Heterobifunctional Cross-Linking Agents Incorporating Perfluorinated Aryl Azides

被引:29
|
作者
Crocker, Peter J. [2 ]
Imai, Nobuyuki [2 ]
Rajagopalan, Krishnan [2 ]
Boggess, Michael A. [2 ]
Kwiatkowski, Stefan [2 ]
Dwyer, Lori D. [1 ]
Vanaman, Thomas C. [1 ]
Watt, David S. [2 ]
机构
[1] Univ Kentucky, Dept Biochem, Lexington, KY 40506 USA
[2] Univ Kentucky, Dept Chem, Lexington, KY 40506 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
D O I
10.1021/bc00006a008
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
New heterobifunctional cross-linking reagents were developed that possess a photoactive tetrafluorinated phenyl azide as the photoactive terminus and a chemically reactive succinimidyl ester as the electrophilic terminus. These reagents, succinimidyl N-(4-azido-2,3,5,6-tetrafluorobenzoyl)tyrosinate (9) and succinimidyl 2-(4-azido-2,3,5,6-tetrafluorophenyl)thiazole-4-carboxylate (15), were designed to possess either an I-125 or S-35 radiolabel, respectively, In a biochemical study, the latter reagent was coupled to Lys-75 of calmodulin (CaM), and the radioiodinated monoadduct was photochemically cross-linked, in a calcium-dependent manner, to the porcine erythrocyte plasma membrane Ca2+, Mg2+-ATPase. Densitometry scans of the gel indicated a reproducible 22% cross-linking of the CaM with one of the Ca2+, Mg2+-ATPase bands. Since the purification of the Ca2+, Mg2+-ATPase results in micelles having Ca2+, Mg2+-ATPase with its CaM binding site oriented both to the inside and outside of the micelle, the amount of Ca2+, Mg2+-ATPase available for cross-linking was reduced by approximately half, suggesting that the actual cross-linking efficiency was on the order of 40%.
引用
收藏
页码:419 / 424
页数:6
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