• 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

基因破坏揭示了伯氏疟原虫生命周期中组织蛋白酶七的非必需作用。

Gene disruption reveals a dispensable role for plasmepsin VII in the Plasmodium berghei life cycle.

作者信息

Mastan Babu S, Kumari Anchala, Gupta Dinesh, Mishra Satish, Kumar Kota Arun

机构信息

Department of Animal Sciences, School of Life Sciences, University of Hyderabad, Hyderabad, India.

Bioinformatics Laboratory, SCB Group, International Centre for Genetic Engineering and Biotechnology, Aruna Asaf Ali Marg, 110 067 New Delhi, India.

出版信息

Mol Biochem Parasitol. 2014 Jun;195(1):10-3. doi: 10.1016/j.molbiopara.2014.05.004. Epub 2014 Jun 2.

DOI:10.1016/j.molbiopara.2014.05.004
PMID:24893340
Abstract

Plasmepsins (PM), aspartic proteases of Plasmodium, comprises a family of ten proteins that perform critical functions in Plasmodium life cycle. Except VII and VIII, functions of the remaining plasmepsin members have been well characterized. Here, we have generated a mutant parasite lacking PM VII in Plasmodium berghei using reverse genetics approach. Systematic comparison of growth kinetics and infection in both mosquito and vertebrate host revealed that PM VII depleted mutants exhibited no defects in development and progressed normally throughout the parasite life cycle. These studies suggest a dispensable role for PM VII in Plasmodium berghei life cycle.

摘要

疟原虫天冬氨酸蛋白酶(PM)是疟原虫的天冬氨酸蛋白酶,由十种蛋白质组成的家族,它们在疟原虫生命周期中发挥关键作用。除了VII和VIII之外,其余疟原虫天冬氨酸蛋白酶成员的功能已得到充分表征。在这里,我们使用反向遗传学方法在伯氏疟原虫中产生了一种缺乏PM VII的突变寄生虫。对蚊子和脊椎动物宿主中的生长动力学和感染进行系统比较后发现,缺乏PM VII的突变体在发育过程中没有缺陷,并且在整个寄生虫生命周期中正常发育。这些研究表明PM VII在伯氏疟原虫生命周期中作用不大。

相似文献

1
Gene disruption reveals a dispensable role for plasmepsin VII in the Plasmodium berghei life cycle.基因破坏揭示了伯氏疟原虫生命周期中组织蛋白酶七的非必需作用。
Mol Biochem Parasitol. 2014 Jun;195(1):10-3. doi: 10.1016/j.molbiopara.2014.05.004. Epub 2014 Jun 2.
2
Plasmodium berghei plasmepsin VIII is essential for sporozoite gliding motility.伯氏疟原虫天冬氨酸蛋白酶VIII对子孢子滑行运动至关重要。
Int J Parasitol. 2017 Apr;47(5):239-245. doi: 10.1016/j.ijpara.2016.11.009. Epub 2017 Feb 10.
3
Protein -Fucosyltransferase 2 Is Not Essential for Development.蛋白岩藻糖基转移酶 2 对于发育并非必需。
Front Cell Infect Microbiol. 2019 Jul 3;9:238. doi: 10.3389/fcimb.2019.00238. eCollection 2019.
4
Plasmodium Cysteine Repeat Modular Proteins 3 and 4 are essential for malaria parasite transmission from the mosquito to the host.疟原虫半胱氨酸重复模块蛋白 3 和 4 对于疟原虫从蚊子到宿主的传播是必需的。
Malar J. 2011 Mar 31;10:71. doi: 10.1186/1475-2875-10-71.
5
Plasmodium falciparum ookinete expression of plasmepsin VII and plasmepsin X.恶性疟原虫动合子中组织蛋白酶VII和组织蛋白酶X的表达
Malar J. 2016 Feb 24;15:111. doi: 10.1186/s12936-016-1161-5.
6
ADF2 is required for transformation of the ookinete and sporozoite in malaria parasite development.ADF2 在疟原虫发育过程中的卵囊和子孢子转化中是必需的。
Biochem Biophys Res Commun. 2010 Jul 9;397(4):668-72. doi: 10.1016/j.bbrc.2010.05.155. Epub 2010 Jun 8.
7
Disruption of the Plasmodium berghei 2-Cys peroxiredoxin TPx-1 gene hinders the sporozoite development in the vector mosquito.伯氏疟原虫2-半胱氨酸过氧化物酶TPx-1基因的破坏阻碍了媒介蚊子中子孢子的发育。
Mol Biochem Parasitol. 2008 Jun;159(2):142-5. doi: 10.1016/j.molbiopara.2008.03.002. Epub 2008 Mar 13.
8
Enzymatic Characterization of Recombinant Food Vacuole Plasmepsin 4 from the Rodent Malaria Parasite Plasmodium berghei.来自啮齿动物疟原虫伯氏疟原虫的重组食物泡组织蛋白酶4的酶学特性分析
PLoS One. 2015 Oct 28;10(10):e0141758. doi: 10.1371/journal.pone.0141758. eCollection 2015.
9
The Plasmodium protein P113 supports efficient sporozoite to liver stage conversion in vivo.疟原虫蛋白P113在体内支持子孢子高效转化为肝期。
Mol Biochem Parasitol. 2014 Feb;193(2):101-9. doi: 10.1016/j.molbiopara.2014.03.002. Epub 2014 Mar 20.
10
Depletion of the Plasmodium berghei thrombospondin-related sporozoite protein reveals a role in host cell entry by sporozoites.去除伯氏疟原虫血小板反应蛋白相关子孢子蛋白揭示其在子孢子进入宿主细胞中的作用。
Mol Biochem Parasitol. 2007 Jun;153(2):158-66. doi: 10.1016/j.molbiopara.2007.03.001. Epub 2007 Mar 6.

