• 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

产气荚膜梭菌A型肠毒素功能区域的图谱绘制。

Mapping of functional regions of Clostridium perfringens type A enterotoxin.

作者信息

Hanna P C, Wieckowski E U, Mietzner T A, McClane B A

机构信息

Department of Molecular Genetics and Biochemistry, University of Pittsburgh School of Medicine, Pennsylvania 15261-2072.

出版信息

Infect Immun. 1992 May;60(5):2110-4. doi: 10.1128/iai.60.5.2110-2114.1992.

DOI:10.1128/iai.60.5.2110-2114.1992
PMID:1373406
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC257123/
Abstract

Studies were conducted to allow construction of an initial map of the structure-versus-function relationship of the Clostridium perfringens type A enterotoxin (CPE). Removal of the N-terminal 25 amino acids of CPE increased the primary cytotoxic effect of CPE but did not affect binding. CPE sequences required for at least four epitopes were also identified.

摘要

开展了多项研究,以构建A型产气荚膜梭菌肠毒素(CPE)结构与功能关系的初步图谱。去除CPE的N端25个氨基酸会增强CPE的主要细胞毒性作用,但不影响其结合。还确定了至少四个表位所需的CPE序列。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6076/257123/13aa91cb847b/iai00029-0398-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6076/257123/0a165314386b/iai00029-0398-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6076/257123/13aa91cb847b/iai00029-0398-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6076/257123/0a165314386b/iai00029-0398-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6076/257123/13aa91cb847b/iai00029-0398-b.jpg

相似文献

1
Mapping of functional regions of Clostridium perfringens type A enterotoxin.产气荚膜梭菌A型肠毒素功能区域的图谱绘制。
Infect Immun. 1992 May;60(5):2110-4. doi: 10.1128/iai.60.5.2110-2114.1992.
2
Analysis of multiple antigenic determinants of Clostridium perfringens enterotoxin as revealed by use of different synthetic peptides.利用不同合成肽揭示产气荚膜梭菌肠毒素的多种抗原决定簇分析
J Vet Med Sci. 1994 Dec;56(6):1047-50. doi: 10.1292/jvms.56.1047.
3
Deletion analysis of the Clostridium perfringens enterotoxin.产气荚膜梭菌肠毒素的缺失分析
Infect Immun. 1997 Mar;65(3):1014-22. doi: 10.1128/IAI.65.3.1014-1022.1997.
4
Identification of a Clostridium perfringens enterotoxin region required for large complex formation and cytotoxicity by random mutagenesis.通过随机诱变鉴定产气荚膜梭菌肠毒素形成大复合物和细胞毒性所需的区域。
Infect Immun. 1999 Nov;67(11):5634-41. doi: 10.1128/IAI.67.11.5634-5641.1999.
5
Innovative and Highly Sensitive Detection of Enterotoxin Based on Receptor Interaction and Monoclonal Antibodies.基于受体相互作用和单克隆抗体的肠毒素创新高灵敏度检测
Toxins (Basel). 2021 Apr 8;13(4):266. doi: 10.3390/toxins13040266.
6
An overview of Clostridium perfringens enterotoxin.
Toxicon. 1996 Nov-Dec;34(11-12):1335-43. doi: 10.1016/s0041-0101(96)00101-8.
7
A conjugated synthetic peptide corresponding to the C-terminal region of Clostridium perfringens type A enterotoxin elicits an enterotoxin-neutralizing antibody response in mice.一种与A型产气荚膜梭菌肠毒素C端区域相对应的偶联合成肽可在小鼠体内引发肠毒素中和抗体反应。
Infect Immun. 1992 Sep;60(9):3947-51. doi: 10.1128/iai.60.9.3947-3951.1992.
8
The complex interactions between Clostridium perfringens enterotoxin and epithelial tight junctions.产气荚膜梭菌肠毒素与上皮紧密连接之间的复杂相互作用。
Toxicon. 2001 Nov;39(11):1781-91. doi: 10.1016/s0041-0101(01)00164-7.
9
A recombinant C-terminal toxin fragment provides evidence that membrane insertion is important for Clostridium perfringens enterotoxin cytotoxicity.一种重组C端毒素片段表明,膜插入对于产气荚膜梭菌肠毒素的细胞毒性很重要。
Mol Microbiol. 1991 Jan;5(1):225-30. doi: 10.1111/j.1365-2958.1991.tb01843.x.
10
Trypsin activation of enterotoxin from Clostridium perfringens type A: fragmentation and some physicochemical properties.
Biochim Biophys Acta. 1981 May 29;668(3):325-32. doi: 10.1016/0005-2795(81)90165-3.

