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氧传感器(Ec DOS)血红素结构域远端的苯丙氨酸113在血红素环境特征中的作用。

Role of Phe113 at the distal side of the heme domain of an oxygen-sensor (Ec DOS) in the characterization of the heme environment.

作者信息

Ito Shinya, Araki Yasuyuki, Tanaka Atsunari, Igarashi Jotaro, Wada Takehiko, Shimizu Toru

机构信息

Institute of Multidisciplinary Research for Advanced Materials, Tohoku University, Sendai, Japan.

出版信息

J Inorg Biochem. 2009 Jul;103(7):989-96. doi: 10.1016/j.jinorgbio.2009.04.009. Epub 2009 May 3.

Abstract

The heme-based oxygen-sensor enzyme from Escherichia coli (Ec DOS) is a heme-regulated phosphodiesterase with activity on cyclic-di-GMP and is composed of an N-terminal heme-bound sensor domain with the PAS structure and a C-terminal functional domain. The activity of Ec DOS is substantially enhanced by the binding of O(2) to the Fe(II)-protoporphyrin IX complex [Fe(II) complex] in the sensor domain. The binding of O(2) to the Fe(II) complex changes the structure of the sensor domain, and this altered structure becomes a signal that is transduced to the functional domain to trigger catalysis. The first step in intra-molecular signal transduction is the binding of O(2) to the Fe(II) complex, and detailed elucidation of this molecular mechanism is thus worthy of exploration. The X-ray crystal structure reveals that Phe113 is located close to the O(2) molecule bound to the Fe(II) complex in the sensor domain. Here, we found that the O(2) association rate constants (>200x10(-3) microM(-1)s(-1): F113L; 26x10(-3) microM(-1)s(-1): F113Y) of the Fe(II) complexes of Phe113 mutants were markedly different from that (51x10(-3) microM(-1)s(-1)) of the wild-type enzyme, and auto-oxidation rates (0.00068 min(-1): F113L; 0.039 min(-1): F113Y) of the Phe113 mutants also differed greatly from that (0.0062 min(-1)) of the wild-type enzyme. We thus suggest that Phe113, residing near the O(2) molecule, has a critical role in optimizing the Fe(II)-O(2) complex for effective regulation of catalysis by the oxygen-sensor enzyme. Interactions of CO and cyanide anion with the mutant proteins were also studied.

摘要

来自大肠杆菌的基于血红素的氧传感器酶(Ec DOS)是一种血红素调节的磷酸二酯酶,对环二鸟苷酸具有活性,由一个带有PAS结构的N端血红素结合传感器结构域和一个C端功能结构域组成。传感器结构域中O₂与亚铁原卟啉IX复合物[Fe(II)复合物]结合会显著增强Ec DOS的活性。O₂与Fe(II)复合物的结合会改变传感器结构域的结构,这种改变的结构成为一种信号,被传导至功能结构域以触发催化作用。分子内信号转导的第一步是O₂与Fe(II)复合物的结合,因此对这一分子机制的详细阐释值得探索。X射线晶体结构显示,Phe113位于传感器结构域中与Fe(II)复合物结合的O₂分子附近。在此,我们发现Phe113突变体的Fe(II)复合物的O₂缔合速率常数(>200×10⁻³ μM⁻¹s⁻¹:F113L;26×10⁻³ μM⁻¹s⁻¹:F113Y)与野生型酶的(51×10⁻³ μM⁻¹s⁻¹)明显不同,并且Phe113突变体的自氧化速率(0.00068 min⁻¹:F113L;0.039 min⁻¹:F113Y)也与野生型酶的(0.0062 min⁻¹)有很大差异。因此我们认为,位于O₂分子附近的Phe113在优化Fe(II)-O₂复合物以有效调节氧传感器酶的催化作用方面起着关键作用。还研究了CO和氰根阴离子与突变蛋白的相互作用。

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