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Assembly and activation of heme-deficient neuronal NO synthase with various porphyrins

机译:血红素缺陷型神经元一氧化氮合酶与各种卟啉的组装和激活

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摘要

The heme prosthetic group of NO synthase is critical for catalytic activity as well as assembly of the enzyme to the native homodimeric form. In the current study, we examined if structurally different metal porphyrins could substitute for the native heme prosthetic group in neuronal NO synthase (nNOS) with regard to assembly and catalysis. We established, with the use of a recently developed in vitro method that functionally reconstitutes heme-deficient apo-nNOS, that Fe-mesoporphyrin IX or Fe-deuteroporphyrin IX can substitute for heme and lead to assembly of a functional nNOS, albeit with lower activity. Fe-protoporphyrin IX dimethyl ester or the metal free protoporphyrin IX, however, lead to minimal assembly of nNOS. Protoporphyrin IX compounds where the native Fe was substituted with Zn, Mn, Co, or Sn lead to assembly of nNOS, but no detectable NO was synthesized in the presence of NADPH and L-arginine. Thus, the presence of the metal and propionic acid groups, but not the vinyl moieties, of heme are important structural features in assembly of nNOS. These studies establish that the mechanism of assembly and catalysis of nNOS can be probed with structurally diverse metal porphyrins. (C) 2002 Elsevier Science Inc. All rights reserved. [References: 44]
机译:NO合酶的血红素辅基对于催化活性以及该酶组装成天然同二聚体形式至关重要。在当前的研究中,我们研究了结构上不同的金属卟啉在组装和催化方面是否可以替代神经元NO合酶(nNOS)中的天然血红素假体。我们使用最近开发的功能上重构血红素缺陷型载脂蛋白-nNOS的体外方法,确定了铁-中卟啉IX或铁-氘卟啉IX可以代替血红素并导致功能性nNOS的组装,尽管其活性较低。 。但是,Fe-原卟啉IX二甲基酯或不含金属的原卟啉IX导致nNOS的组装最少。原卟啉IX化合物中的天然Fe被Zn,Mn,Co或Sn取代导致nNOS组装,但在NADPH和L-精氨酸存在下没有合成可检测到的NO。因此,血红素的金属和丙酸基团而不是乙烯基部分的存在是nNOS组装中的重要结构特征。这些研究表明,nNOS的组装和催化机理可以用结构多样的金属卟啉来探测。 (C)2002 Elsevier Science Inc.保留所有权利。 [参考:44]

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