Yoon Taejin, Cowan J A
Evans Laboratory of Chemistry, The Ohio State University, 100 West 18th Avenue, Columbus 43210, USA.
J Am Chem Soc. 2003 May 21;125(20):6078-84. doi: 10.1021/ja027967i.
ISU (eukaryotes) and IscU (prokaryotes) are a homologous family of proteins that appear to provide a platform for assembly of [2Fe-2S] centers prior to delivery to an apo target protein. The intermediate [2Fe-2S] ISU-bound cluster is formed by delivery of iron and sulfur to the apo ISU, with the latter delivered through an IscS-mediated reaction. The identity of the iron donor has thus far not been established. In this paper we demonstrate human frataxin to bind from six to seven iron ions. Iron binding to frataxin has been quantitated by iron-dependent fluorescence measurements [K(D)(Fe(3+)) approximately 11.7 microM; (K(D)(Fe(2+)) approximately 55.0 microM] and isothermal titration calorimetry (ITC) [K(D)(Fe(3+)) approximately 10.2 microM]. Enthalpies and entropies for ferric ion binding were determined from calorimetric measurements. Both fluorescence (K(D) 0.45 microM) and ITC measurements (K(D) 0.15 microM) demonstrate holo frataxin to form a complex with ISU with sub-micromolar binding affinities. Significantly, apo frataxin does not bind to ISU, suggesting an important role for iron in cross-linking the two proteins and/or stabilizing the structure of frataxin that is recognized by ISU. Holo frataxin is also shown to mediate the transfer of iron from holo frataxin to nucleation sites for [2Fe-2S] cluster formation on ISU. We have demonstrated elsewhere [J. Am. Chem. Soc. 2002, 124, 8774-8775] that this iron-bound form of ISU is viable for assembly of holo ISU, either by subsequent addition of sulfide or by NifS-mediated sulfur delivery. Provision of holo frataxin and inorganic sulfide is sufficient for cluster assembly in up to 70% yield. With NifS as a sulfur donor, yields in excess of 70% of holo ISU were obtained. Both UV-vis and CD spectroscopic characteristics were found to be consistent with those of previously characterized ISU proteins. The time course for cluster assembly was monitored from the 456 nm absorbance of holo ISU formed during the [2Fe-2S] cluster assembly reaction. A kinetic rate constant k(obs) approximately 0.075 min(-)(1) was determined with 100 microM ISU, 2.4 mM Na(2)S, and 40 microM holo frataxin in 50 mM Tris-HCl (pH 7.5) with 4.3 mM DTT. Similar rates were obtained for NifS-mediated sulfur delivery, consistent with iron release from frataxin as a rate-limiting step in the cluster assembly reaction.
ISU(真核生物)和IscU(原核生物)是一类同源蛋白家族,它们似乎为[2Fe-2S]中心在传递给无辅基靶蛋白之前的组装提供了一个平台。中间的[2Fe-2S]与ISU结合的簇是通过将铁和硫传递到无辅基的ISU上形成的,后者通过IscS介导的反应传递。到目前为止,铁供体的身份尚未确定。在本文中,我们证明人frataxin能结合6到7个铁离子。通过铁依赖性荧光测量[K(D)(Fe(3+))约为11.7 microM;(K(D)(Fe(2+))约为55.0 microM]和等温滴定量热法(ITC)[K(D)(Fe(3+))约为10.2 microM]对铁与frataxin的结合进行了定量。通过量热测量确定了铁离子结合的焓和熵。荧光测量(K(D) 0.45 microM)和ITC测量(K(D) 0.15 microM)均表明全铁frataxin与ISU形成具有亚微摩尔结合亲和力的复合物。重要的是,无辅基frataxin不与ISU结合,这表明铁在交联这两种蛋白质和/或稳定ISU识别的frataxin结构中起着重要作用。全铁frataxin还被证明能介导铁从全铁frataxin转移到ISU上[2Fe-2S]簇形成的成核位点。我们在其他地方已经证明[《美国化学会志》2002年,124卷,8774 - 8775页],这种与铁结合的ISU形式对于全铁ISU的组装是可行的,要么通过随后添加硫化物,要么通过NifS介导的硫传递。提供全铁frataxin和无机硫化物足以使簇组装产率高达70%。以NifS作为硫供体,获得了超过70%的全铁ISU产率。紫外可见光谱和圆二色光谱特征均与先前表征的ISU蛋白一致。在[2Fe-2S]簇组装反应过程中,通过形成的全铁ISU在456 nm处的吸光度监测簇组装的时间进程。在50 mM Tris-HCl(pH 7.5)和4.3 mM DTT条件下,用100 microM ISU、2.4 mM Na(2)S和40 microM全铁frataxin测定了动力学速率常数k(obs)约为0.075 min(-)(1)。对于NifS介导的硫传递也获得了相似的速率,这与frataxin中铁的释放作为簇组装反应中的限速步骤一致。