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甲状腺质膜中Ca2+/NADPH依赖性H2O2生成器:二苯碘鎓的抑制作用

The Ca2+/NADPH-dependent H2O2 generator in thyroid plasma membrane: inhibition by diphenyleneiodonium.

作者信息

Dème D, Doussiere J, De Sandro V, Dupuy C, Pommier J, Virion A

机构信息

INSERM U. 96, Le Kremlin-Bicêtre, France.

出版信息

Biochem J. 1994 Jul 1;301 ( Pt 1)(Pt 1):75-81. doi: 10.1042/bj3010075.

Abstract

The thyroid plasma membrane contains a Ca(2+)-regulated NADPH-dependent H2O2-generating system which provides H2O2 for the peroxidase-catalysed biosynthesis of thyroid hormones. The electron transfer from NADPH to O2 catalysed by this system was studied by using diphenyleneiodonium (DPI), an inhibitor of flavo- and haemo-proteins. The prosthetic group of the H2O2 generator was removed by incubation with 5 mM CHAPS at 40 degrees C, and an active holoenzyme was reconstituted with FAD, but not with FMN. The H2O2-generating system also had an intrinsic Ca(2+)-dependent NADPH:ferricyanide reductase activity which is probably linked to its flavodehydrogenase component (or domain). Both activities, H2O2 production and ferricyanide reductase activity, were inhibited by DPI, with similar K1/2 (2.5 nmol/mg of protein). DPI only inhibited a system reduced with NADPH in the presence of Ca2+. NADPH could not be replaced by NADP+, NADH or sodium dithionite, suggesting the need for specific mild reduction of a redox centre in a particular conformation. Ferricyanide protected both activities against inhibition by DPI; the NADPH:ferricyanide reductase activity was completely protected at a ferricyanide concentration 20 times lower than that needed to protect the H2O2 formation, implying at least two target sites for DPI. One might be the flavodehydrogenase component; the other was beyond, on the entity which transfers the electrons to O2. This second site has not been identified.

摘要

甲状腺质膜含有一个受Ca(2+)调节的依赖NADPH的H2O2生成系统,该系统为过氧化物酶催化的甲状腺激素生物合成提供H2O2。利用黄素蛋白和血红蛋白的抑制剂二苯碘鎓(DPI)研究了该系统催化的从NADPH到O2的电子转移。通过在40℃下与5 mM CHAPS孵育去除H2O2生成器的辅基,并用FAD而不是FMN重建有活性的全酶。H2O2生成系统还具有内在的Ca(2+)依赖性NADPH:铁氰化物还原酶活性,这可能与其黄素脱氢酶组分(或结构域)有关。H2O2生成和铁氰化物还原酶活性这两种活性均被DPI抑制,K1/2相似(2.5 nmol/mg蛋白质)。DPI仅在Ca2+存在下抑制用NADPH还原的系统。NADPH不能被NADP+、NADH或连二亚硫酸钠替代,表明需要对特定构象的氧化还原中心进行特定的温和还原。铁氰化物可保护两种活性免受DPI抑制;NADPH:铁氰化物还原酶活性在铁氰化物浓度比保护H2O2形成所需浓度低20倍时被完全保护,这意味着DPI至少有两个靶位点。一个可能是黄素脱氢酶组分;另一个在将电子转移到O2的实体上更远的位置。第二个位点尚未确定。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ca5/1137145/952c9d173a9a/biochemj00084-0087-a.jpg

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