• 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

Electrokinetic charge of the anesthetic-induced bR480 and bR380 spectral forms of bacteriorhodopsin.

作者信息

Taneva S G, Caaveiro J M, Petkanchin I B, Goñi F M

机构信息

Universidad del País Vasco, Departamento de Bioquímica y Biología Molecular, Bilbao, Spain.

出版信息

Biochim Biophys Acta. 1995 Jun 14;1236(2):331-7. doi: 10.1016/0005-2736(95)00074-d.

DOI:10.1016/0005-2736(95)00074-d
PMID:7794973
Abstract

The translational and rotational electrokinetics of the anesthetic-induced spectral transitions bR568-->bR480-->bR380 of bacteriorhodopsin have been investigated. Formation of the bR480 form is associated with an increase of the purple membrane negative electrokinetic charge, while the transformation of bR480 into bR380 is accompanied by a decrease of the membrane negative charge as compared to that of the 480 nm-absorbing form. Removal of anesthetics leads to the back transitions bR480-->bR568 and (in part) bR380-->bR568; however, the electrokinetic charge of the native membranes is not restored. A strong decrease in the electric polarizability and the appearance of a slow polarizability component are also observed in anesthetic-treated membranes. Comparison with the electrokinetic behaviour of partially delipidated membranes and with that of liposomes composed of purple membrane total lipids suggests that: (i) anesthetic molecules partition mainly at the protein/lipid interface inducing irreversible rearrangement of the boundary lipid layer, and (ii) different mode(s) or site(s) of interaction are responsible for the spectral and surface charge effects. The data are compatible with the hypothesis of anesthetics acting through partial dehydration of the membrane surface.

摘要

相似文献

1
Electrokinetic charge of the anesthetic-induced bR480 and bR380 spectral forms of bacteriorhodopsin.
Biochim Biophys Acta. 1995 Jun 14;1236(2):331-7. doi: 10.1016/0005-2736(95)00074-d.
2
Reversible inhibition of proton release activity and the anesthetic-induced acid-base equilibrium between the 480 and 570 nm forms of bacteriorhodopsin.细菌视紫红质在480纳米和570纳米形式之间质子释放活性的可逆抑制以及麻醉诱导的酸碱平衡。
Biophys J. 1996 Feb;70(2):948-61. doi: 10.1016/S0006-3495(96)79638-8.
3
Effects of volatile anesthetics on bacteriorhodopsin in purple membrane, Halobacterium halobium cells and reconstituted vesicles.
Biophys Chem. 1991 Nov;41(2):157-68. doi: 10.1016/0301-4622(91)80015-j.
4
Purple membrane: color, crystallinity, and the effect of dimethyl sulfoxide.紫膜:颜色、结晶度及二甲基亚砜的影响
Biochemistry. 1989 Jul 11;28(14):5971-8. doi: 10.1021/bi00440a038.
5
Effect of lipid-protein interaction on the color of bacteriorhodopsin.脂-蛋白相互作用对细菌视紫红质颜色的影响。
Biochim Biophys Acta. 1989 Feb 28;973(2):257-62. doi: 10.1016/s0005-2728(89)80430-x.
6
Pressure-anesthetic interaction on the molecular conformation of bacteriorhodopsin.压力-麻醉剂对细菌视紫红质分子构象的相互作用。
Ann N Y Acad Sci. 1991;625:767-9. doi: 10.1111/j.1749-6632.1991.tb33914.x.
7
Binding of volatile anesthetics to purple membranes studied by X-ray diffraction.
Toxicol Lett. 1998 Nov 23;100-101:397-403. doi: 10.1016/s0378-4274(98)00213-6.
8
Reversal of the surface charge asymmetry in purple membrane due to single amino acid substitutions.由于单个氨基酸替换导致紫膜表面电荷不对称性的逆转。
Biophys J. 1996 May;70(5):2358-65. doi: 10.1016/S0006-3495(96)79802-8.
9
The quantitative analysis of three action modes of volatile anesthetics on purple membrane.
Biochim Biophys Acta. 2000 Sep 29;1468(1-2):139-49. doi: 10.1016/s0005-2736(00)00253-4.
10
The essential role of specific Halobacterium halobium polar lipids in 2D-array formation of bacteriorhodopsin.嗜盐菌特定极性脂质在细菌视紫红质二维阵列形成中的重要作用。
Biochim Biophys Acta. 1992 Jul 8;1108(1):21-30. doi: 10.1016/0005-2736(92)90110-8.