• 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

[Chemosynthetic peptides against foot-and-mouth disease--immune response to free and carrier bound peptides of the VP1 of O1-Kaufbeuren].

作者信息

Liebermann H, Reimann I, Bartels T, Nöckler A, Thalmann G, Furkert J, Dölling R

机构信息

VEB Friedrich-Loeffler-Institut Insel Riems, Betrieb des VEB Kombinat Veterinärimpfstoffe Dessau, DDR Berlin.

出版信息

Arch Exp Veterinarmed. 1990;44(2):189-97.

PMID:1696803
Abstract

Three peptides of main epitope of FMD virus O1-Kaufbeuren, VP1 (16, 21, 31), were found to induce in the 130-160 sequence range, in free and/or carrier-bonded form, virus-neutralising antibodies in guinea pig, rabbit, mouse, swine, and cattle. Five carrier proteins were tested, with thyroglobulin, next to keyhole limpet hemocyanin (KLH), being most effective for 16-peptides (145-160) and 21-peptides (141-160 Tyr161). To protect guinea pig from FMD, minimum dosage of 21-peptide was found to be 2 x 8 micrograms. The immunogenic spectrum of peptides and conjugates proved to be broader than that of monovalent vaccines of inactivated virus. Free peptides were found to be also capable in vitro of inhibiting virus infection.

摘要

相似文献

1
[Chemosynthetic peptides against foot-and-mouth disease--immune response to free and carrier bound peptides of the VP1 of O1-Kaufbeuren].
Arch Exp Veterinarmed. 1990;44(2):189-97.
2
Synthetic peptides against foot-and-mouth disease--immunization with VP1-peptides of type O1-Kaufbeuren.抗口蹄疫合成肽——用O1-考夫博伊伦型VP1肽进行免疫接种
Arch Exp Veterinarmed. 1990;44(6):883-90.
3
Investigation of the influence of peptide-carrier conjugation on the immunological activity of VP1-peptides of foot-and-mouth disease virus O1-Kaufbeuren.肽-载体偶联对口蹄疫病毒O1-考夫博伊伦株VP1肽免疫活性的影响研究
Arch Exp Veterinarmed. 1990;44(6):873-81.
4
[Antigenic structure of the foot-and-mouth disease virus. II. Synthesis of protective peptides from the major immunogenic region of VP1 protein of foot-and-mouth disease virus type A22].[口蹄疫病毒的抗原结构。II. A22型口蹄疫病毒VP1蛋白主要免疫原区保护性肽的合成]
Bioorg Khim. 1988 Oct;14(10):1363-71.
5
Analysis of immune responses in the sheep to synthetic peptides of foot-and-mouth disease virus using ovine polyclonal and monoclonal antibodies.使用绵羊多克隆抗体和单克隆抗体分析绵羊对口蹄疫病毒合成肽的免疫反应。
Immunology. 1990 Jan;69(1):1-7.
6
[Synthetic peptides simulating the protective epitopes of VP1 protein of foot-and-mouth disease virus type O and A].[模拟O型和A型口蹄疫病毒VP1蛋白保护性表位的合成肽]
Bioorg Khim. 1987 Aug;13(8):1132-5.
7
Protection against viral infections with the aid of synthetic peptides. Foot-and-mouth disease as an example.借助合成肽预防病毒感染。以口蹄疫为例。
Biomed Sci. 1990 Jan;1(1):23-32.
8
[Antigenic structure of foot-and-mouth virus. IV. Synthesis and immunogenic properties of new fragments of the VP1 protein of food-and-mouth virus strain A22].
Bioorg Khim. 1989 Sep;15(9):1193-205.
9
[Antigenic structure of the foot-and-mouth disease virus. III. Immunogenic properties of synthetic peptides of the sequence of the immunodominant region of VP1 proteins of the O1K and A22 strains of foot-and-mouth virus].[口蹄疫病毒的抗原结构。III. 口蹄疫病毒O1K和A22株VP1蛋白免疫显性区序列合成肽的免疫原性]
Bioorg Khim. 1989 Sep;15(9):1185-92.
10
[Antigenic structure of the foot-and-mouth-disease virus. I. Synthesis of protective peptides from the major immunogenic region of VP1 protein of foot-and-mouth virus type O1K].[口蹄疫病毒的抗原结构。I. 从O1K型口蹄疫病毒VP1蛋白主要免疫原性区域合成保护性肽段]
Bioorg Khim. 1988 Oct;14(10):1352-62.

引用本文的文献

1
Inhibition of cell adhesion to the virus by synthetic peptides of fiber knob of human adenovirus serotypes 2 and 3 and virus neutralisation by anti-peptide antibodies.人腺病毒2型和3型纤维钮合成肽对细胞与病毒黏附的抑制作用以及抗肽抗体的病毒中和作用。
Virus Res. 1996 Dec;45(2):111-22. doi: 10.1016/s0168-1702(96)01369-x.