• 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

重组人肾素色氨酸残基对猝灭剂的不可及性。

Inaccessibility of tryptophan residues of recombinant human renin to quenching agents.

作者信息

Epps D E, Poorman R, Hui J, Carlson W, Heinrikson R

出版信息

J Biol Chem. 1987 Aug 5;262(22):10570-3.

PMID:3301839
Abstract

The fluorescence quenching of the three tryptophan residues of recombinant human renin was determined using ionic and penetrating quenchers. Tryptophans 44,200, and 312 of recombinant human renin were found to be totally inaccessible to the ionic quenchers cesium and iodide and only partially accessible to the penetrating quencher acrylamide. The renin had a fluorescence emission maximum at 325 nm which was made up of three separate components as determined by second derivative spectroscopy. These data are in accord with solvent accessibility calculations from three-dimensional models of human renin but differ from findings published previously from similar analysis of mouse submandibular gland renin (Quay, S. C., Heropoulous, A., Commes, K., Dzau, V. J. (1985) J. Biol. Chem. 260, 15055-15058), which is 68% identical in sequence to human renin.

摘要

利用离子型淬灭剂和可穿透性淬灭剂测定了重组人肾素三个色氨酸残基的荧光淬灭情况。发现重组人肾素的色氨酸44、200和312完全无法被离子型淬灭剂铯和碘化物接触,而仅部分可被可穿透性淬灭剂丙烯酰胺接触。肾素在325nm处有最大荧光发射峰,通过二阶导数光谱法测定,该峰由三个独立成分组成。这些数据与根据人肾素三维模型进行的溶剂可及性计算结果一致,但与先前发表的对小鼠下颌下腺肾素进行类似分析的结果不同(奎伊,S.C.,赫罗普洛斯,A.,科姆斯,K.,Dzau,V.J.(1985年)《生物化学杂志》260,15055 - 15058),小鼠下颌下腺肾素与人类肾素的序列同源性为68%。

相似文献

1
Inaccessibility of tryptophan residues of recombinant human renin to quenching agents.重组人肾素色氨酸残基对猝灭剂的不可及性。
J Biol Chem. 1987 Aug 5;262(22):10570-3.
2
Characterization of the tryptophan environments of interleukins 1 alpha and 1 beta by fluorescence quenching and lifetime measurements.通过荧光猝灭和寿命测量对白细胞介素1α和1β的色氨酸环境进行表征。
Arch Biochem Biophys. 1989 Nov 15;275(1):82-91. doi: 10.1016/0003-9861(89)90352-4.
3
Quenching of tryptophan fluorescence in bovine lens proteins by acrylamide and iodide.丙烯酰胺和碘化物对牛晶状体蛋白中色氨酸荧光的猝灭作用。
Curr Eye Res. 1988 Mar;7(3):237-45. doi: 10.3109/02713688809047028.
4
Fluorescence quenching studies of bovine growth hormone in several conformational states.处于几种构象状态的牛生长激素的荧光猝灭研究。
Biochim Biophys Acta. 1988 Jul 20;955(2):154-63. doi: 10.1016/0167-4838(88)90189-6.
5
Fluorescence quenching and time-resolved fluorescence studies of alpha-mannosidase from Aspergillus fischeri (NCIM 508).费氏曲霉(NCIM 508)α-甘露糖苷酶的荧光猝灭和时间分辨荧光研究
J Fluoresc. 2007 Nov;17(6):599-605. doi: 10.1007/s10895-007-0227-8. Epub 2007 Sep 6.
6
A photoreversible conformational change in 124 kDa Avena phytochrome.124千道尔顿燕麦光敏色素中的一种光可逆构象变化。
Biochim Biophys Acta. 1988 Dec 7;936(3):395-405. doi: 10.1016/0005-2728(88)90016-3.
7
Acrylamide and iodide fluorescence quenching as a structural probe of tryptophan microenvironment in bovine lens crystallins.丙烯酰胺和碘化物荧光猝灭作为牛晶状体晶状体蛋白中色氨酸微环境的结构探针。
Curr Eye Res. 1986 Aug;5(8):611-9. doi: 10.3109/02713688609015126.
8
Tryptophanyl fluorescence quenching of urocanase from Pseudomonas putida by acrylamide, cesium, iodide, and imidazolepropionate.
Photochem Photobiol. 1985 Aug;42(2):107-12. doi: 10.1111/j.1751-1097.1985.tb01546.x.
9
Fluorescence of native single-Trp mutants in the lactose permease from Escherichia coli: structural properties and evidence for a substrate-induced conformational change.大肠杆菌乳糖通透酶中天然单色氨酸突变体的荧光:结构特性及底物诱导构象变化的证据
Protein Sci. 1995 Nov;4(11):2310-8. doi: 10.1002/pro.5560041108.
10
Steady state and picosecond time-resolved fluorescence studies on native, desulpho and deflavo xanthine oxidase.天然型、脱硫型和脱黄素型黄嘌呤氧化酶的稳态及皮秒时间分辨荧光研究
Biochim Biophys Acta. 2000 Sep 29;1481(2):273-82. doi: 10.1016/s0167-4838(00)00136-9.

引用本文的文献

1
The constituent tryptophans and bisANS as fluorescent probes of the active site and of a secondary binding site of stromelysin-1 (MMP-3).
J Protein Chem. 1998 Oct;17(7):699-712. doi: 10.1007/BF02780973.