• 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

100 years lock-and-key concept: are peptide keys shaped and guided to their receptors by the target cell membrane?

作者信息

Schwyzer R

机构信息

Department of Molecular Biology and Biophysics Swiss Federal Institute of Technology.

出版信息

Biopolymers. 1995;37(1):5-16. doi: 10.1002/bip.360370104.

DOI:10.1002/bip.360370104
PMID:7880967
Abstract

The ideas developed in the Membrane Compartments Theory which allow a quantitative prediction of receptor preference are discussed in terms of our present knowledge of opioid and neurokinin receptor structure. Furthermore, conformations of regulatory peptides interacting with artificial lipid membranes are compared with those of chemically constrained molecules that react selectively with different receptor classes. Striking similarities in the topochemistry of molecules with similar activity were observed. The membrane-induced topomers were almost congruent with the artificial topomers that are selectively recognized by the same receptors.

摘要

相似文献

1
100 years lock-and-key concept: are peptide keys shaped and guided to their receptors by the target cell membrane?
Biopolymers. 1995;37(1):5-16. doi: 10.1002/bip.360370104.
2
In search of the 'bio-active conformation'--is it induced by the target cell membrane?寻找“生物活性构象”——它是由靶细胞膜诱导产生的吗?
J Mol Recognit. 1995 Jan-Apr;8(1-2):3-8. doi: 10.1002/jmr.300080103.
3
Structure and regulation of opioid receptors.阿片受体的结构与调控
Biopolymers. 2000;55(4):334-46. doi: 10.1002/1097-0282(2000)55:4<334::AID-BIP1006>3.0.CO;2-S.
4
[A turning point in the knowledge of the structure-function-activity relations of elastin].[弹性蛋白结构-功能-活性关系知识的一个转折点]
J Soc Biol. 2001;195(2):181-93.
5
Recognition of GPCRs by peptide ligands and membrane compartments theory: structural studies of endogenous peptide hormones in membrane environment.肽配体对G蛋白偶联受体的识别与膜区室理论:膜环境中内源性肽激素的结构研究
Biosci Rep. 2006 Apr;26(2):131-58. doi: 10.1007/s10540-006-9014-z.
6
Viral fusion peptides and identification of membrane-interacting segments.
Biochem Biophys Res Commun. 2002 May 17;293(4):1153-60. doi: 10.1016/S0006-291X(02)00353-4.
7
Effect of drastic sequence alteration and D-amino acid incorporation on the membrane binding behavior of lytic peptides.剧烈的序列改变和D-氨基酸掺入对裂解肽膜结合行为的影响。
Biochemistry. 2004 Jun 1;43(21):6393-403. doi: 10.1021/bi049944h.
8
Interactions of amphipathic carrier peptides with membrane components in relation with their ability to deliver therapeutics.两亲性载体肽与膜成分的相互作用及其递送治疗药物的能力。
J Pept Sci. 2006 Dec;12(12):758-65. doi: 10.1002/psc.810.
9
Macromolecular crowding at membrane interfaces: adsorption and alignment of membrane peptides.膜界面处的大分子拥挤现象:膜肽的吸附与排列
J Mol Biol. 2008 Jan 11;375(2):376-85. doi: 10.1016/j.jmb.2007.10.053. Epub 2007 Oct 25.
10
Membrane association, electrostatic sequestration, and cytotoxicity of Gly-Leu-rich peptide orthologs with differing functions.具有不同功能的富含甘氨酸-亮氨酸的肽直系同源物的膜结合、静电隔离及细胞毒性
Biochemistry. 2004 Jul 6;43(26):8391-409. doi: 10.1021/bi0493158.

引用本文的文献

1
Is cholesterol both the lock and key to abnormal transmembrane signals in Autism Spectrum Disorder?胆固醇是否是自闭症谱系障碍中异常跨膜信号的关键?
Lipids Health Dis. 2024 Apr 20;23(1):114. doi: 10.1186/s12944-024-02075-3.
2
Structures of neurokinin 1 receptor in complex with G and G proteins reveal substance P binding mode and unique activation features.神经激肽1受体与G蛋白和G蛋白复合物的结构揭示了P物质的结合模式和独特的激活特征。
Sci Adv. 2021 Dec 10;7(50):eabk2872. doi: 10.1126/sciadv.abk2872. Epub 2021 Dec 8.
3
Membrane-Facilitated Receptor Access and Binding Mechanisms of Long-Acting 2-Adrenergic Receptor Agonists.
长效 2-肾上腺素能受体激动剂的膜介导受体进入和结合机制。
Mol Pharmacol. 2021 Oct;100(4):406-427. doi: 10.1124/molpharm.121.000285. Epub 2021 Aug 1.
4
Does the Lipid Bilayer Orchestrate Access and Binding of Ligands to Transmembrane Orthosteric/Allosteric Sites of G Protein-Coupled Receptors?脂质双层是否调控配体与 G 蛋白偶联受体跨膜正构/变构位点的结合和进入?
Mol Pharmacol. 2019 Nov;96(5):527-541. doi: 10.1124/mol.118.115113. Epub 2019 Apr 8.
5
Link between a high for drug binding and a fast clinical action: to be or not to be?药物结合亲和力高与临床作用迅速之间的关联:存在与否?
Medchemcomm. 2018 Aug 16;9(9):1426-1438. doi: 10.1039/c8md00296g. eCollection 2018 Sep 1.
6
Polypharmacy through Phage Display: Selection of Glucagon and GLP-1 Receptor Co-agonists from a Phage-Displayed Peptide Library.通过噬菌体展示的多药治疗:从噬菌体展示的肽库中选择胰高血糖素和 GLP-1 受体共激动剂。
Sci Rep. 2018 Jan 12;8(1):585. doi: 10.1038/s41598-017-18494-5.
7
Cell membranes… and how long drugs may exert beneficial pharmacological activity in vivo.细胞膜……以及药物在体内可能发挥有益药理活性的时长。
Br J Clin Pharmacol. 2016 Sep;82(3):673-82. doi: 10.1111/bcp.12996. Epub 2016 May 29.
8
Engineering complementary hydrophobic interactions to control β-hairpin peptide self-assembly, network branching, and hydrogel properties.设计互补疏水相互作用以控制β-发夹肽的自组装、网络分支和水凝胶性质。
Biomacromolecules. 2014 Nov 10;15(11):3891-900. doi: 10.1021/bm500874t. Epub 2014 Oct 17.
9
How sterol tilt regulates properties and organization of lipid membranes and membrane insertions.甾醇倾斜如何调节脂质膜和膜插入物的性质和组织。
Chem Phys Lipids. 2013 Apr;169:113-23. doi: 10.1016/j.chemphyslip.2012.12.006. Epub 2013 Jan 3.
10
The spin label amino acid TOAC and its uses in studies of peptides: chemical, physicochemical, spectroscopic, and conformational aspects.自旋标记氨基酸TOAC及其在肽研究中的应用:化学、物理化学、光谱学和构象方面。
Biophys Rev. 2012 Mar;4(1):45-66. doi: 10.1007/s12551-011-0064-5. Epub 2012 Jan 21.