• 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

An antagonistic monoclonal antibody (B-N6) specific for the human neurotensin receptor-1.

作者信息

Ovigne J M, Vermot-Desroches C, Lecron J C, Portier M, Lupker J, Pecceu F, Wijdenes J

机构信息

Diaclone, Besançon, France.

出版信息

Neuropeptides. 1998 Jun;32(3):247-56. doi: 10.1016/s0143-4179(98)90044-0.

DOI:10.1016/s0143-4179(98)90044-0
PMID:10189059
Abstract

The neuropeptide neurotensin (NT) interacts with two types of human receptors (hNTR) termed hNTR-1 and hNTR-2. This study describes a monoclonal antibody (MAb) specific for hNTR-1, B-N6. This MAb binds specifically to hNTR-1, but not to hNTR-2 transfected CHO cells. B-N6 and NT display a reciprocal competition and react in a similar way to trypsin, suggesting that the B-N6 epitope is at or close to the NT binding site on the third extracellular loop. Unlike B-N6, NT induces hNTR-1 internalization. Although neither NT-FITC nor B-N6 binding was detected by flow cytometry on different human cells, specific mRNA expression for hNTR-1 was detected in these cells. In CHO cells expressing hNTR-1 and a luciferase gene coupled to the krox24 reporter, B-N6 and the antagonist SR 48692 inhibited NT-induced intracellular activation of krox24 in a dose-dependent manner. From these results it is concluded that B-N6 is an antagonistic anti-hNTR-1 MAb.

摘要

相似文献

1
An antagonistic monoclonal antibody (B-N6) specific for the human neurotensin receptor-1.
Neuropeptides. 1998 Jun;32(3):247-56. doi: 10.1016/s0143-4179(98)90044-0.
2
Activation of mitogen-activated protein kinase couples neurotensin receptor stimulation to induction of the primary response gene Krox-24.丝裂原活化蛋白激酶的激活将神经降压素受体刺激与初级反应基因Krox-24的诱导联系起来。
Biochem J. 1996 Nov 15;320 ( Pt 1)(Pt 1):145-51. doi: 10.1042/bj3200145.
3
In vitro analysis of stable, receptor-selective neurotensin[8-13] analogues.稳定的、受体选择性神经降压素[8-13]类似物的体外分析
J Med Chem. 2003 Sep 11;46(19):4141-8. doi: 10.1021/jm0300633.
4
Topography of the neurotensin (NT)(8-9) binding site of human NT receptor-1 probed with NT(8-13) analogs.
J Pept Res. 2002 Feb;59(2):55-61. doi: 10.1046/j.1397-002x.2001.10946.x.
5
Neurotensin type 1 receptor-mediated activation of krox24, c-fos and Elk-1: preventing effect of the neurotensin antagonists SR 48692 and SR 142948.神经降压素1型受体介导的krox24、c-fos和Elk-1激活:神经降压素拮抗剂SR 48692和SR 142948的预防作用
FEBS Lett. 1998 Jul 31;432(1-2):88-93. doi: 10.1016/s0014-5793(98)00749-2.
6
Biochemical and pharmacological activities of SR 142948A, a new potent neurotensin receptor antagonist.新型强效神经降压素受体拮抗剂SR 142948A的生化及药理活性
J Pharmacol Exp Ther. 1997 Feb;280(2):802-12.
7
Receptor mediated internalization of neurotensin in transfected Chinese hamster ovary cells.转染的中国仓鼠卵巢细胞中神经降压素的受体介导内化作用
Biochem Pharmacol. 1994 Jan 13;47(1):89-91. doi: 10.1016/0006-2952(94)90440-5.
8
Inhibition of neurotensin-induced pancreatic carcinoma growth by a nonpeptide neurotensin receptor antagonist, SR48692.非肽类神经降压素受体拮抗剂SR48692对神经降压素诱导的胰腺癌生长的抑制作用
Cancer. 1997 May 1;79(9):1787-93. doi: 10.1002/(sici)1097-0142(19970501)79:9<1787::aid-cncr22>3.0.co;2-t.
9
Low-affinity neurotensin receptor (NTS2) signaling: internalization-dependent activation of extracellular signal-regulated kinases 1/2.低亲和力神经降压素受体(NTS2)信号传导:细胞外信号调节激酶1/2的内化依赖性激活
Mol Pharmacol. 2004 Dec;66(6):1421-30. doi: 10.1124/mol.104.002303. Epub 2004 Sep 10.
10
Neuropeptide neurotensin stimulates intestinal wound healing following chronic intestinal inflammation.神经肽神经降压素可促进慢性肠道炎症后的肠道伤口愈合。
Am J Physiol Gastrointest Liver Physiol. 2005 Apr;288(4):G621-9. doi: 10.1152/ajpgi.00140.2004.