• 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

恶性疟原虫的葡萄糖-6-磷酸脱氢酶活性

Glucose-6-phosphate dehydrogenase activity of the malaria parasite Plasmodium falciparum.

作者信息

Ling I T, Wilson R J

机构信息

National Institute for Medical Research, London, U.K.

出版信息

Mol Biochem Parasitol. 1988 Oct;31(1):47-56. doi: 10.1016/0166-6851(88)90144-2.

DOI:10.1016/0166-6851(88)90144-2
PMID:3054541
Abstract

Schizonts of Plasmodium falciparum, grown either in normal or glucose-6-phosphate dehydrogenase (G6PDH) deficient human red cells, contain an electrophoretically slow-moving form of G6PDH. The slow mobility of the G6PDH in non-dissociating polyacrylamide gels is due to its large size (Mr ca. 450,000) rather than to its charge. The activity of this enzyme was less than 10% of normal red cell G6PDH. These characteristics of the parasite-associated G6PDH were unaltered when parasites were grown in red cells from a G6PDH A+B+ heterozygote or following the introduction of a heterologous G6PDH into resealed ghosts. Differential absorption of the parasite-associated and red cell G6PDHs was demonstrated with antisera containing antibodies to red cell G6PDH. These studies show that a novel form of G6PDH is associated with P. falciparum in normal red cells without the requirements for induction by one or several cycles of multiplication in G6PDH deficient red cells.

摘要

恶性疟原虫的裂殖体,无论是在正常的还是葡萄糖-6-磷酸脱氢酶(G6PDH)缺乏的人红细胞中生长,都含有一种电泳迁移缓慢的G6PDH形式。在非解离聚丙烯酰胺凝胶中,G6PDH迁移缓慢是由于其分子量大(约450,000道尔顿),而非电荷原因。这种酶的活性不到正常红细胞G6PDH的10%。当寄生虫在G6PDH A+B+杂合子的红细胞中生长或在重新封闭的血影中引入异源G6PDH后,寄生虫相关G6PDH的这些特性并未改变。用含有抗红细胞G6PDH抗体的抗血清证明了寄生虫相关G6PDH和红细胞G6PDH的差异吸收。这些研究表明,一种新型的G6PDH与正常红细胞中的恶性疟原虫相关,无需在G6PDH缺乏的红细胞中经过一个或几个增殖周期诱导。

相似文献

1
Glucose-6-phosphate dehydrogenase activity of the malaria parasite Plasmodium falciparum.恶性疟原虫的葡萄糖-6-磷酸脱氢酶活性
Mol Biochem Parasitol. 1988 Oct;31(1):47-56. doi: 10.1016/0166-6851(88)90144-2.
2
Detection of glucose-6-phosphate dehydrogenase in malarial parasites.疟原虫中葡萄糖-6-磷酸脱氢酶的检测
Mol Biochem Parasitol. 1981 Feb;2(3-4):197-204. doi: 10.1016/0166-6851(81)90100-6.
3
Expression and characterization of glucose-6-phosphate dehydrogenase of Plasmodium falciparum.恶性疟原虫葡萄糖-6-磷酸脱氢酶的表达与特性分析
Mol Biochem Parasitol. 1990 Jun;41(1):83-91. doi: 10.1016/0166-6851(90)90099-8.
4
Pathways for the reduction of oxidized glutathione in the Plasmodium falciparum-infected erythrocyte: can parasite enzymes replace host red cell glucose-6-phosphate dehydrogenase?恶性疟原虫感染红细胞中氧化型谷胱甘肽的还原途径:疟原虫酶能否替代宿主红细胞葡萄糖-6-磷酸脱氢酶?
Blood. 1986 Mar;67(3):827-30.
5
Glucose-6-phosphate dehydrogenase of malaria parasite Plasmodium falciparum.恶性疟原虫的葡萄糖-6-磷酸脱氢酶
Blood. 1987 May;69(5):1528-30.
6
Adaptation of Plasmodium falciparum to glucose 6-phosphate dehydrogenase-deficient host red cells by production of parasite-encoded enzyme.恶性疟原虫通过产生寄生虫编码的酶来适应葡萄糖-6-磷酸脱氢酶缺乏的宿主红细胞。
Nature. 1985;313(6005):793-5. doi: 10.1038/313793a0.
7
Malarial parasite hexokinase and hexokinase-dependent glutathione reduction in the Plasmodium falciparum-infected human erythrocyte.疟原虫己糖激酶与恶性疟原虫感染的人体红细胞中己糖激酶依赖性谷胱甘肽还原作用
J Biol Chem. 1987 Nov 15;262(32):15678-82.
8
Early phagocytosis of glucose-6-phosphate dehydrogenase (G6PD)-deficient erythrocytes parasitized by Plasmodium falciparum may explain malaria protection in G6PD deficiency.被恶性疟原虫寄生的葡萄糖-6-磷酸脱氢酶(G6PD)缺乏的红细胞早期被吞噬,这可能解释了G6PD缺乏症对疟疾的保护作用。
Blood. 1998 Oct 1;92(7):2527-34.
9
The enzymes of the glycolytic pathway in erythrocytes infected with Plasmodium falciparum malaria parasites.感染恶性疟原虫的红细胞中糖酵解途径的酶。
Blood. 1988 Dec;72(6):1922-5.
10
An Optimized Dihydrodibenzothiazepine Lead Compound (SBI-0797750) as a Potent and Selective Inhibitor of Plasmodium falciparum and P. vivax Glucose 6-Phosphate Dehydrogenase 6-Phosphogluconolactonase.一种优化的二氢二苯并噻嗪先导化合物(SBI-0797750),作为一种有效的、选择性的恶性疟原虫和间日疟原虫葡萄糖-6-磷酸脱氢酶-6-磷酸葡糖酸内酯酶抑制剂。
Antimicrob Agents Chemother. 2022 Apr 19;66(4):e0210921. doi: 10.1128/aac.02109-21. Epub 2022 Mar 10.

引用本文的文献

1
Fused Enzyme Glucose-6-Phosphate Dehydrogenase::6-Phosphogluconolactonase (G6PD::6PGL) as a Potential Drug Target in , , and .融合酶葡萄糖-6-磷酸脱氢酶::6-磷酸葡萄糖酸内酯酶(G6PD::6PGL)作为[具体疾病名称1]、[具体疾病名称2]和[具体疾病名称3]中的潜在药物靶点 。 需注意,原文中“in , , and.”处应补充具体疾病信息,以上译文为根据已有内容的完整翻译。
Microorganisms. 2024 Jan 5;12(1):112. doi: 10.3390/microorganisms12010112.
2
High-throughput screening for small-molecule inhibitors of plasmodium falciparum glucose-6-phosphate dehydrogenase 6-phosphogluconolactonase.恶性疟原虫葡萄糖-6-磷酸脱氢酶6-磷酸葡萄糖酸内酯酶小分子抑制剂的高通量筛选
J Biomol Screen. 2012 Jul;17(6):738-51. doi: 10.1177/1087057112442382. Epub 2012 Apr 11.