引用本文的文献

1
Processing of Enterotoxin by Intestinal Proteases.肠道蛋白酶对肠毒素的加工处理
Toxins (Basel). 2025 Apr 1;17(4):170. doi: 10.3390/toxins17040170.
2
Processing Enterotoxin by Intestinal Proteases.肠道蛋白酶对肠毒素的处理
bioRxiv. 2025 Feb 11:2025.02.11.637699. doi: 10.1101/2025.02.11.637699.
3
Disruption of Claudin-Made Tight Junction Barriers by Enterotoxin: Insights from Structural Biology.肠毒素破坏紧密连接屏障:结构生物学的见解。

本文引用的文献

1
Protein measurement with the Folin phenol reagent.使用福林酚试剂进行蛋白质测定。
J Biol Chem. 1951 Nov;193(1):265-75.
2
Monoclonal antibodies (O1 to O4) to oligodendrocyte cell surfaces: an immunocytological study in the central nervous system.针对少突胶质细胞表面的单克隆抗体(O1至O4):中枢神经系统的免疫细胞化学研究
Dev Biol. 1981 Apr 30;83(2):311-27. doi: 10.1016/0012-1606(81)90477-2.
3
Osmotic stabilizers differentially inhibit permeability alterations induced in Vero cells by Clostridium perfringens enterotoxin.渗透稳定剂对产气荚膜梭菌肠毒素诱导的Vero细胞通透性改变具有不同程度的抑制作用。
Cells. 2022 Mar 5;11(5):903. doi: 10.3390/cells11050903.
4
Tight Junction Modulating Bioprobes for Drug Delivery System to the Brain: A Review.用于脑药物递送系统的紧密连接调节生物探针:综述
Pharmaceutics. 2020 Dec 19;12(12):1236. doi: 10.3390/pharmaceutics12121236.
5
Sialidases From and Their Inhibitors.唾液酸酶及其抑制剂。
Front Cell Infect Microbiol. 2020 Jan 10;9:462. doi: 10.3389/fcimb.2019.00462. eCollection 2019.
6
Development of Adjuvant-Free Bivalent Food Poisoning Vaccine by Augmenting the Antigenicity of Enterotoxin.无佐剂双价食源性致病菌疫苗的研制:增强肠毒素抗原性。
Front Immunol. 2018 Oct 9;9:2320. doi: 10.3389/fimmu.2018.02320. eCollection 2018.
7
Enterotoxic Clostridia: Enteric Diseases.肠毒素梭菌:肠道疾病。
Microbiol Spectr. 2018 Sep;6(5). doi: 10.1128/microbiolspec.GPP3-0003-2017.
8
Clostridium perfringens Sialidases: Potential Contributors to Intestinal Pathogenesis and Therapeutic Targets.产气荚膜梭菌唾液酸酶:肠道发病机制的潜在促成因素及治疗靶点
Toxins (Basel). 2016 Nov 19;8(11):341. doi: 10.3390/toxins8110341.
9
The interaction of Clostridium perfringens enterotoxin with receptor claudins.产气荚膜梭菌肠毒素与紧密连接蛋白受体的相互作用。
Anaerobe. 2016 Oct;41:18-26. doi: 10.1016/j.anaerobe.2016.04.011. Epub 2016 Apr 16.
10
Clostridium perfringens Enterotoxin: Action, Genetics, and Translational Applications.产气荚膜梭菌肠毒素:作用、遗传学及转化应用
Toxins (Basel). 2016 Mar 16;8(3):73. doi: 10.3390/toxins8030073.
Biochim Biophys Acta. 1984 Oct 17;777(1):99-106. doi: 10.1016/0005-2736(84)90501-7.
4
Sequence of the amino-terminal part of enterotoxin from Clostridium perfringens type A: identification of points of trypsin activation.A型产气荚膜梭菌肠毒素氨基末端部分的序列:胰蛋白酶激活位点的鉴定。
Infect Immun. 1983 Jun;40(3):943-9. doi: 10.1128/iai.40.3.943-949.1983.
5
Inhibition of protein synthesis by a tryptic polypeptide of Clostridium perfringens type A enterotoxin.A型产气荚膜梭菌肠毒素的胰蛋白酶多肽对蛋白质合成的抑制作用。
Biochim Biophys Acta. 1982 Oct 20;708(1):6-11. doi: 10.1016/0167-4838(82)90196-0.
6
Binding of Clostridium perfringens [125I]enterotoxin to rabbit intestinal cells.产气荚膜梭菌[125I]肠毒素与兔肠道细胞的结合。
Biochemistry. 1980 Oct 14;19(21):4801-7. doi: 10.1021/bi00562a014.
7
Trypsin activation of enterotoxin from Clostridium perfringens type A: fragmentation and some physicochemical properties.
Biochim Biophys Acta. 1981 May 29;668(3):325-32. doi: 10.1016/0005-2795(81)90165-3.
8
Characterization of membrane permeability alterations induced in Vero cells by Clostridium perfringens enterotoxin.产气荚膜梭菌肠毒素诱导Vero细胞中膜通透性改变的特征分析
Biochim Biophys Acta. 1980 Aug 14;600(3):974-85. doi: 10.1016/0005-2736(80)90499-x.
9
Cleavage of structural proteins during the assembly of the head of bacteriophage T4.在噬菌体T4头部组装过程中结构蛋白的切割
Nature. 1970 Aug 15;227(5259):680-5. doi: 10.1038/227680a0.
10
Primary action of Clostridium perfringens type A enterotoxin on HeLa and Vero cells in the absence of extracellular calcium: rapid and characteristic changes in membrane permeability.A型产气荚膜梭菌肠毒素在无细胞外钙的情况下对HeLa细胞和Vero细胞的主要作用:膜通透性的快速且特征性变化
Biochem Biophys Res Commun. 1986 Dec 15;141(2):704-10. doi: 10.1016/s0006-291x(86)80229-7.