揭示了恶性疟原虫和间日疟原虫对天然细胞介导免疫的独特调节作用。
Malar J. 2017 Mar 27;16(1):131. doi: 10.1186/s12936-017-1781-4.
3
Differential cellular recognition of antigens during acute Plasmodium falciparum and Plasmodium vivax malaria.急性间日疟原虫和恶性疟原虫感染时抗原的细胞差异识别。
J Infect Dis. 2011 Apr 15;203(8):1192-1199. doi: 10.1093/infdis/jiq166.
4
Plasmodium vivax but Not Plasmodium falciparum Blood-Stage Infection in Humans Is Associated with the Expansion of a CD8+ T Cell Population with Cytotoxic Potential.间日疟原虫而非恶性疟原虫在人体中的血液阶段感染与具有细胞毒性潜能的CD8 + T细胞群体的扩增有关。
PLoS Negl Trop Dis. 2016 Dec 8;10(12):e0005031. doi: 10.1371/journal.pntd.0005031. eCollection 2016 Dec.
5
Life-spans of human T-cell responses to determinants from the circumsporozoite proteins of Plasmodium falciparum and Plasmodium vivax.人类对恶性疟原虫和间日疟原虫环子孢子蛋白决定簇的T细胞反应的寿命。
Proc Natl Acad Sci U S A. 1994 Jun 21;91(13):6118-22. doi: 10.1073/pnas.91.13.6118.
6
Characterization of peripheral blood lymphocyte subsets in patients with acute Plasmodium falciparum and P. vivax malaria infections at Wonji Sugar Estate, Ethiopia.埃塞俄比亚翁吉糖厂急性恶性疟原虫和间日疟原虫疟疾感染患者外周血淋巴细胞亚群的特征分析
Clin Vaccine Immunol. 2006 Mar;13(3):376-9. doi: 10.1128/CVI.13.3.376-379.2006.
7
Cross-Species Immune Recognition Between Plasmodium vivax Duffy Binding Protein Antibodies and the Plasmodium falciparum Surface Antigen VAR2CSA.间日疟原虫 Duffy 结合蛋白抗体与恶性疟原虫表面抗原 VAR2CSA 的种间免疫识别。
J Infect Dis. 2019 Jan 1;219(1):110-120. doi: 10.1093/infdis/jiy467.
8
Acquired immunity in a holoendemic setting of Plasmodium falciparum and p. Vivax malaria.在恶性疟原虫和间日疟原虫疟疾高度流行环境中的获得性免疫。
Am J Trop Med Hyg. 2007 Jun;76(6):995-6.
9
Functional antibodies against VAR2CSA in nonpregnant populations from colombia exposed to Plasmodium falciparum and Plasmodium vivax.哥伦比亚无妊娠人群中针对恶性疟原虫和间日疟原虫的功能性 VAR2CSA 抗体。
Infect Immun. 2014 Jun;82(6):2565-73. doi: 10.1128/IAI.01594-14. Epub 2014 Mar 31.
10
Cross-reactive anti-PfCLAG9 antibodies in the sera of asymptomatic parasite carriers of Plasmodium vivax.间日疟原虫无症状带虫者血清中交叉反应性抗 PfCLAG9 抗体。
Mem Inst Oswaldo Cruz. 2013 Feb;108(1):98-105. doi: 10.1590/s0074-02762013000100016.

引用本文的文献

1
Plasmodium vivax tryptophan-rich antigen reduces type I collagen secretion via the NF-κBp65 pathway in splenic fibroblasts.恶性疟原虫色氨酸丰富抗原通过 NF-κBp65 通路减少脾成纤维细胞 I 型胶原分泌。
Parasit Vectors. 2024 May 27;17(1):239. doi: 10.1186/s13071-024-06264-y.
2
Identification and subcellular localization analysis of membrane protein Ycf 1 in the microsporidian .鉴定微孢子虫中的膜蛋白 Ycf1 及其亚细胞定位分析
PeerJ. 2022 Jul 8;10:e13530. doi: 10.7717/peerj.13530. eCollection 2022.
3
Protein PvTRAg23 Triggers Spleen Fibroblasts for Inflammatory Profile and Reduces Type I Collagen Secretion NF-κBp65 Pathway.

本文引用的文献

1
Biomarkers of disease severity in vivax malaria.间日疟疾病严重程度的生物标志物。
Parasitol Res. 2021 Apr;120(4):1437-1446. doi: 10.1007/s00436-021-07065-3. Epub 2021 Feb 3.
2
Autoimmune Anemia in Malaria.疟疾相关性自身免疫性溶血性贫血。
Trends Parasitol. 2020 Feb;36(2):91-97. doi: 10.1016/j.pt.2019.12.002. Epub 2019 Dec 18.
3
Oxidative Stress Enhances Dendritic Cell Responses to .氧化应激增强树突状细胞对……的反应 。 (原文结尾不完整)
蛋白 PvTRAg23 触发脾脏成纤维细胞炎症表型,减少 I 型胶原分泌 NF-κBp65 通路。
Front Immunol. 2022 Jun 13;13:877122. doi: 10.3389/fimmu.2022.877122. eCollection 2022.
Immunohorizons. 2019 Nov 5;3(11):511-518. doi: 10.4049/immunohorizons.1900076.
4
Membrane protein carbonylation of Plasmodium falciparum infected erythrocytes under conditions of sickle cell trait and G6PD deficiency.镰状细胞性状和葡萄糖-6-磷酸脱氢酶缺乏条件下恶性疟原虫感染红细胞的膜蛋白羰基化
Mol Biochem Parasitol. 2019 Jan;227:5-14. doi: 10.1016/j.molbiopara.2018.11.003. Epub 2018 Nov 22.
5
Plasmodium genomics: an approach for learning about and ending human malaria.疟原虫基因组学:一种了解并终结人类疟疾的方法。
Parasitol Res. 2019 Jan;118(1):1-27. doi: 10.1007/s00436-018-6127-9. Epub 2018 Nov 6.
6
Anti-band 3 and anti-spectrin antibodies are increased in Plasmodium vivax infection and are associated with anemia.抗带 3 抗体和抗血影蛋白抗体在间日疟原虫感染中增加,并与贫血有关。
Sci Rep. 2018 Jun 8;8(1):8762. doi: 10.1038/s41598-018-27109-6.
7
Transitional B Cells and TLR9 Responses Are Defective in Selective IgA Deficiency.选择性 IgA 缺陷症中过渡 B 细胞和 TLR9 反应存在缺陷。
Front Immunol. 2018 Apr 27;9:909. doi: 10.3389/fimmu.2018.00909. eCollection 2018.
8
Malaria.疟疾。
Lancet. 2018 Apr 21;391(10130):1608-1621. doi: 10.1016/S0140-6736(18)30324-6. Epub 2018 Apr 6.
9
Mechanisms of naturally acquired immunity to P. falciparum and approaches to identify merozoite antigen targets.对恶性疟原虫自然获得性免疫的机制及鉴定裂殖子抗原靶点的方法
Parasitology. 2018 Jun;145(7):839-847. doi: 10.1017/S0031182017001949. Epub 2017 Nov 16.
10
Plasmodium DNA-mediated TLR9 activation of T-bet B cells contributes to autoimmune anaemia during malaria.疟原虫 DNA 介导的 TLR9 激活 T-bet 细胞有助于疟疾期间的自身免疫性贫血。
Nat Commun. 2017 Nov 3;8(1):1282. doi: 10.1038/s41467-017-01476-6.