Olczak T, Dixon D W, Genco C A
Department of Medicine, Section of Infectious Diseases, Boston University School of Medicine, Boston, Massachusetts 02118, USA.
J Bacteriol. 2001 Oct;183(19):5599-608. doi: 10.1128/JB.183.19.5599-5608.2001.
Previous genetic and biochemical studies have confirmed that hemoglobin and hemin utilization in Porphyromonas gingivalis is mediated by the outer membrane hemoglobin and heme receptor HmuR, as well as gingipain K (Kgp), a lysine-specific cysteine protease, and gingipain R1 (HRgpA), one of two arginine-specific cysteine proteases. In this study we report on the binding specificity of the recombinant P. gingivalis HmuR protein and native gingipains for hemoglobin, hemin, various porphyrins, and metalloporphyrins as assessed by spectrophotometric assays, by affinity chromatography, and by enzyme-linked immunosorbent assay. Protoporphyrin, mesoporphyrin, deuteroporphyrin, hematoporphyrin, and some of their iron, copper, and zinc derivatives were examined to evaluate the role of both the central metal ion and the peripheral substituents on binding to recombinant HmuR and soluble gingipains. Scatchard analysis of hemin binding to Escherichia coli cells expressing recombinant membrane-associated six-His-tagged HmuR yielded a linear plot with a binding affinity of 2.4 x 10(-5) M. Recombinant E. coli cells bound the iron, copper, and zinc derivatives of protoporphyrin IX (PPIX) with similar affinities, and approximately four times more tightly than PPIX itself, which suggests that the active site of HmuR contains a histidine that binds the metal ion in the porphyrin ring. Furthermore, we found that recombinant HmuR prefers the ethyl and vinyl side chains of the PPIX molecule to either the larger hydroxyethyl or smaller hydrogen side chains. Kgp and HRgpA were demonstrated to bind various porphyrins and metalloporphyrins with affinities similar to those for hemin, indicating that the binding of Kgp and HRgpA to these porphyrins does not require a metal within the porphyrin ring. We did not detect the binding of RgpB, the arginine-specific cysteine protease that lacks a C-terminal hemagglutinin domain, to hemoglobin, porphyrins, or metalloporphyrins. Kgp and HRgpA, but not RgpB, were demonstrated to bind directly to soluble recombinant six-His-tagged HmuR. Several possible mechanisms for the cooperation between outer membrane receptor HmuR and proteases Kgp and HRgpA in hemin and hemoglobin binding and utilization are discussed.
先前的遗传学和生物化学研究证实,牙龈卟啉单胞菌中血红蛋白和血红素的利用是由外膜血红蛋白和血红素受体HmuR、赖氨酸特异性半胱氨酸蛋白酶牙龈蛋白酶K(Kgp)以及两种精氨酸特异性半胱氨酸蛋白酶之一的牙龈蛋白酶R1(HRgpA)介导的。在本研究中,我们报告了重组牙龈卟啉单胞菌HmuR蛋白和天然牙龈蛋白酶对血红蛋白、血红素、各种卟啉和金属卟啉的结合特异性,这些特异性通过分光光度法测定、亲和色谱法和酶联免疫吸附测定进行评估。对原卟啉、中卟啉、次卟啉、血卟啉及其一些铁、铜和锌衍生物进行了检测,以评估中心金属离子和周边取代基在与重组HmuR和可溶性牙龈蛋白酶结合中的作用。对血红素与表达重组膜相关六组氨酸标签HmuR的大肠杆菌细胞的结合进行Scatchard分析,得到一条线性图,结合亲和力为2.4×10⁻⁵M。重组大肠杆菌细胞以相似的亲和力结合原卟啉IX(PPIX)的铁、铜和锌衍生物,且结合紧密程度约为PPIX本身的四倍,这表明HmuR的活性位点含有一个与卟啉环中的金属离子结合的组氨酸。此外,我们发现重组HmuR更喜欢PPIX分子的乙基和乙烯基侧链,而不是更大的羟乙基或更小的氢侧链。已证明Kgp和HRgpA以与血红素相似的亲和力结合各种卟啉和金属卟啉,这表明Kgp和HRgpA与这些卟啉的结合不需要卟啉环内的金属。我们未检测到缺乏C末端血凝素结构域的精氨酸特异性半胱氨酸蛋白酶RgpB与血红蛋白、卟啉或金属卟啉的结合。已证明Kgp和HRgpA而非RgpB直接结合可溶性重组六组氨酸标签HmuR。讨论了外膜受体HmuR与蛋白酶Kgp和HRgpA在血红素和血红蛋白结合及利用中协同作用的几种可能机制。