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诱导型一氧化氮合酶中 FMN-血红素电子转移过程中同工型特异性丝氨酸残基的作用。

Role of an isoform-specific serine residue in FMN-heme electron transfer in inducible nitric oxide synthase.

机构信息

Department of Pharmaceutical Sciences, College of Pharmacy, University of New Mexico, Albuquerque, NM 87131, USA.

出版信息

J Biol Inorg Chem. 2012 Jun;17(5):675-85. doi: 10.1007/s00775-012-0887-y. Epub 2012 Mar 10.

Abstract

In the crystal structure of a calmodulin (CaM)-bound FMN domain of human inducible nitric oxide synthase (NOS), the CaM-binding region together with CaM forms a hinge, and pivots on an R536(NOS)/E47(CaM) pair (Xia et al. J Biol Chem 284:30708-30717, 2009). Notably, isoform-specific human inducible NOS S562 and C563 residues form hydrogen bonds with the R536 residue through their backbone oxygens. In this study, we investigated the roles of the S562 and C563 residues in the NOS FMN-heme interdomain electron transfer (IET), the rates of which can be used to probe the interdomain FMN/heme alignment. Human inducible NOS S562K and C563R mutants of an oxygenase/FMN (oxyFMN) construct were made by introducing charged residues at these sites as found in human neuronal NOS and endothelial NOS isoforms, respectively. The IET rate constant of the S562K mutant is notably decreased by one third, and its flavin fluorescence intensity per micromole per liter is diminished by approximately 24 %. These results suggest that a positive charge at position 562 destabilizes the hydrogen-bond-mediated NOS/CaM alignment, resulting in slower FMN-heme IET in the mutant. On the other hand, the IET rate constant of the C563R mutant is similar to that of the wild-type, indicating that the mutational effect is site-specific. Moreover, the human inducible NOS oxyFMN R536E mutant was constructed to disrupt the bridging CaM/NOS interaction, and its FMN-heme IET rate was decreased by 96 %. These results demonstrated a new role of the isoform-specific serine residue of the key CaM/FMN(NOS) bridging site in regulating the FMN-heme IET (possibly by tuning the alignment of the FMN and heme domains).

摘要

在人诱导型一氧化氮合酶(NOS)的黄素单核苷酸(FMN)结构域与钙调蛋白(CaM)结合的晶体结构中,CaM 结合区与 CaM 一起形成一个铰链,并以 R536(NOS)/E47(CaM)对为枢轴(Xia 等人,J Biol Chem 284:30708-30717, 2009)。值得注意的是,同种型特异性人诱导型 NOS 的 S562 和 C563 残基通过其骨架氧与 R536 残基形成氢键。在这项研究中,我们研究了 S562 和 C563 残基在 NOS FMN-血红素间域电子转移(IET)中的作用,其速率可用于探测间域 FMN/血红素的排列。通过在这些位点引入人神经元 NOS 和内皮 NOS 同工型中发现的带电残基,构建了人诱导型 NOS S562K 和 C563R 突变体的加氧酶/FMN(oxyFMN)构建体。S562K 突变体的 IET 速率常数显著降低了三分之一,其每微摩尔每升的黄素荧光强度减少了约 24%。这些结果表明,位置 562 上的正电荷使 NOS/CaM 排列的氢键介导不稳定,导致突变体中 FMN-血红素 IET 变慢。另一方面,C563R 突变体的 IET 速率常数与野生型相似,表明突变的影响是特异性的。此外,构建了人诱导型 NOS oxyFMN R536E 突变体以破坏桥接 CaM/NOS 相互作用,其 FMN-血红素 IET 速率降低了 96%。这些结果表明关键 CaM/FMN(NOS)桥接位点的同种型特异性丝氨酸残基在调节 FMN-血红素 IET 中具有新的作用(可能通过调整 FMN 和血红素结构域的排列)。

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