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首页> 外文期刊>Antioxidants and redox signalling >How do heme-protein sensors exclude oxygen? Lessons learned from cytochrome c??, nostoc puntiforme heme nitric oxide/oxygen-binding domain, and soluble guanylyl cyclase
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How do heme-protein sensors exclude oxygen? Lessons learned from cytochrome c??, nostoc puntiforme heme nitric oxide/oxygen-binding domain, and soluble guanylyl cyclase

机译:血红蛋白传感器如何排除氧气? 来自细胞色素C的经验教训,NOSTOC Puntifice血红素一氧化氮/氧合域,和可溶性观冠酶

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摘要

Significance: Ligand selectivity for dioxygen (O2), carbon monoxide (CO), and nitric oxide (NO) is critical for signal transduction and is tailored specifically for each heme-protein sensor. Key NO sensors, such as soluble guanylyl cyclase (sGC), specifically recognized low levels of NO and achieve a total O2 exclusion. Several mechanisms have been proposed to explain the O2 insensitivity, including lack of a hydrogen bond donor and negative electrostatic fields to selectively destabilize bound O 2, distal steric hindrance of all bound ligands to the heme iron, and restriction of in-plane movements of the iron atom. Recent Advances: Crystallographic structures of the gas sensors, Thermoanaerobacter tengcongensis heme-nitric oxide/oxygen-binding domain (Tt H-NOX1) or Nostoc puntiforme (Ns) H-NOX, and measurements of O2 binding to site-specific mutants of Tt H-NOX and the truncated ?? subunit of sGC suggest the need for a H-bonding donor to facilitate O2 binding. Critical Issues: However, the O2 insensitivity of full length sGC with a site-specific replacement of isoleucine by a tyrosine on residue 145 and the very slow autooxidation of Ns H-NOX and cytochrome c?? suggest that more complex mechanisms have evolved to exclude O2 but retain high affinity NO binding. A combined graphical analysis of ligand binding data for libraries of heme sensors, globins, and model heme shows that the NO sensors dramatically inhibit the formation of six-coordinated NO, CO, and O2 complexes by direct distal steric hindrance (cyt c??), proximal constraints of in-plane iron movement (sGC), or combinations of both following a sliding scale rule. High affinity NO binding in H-NOX proteins is achieved by multiple NO binding steps that produce a high affinity five-coordinate NO complex, a mechanism that also prevents NO dioxygenation. Future Directions: Knowledge advanced by further extensive test of this sliding scale rule hypothesis should be valuable in guiding novel designs for heme based sensors. ? 2012 Mary Ann Liebert, Inc.
机译:重要性:二恶英(O2),一氧化碳(CO)和一氧化氮(NO)的配体选择性对于信号转导,专门针对每个血红蛋白传感器定制。键无传感器,例如可溶性瓜达林环酶(SGC),具体识别出低水平的NO并达到总O2排除。已经提出了几种机制来解释O2不敏感性,包括缺乏氢键供体和负静电场,以选择性地使所有结合的配体与血红素铁相结合的结合O 2,远端空间阻力,并限制面内运动铁原子。最近的进展:气体传感器的晶体结构,Tentcancactersis血红素一氧化氮/氧结合结构域(TT H-NOX1)或NOSTOC Puntifice(NS)H-NOx,以及测量与TT H的位点特异性突变体的测量结果-Nox和截短的?? SGC的亚基表明需要H键合供体以促进O2结合。关键问题:然而,全长SGC的O2不敏感性通过酪氨酸对残留物145的酪氨酸特异性替代物,对NS H-NOx的非常缓慢的自身氧化和细胞色素C ??建议更复杂的机制已经进化为排除O2,但保留高亲和力没有任何约束力。血红素传感器,球状粒细胞文库的配体结合数据的组合图分析表明,NO传感器通过直接远端空间阻断(Cyt C ??)显着抑制形成六种协调的NO,CO和O2复合物,面内铁运动(SGC)的近端约束,或在滑动尺度规则之后的组合。高亲和力在H-NOx蛋白中没有结合通过多重无结合步骤来实现,其产生高亲和力的五坐标无复合物,该机制也防止了没有二氧化的机理。未来的方向:通过进一步广泛考验的知识推动该滑动规则规则假设应为引导基于血红素传感器的新设计是有价值的。还2012年玛丽安莱伯特,Inc。

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  • 来源
    《Antioxidants and redox signalling 》 |2012年第9期| 共18页
  • 作者单位

    Division of Hematology University of Texas Health Science Center at Houston 6431 Fannin St.;

    Division of Cardiology Department of Internal Medicine University of Texas Health Science Center;

    Division of Hematology University of Texas Health Science Center at Houston 6431 Fannin St.;

    Department of Biochemistry and Cell Biology W.M. Keck Center for Computational Biology Rice;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 基础医学 ;
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