Aono S, Honma Y, Ohkubo K, Tawara T, Kamiya T, Nakajima H
School of Materials Science, Japan Advanced Institute of Science and Technology, Nomi-gun, Ishikawa.
J Inorg Biochem. 2000 Nov;82(1-4):51-6. doi: 10.1016/s0162-0134(00)00139-2.
The transcriptional activator CooA from Rhodospirillum rubrum contains a six-coordinate protoheme that acts as a CO sensor in vivo. CO is a physiological effector of CooA and replaces one of the axial ligands of the ferrous heme to form the CO-bound CooA that is active as the transcriptional activator. Cys75 or His77 is coordinated to the ferric and ferrous hemes in CooA, respectively. The redox-controlled ligand exchange between Cys75 and His77 proceeds during the change in the redox state of the heme. The reduction and oxidation midpoint potentials of CooA have been determined to be -320 and -260 mV, respectively. The properties of a functional chimera derived from CRP and CooA suggest that CooA activates the transcription by a similar mechanism to that for CRP at Class II CRP-dependent promoters. Alanine-scanning mutagenesis has revealed that Arg24 and Arg53 of CooA, which will be concerned with the protein-protein interaction with RNA polymerase, are critical amino acid residues for the transcriptional activator activity of CooA, and that Lys26 and Asp94 modulate the activity of CooA.
来自红螺菌的转录激活因子CooA含有一个六配位的原血红素,该原血红素在体内作为一氧化碳(CO)传感器。CO是CooA的生理效应物,它取代亚铁血红素的一个轴向配体,形成作为转录激活因子具有活性的CO结合型CooA。在CooA中,半胱氨酸75(Cys75)和组氨酸77(His77)分别与三价铁和二价铁血红素配位。在血红素氧化还原状态变化过程中,Cys75和His77之间发生氧化还原控制的配体交换。已确定CooA的还原和氧化中点电位分别为-320和-260 mV。源自CRP和CooA的功能性嵌合体的特性表明,在II类CRP依赖性启动子处,CooA通过与CRP类似的机制激活转录。丙氨酸扫描诱变表明,CooA的精氨酸24(Arg24)和精氨酸53(Arg53)与RNA聚合酶的蛋白质-蛋白质相互作用有关,是CooA转录激活活性的关键氨基酸残基,并且赖氨酸26(Lys26)和天冬氨酸94(Asp94)调节CooA的活性。