引用本文的文献

1
Structure-activity analysis of imino-pyrimidinone-fused pyrrolidines aids the development of dual plasmepsin V and plasmepsin X inhibitors.亚氨基嘧啶酮稠合吡咯烷的构效关系分析有助于双血浆蛋白酶V和血浆蛋白酶X抑制剂的开发。
FEBS J. 2025 Jun;292(11):2843-2864. doi: 10.1111/febs.70038. Epub 2025 Mar 4.
2
Malaria parasite cysteine and aspartic proteases as key drug targets for antimalarial therapy.疟原虫半胱氨酸和天冬氨酸蛋白酶作为抗疟治疗的关键药物靶点。
J Mol Model. 2025 Feb 8;31(3):78. doi: 10.1007/s00894-025-06303-0.
3
Plasmepsin-like Aspartyl Proteases in .
疟原虫中的类组织蛋白酶D天冬氨酸蛋白酶
Pathogens. 2021 Sep 26;10(10):1241. doi: 10.3390/pathogens10101241.
4
Malaria parasite plasmepsins: More than just plain old degradative pepsins.疟原虫原浆朊酶:不只是普通的古老降解胃蛋白酶。
J Biol Chem. 2020 Jun 19;295(25):8425-8441. doi: 10.1074/jbc.REV120.009309. Epub 2020 May 4.
5
Deciphering the mechanism of potent peptidomimetic inhibitors targeting plasmepsins - biochemical and structural insights.解析针对质体朊酶的强效肽模拟抑制剂的作用机制——生化和结构见解。
FEBS J. 2018 Aug;285(16):3077-3096. doi: 10.1111/febs.14598. Epub 2018 Jul 7.
6
Proteases as antimalarial targets: strategies for genetic, chemical, and therapeutic validation.蛋白酶作为抗疟靶点:遗传、化学和治疗验证策略。
FEBS J. 2017 Aug;284(16):2604-2628. doi: 10.1111/febs.14130. Epub 2017 Jul 3.
7
Altered Plasmodium falciparum Sensitivity to the Antiretroviral Protease Inhibitor Lopinavir Associated with Polymorphisms in pfmdr1.恶性疟原虫对抗逆转录病毒蛋白酶抑制剂洛匹那韦的敏感性改变与pfmdr1基因多态性相关。
Antimicrob Agents Chemother. 2016 Dec 27;61(1). doi: 10.1128/AAC.01949-16. Print 2017 Jan.
8
Plasmodium falciparum ookinete expression of plasmepsin VII and plasmepsin X.恶性疟原虫动合子中组织蛋白酶VII和组织蛋白酶X的表达
Malar J. 2016 Feb 24;15:111. doi: 10.1186/s12936-016-1161-5.
9
Enzymatic Characterization of Recombinant Food Vacuole Plasmepsin 4 from the Rodent Malaria Parasite Plasmodium berghei.来自啮齿动物疟原虫伯氏疟原虫的重组食物泡组织蛋白酶4的酶学特性分析
PLoS One. 2015 Oct 28;10(10):e0141758. doi: 10.1371/journal.pone.0141758. eCollection 2015.