Verissimo Andreia F, Shroff Namita P, Daldal Fevzi
From the Department of Biology, University of Pennsylvania, Philadelphia, Pennsylvania 19104-6019.
From the Department of Biology, University of Pennsylvania, Philadelphia, Pennsylvania 19104-6019
J Biol Chem. 2015 Jul 3;290(27):16989-7003. doi: 10.1074/jbc.M115.652818. Epub 2015 May 15.
The c-type cytochromes are electron transfer proteins involved in energy transduction. They have heme-binding (CXXCH) sites that covalently ligate heme b via thioether bonds and are classified into different classes based on their protein folds and the locations and properties of their cofactors. Rhodobacter capsulatus produces various c-type cytochromes using the cytochrome c maturation (Ccm) System I, formed from the CcmABCDEFGHI proteins. CcmI, a component of the heme ligation complex CcmFHI, interacts with the heme-handling protein CcmE and chaperones apocytochrome c2 by binding its C-terminal helix. Whether CcmI also chaperones other c-type apocytochromes, and the effects of heme on these interactions were unknown previously. Here, we purified different classes of soluble and membrane-bound c-type apocytochromes (class I, c2 and c1, and class II c') and investigated their interactions with CcmI and apoCcmE. We report that, in the absence of heme, CcmI and apoCcmE recognized different classes of c-type apocytochromes with different affinities (nM to μM KD values). When present, heme induced conformational changes in class I apocytochromes (e.g. c2) and decreased significantly their high affinity for CcmI. Knowing that CcmI does not interact with mature cytochrome c2 and that heme converts apocytochrome c2 into its b-type derivative, these findings indicate that CcmI holds the class I apocytochromes (e.g. c2) tightly until their noncovalent heme-containing b-type cytochrome-like intermediates are formed. We propose that these intermediates are subsequently converted into mature cytochromes following the covalent ligation of heme via the remaining components of the Ccm complex.
c型细胞色素是参与能量转导的电子传递蛋白。它们具有血红素结合(CXXCH)位点,通过硫醚键与血红素b共价连接,并根据其蛋白质折叠以及辅因子的位置和性质分为不同类别。荚膜红细菌利用由CcmABCDEFGHI蛋白形成的细胞色素c成熟(Ccm)系统I产生各种c型细胞色素。CcmI是血红素连接复合物CcmFHI的一个组成部分,与血红素处理蛋白CcmE相互作用,并通过结合其C端螺旋伴侣脱辅基细胞色素c2。此前尚不清楚CcmI是否也伴侣其他c型脱辅基细胞色素,以及血红素对这些相互作用的影响。在这里,我们纯化了不同类别的可溶性和膜结合c型脱辅基细胞色素(I类,c2和c1,以及II类c'),并研究了它们与CcmI和脱辅基CcmE的相互作用。我们报告称,在没有血红素的情况下,CcmI和脱辅基CcmE以不同亲和力(nM至μM KD值)识别不同类别的c型脱辅基细胞色素。当存在血红素时,它会诱导I类脱辅基细胞色素(如c2)的构象变化,并显著降低它们对CcmI的高亲和力。鉴于CcmI不与成熟的细胞色素c2相互作用,且血红素将脱辅基细胞色素c2转化为其b型衍生物,这些发现表明CcmI紧紧抓住I类脱辅基细胞色素(如c2),直到形成其含血红素的非共价b型细胞色素样中间体。我们提出,这些中间体随后通过Ccm复合物的其余组分在血红素的共价连接后转化为成熟的细胞色素。