Yokoyama Kohei, Gillespie John R, Van Voorhis Wesley C, Buckner Frederick S, Gelb Michael H
Department of Chemistry, University of Washington, Seattle, WA 98195, USA.
Mol Biochem Parasitol. 2008 Jan;157(1):32-43. doi: 10.1016/j.molbiopara.2007.09.006. Epub 2007 Oct 2.
Protein geranylgeranyltransferase type I (PGGT-I) and protein farnesyltransferase (PFT) occur in many eukaryotic cells. Both consist of two subunits, the common alpha subunit and a distinct beta subunit. In the gene database of protozoa Trypanosoma cruzi, the causative agent of Chagas' disease, a putative protein that consists of 401 amino acids with approximately 20% amino acid sequence identity to the PGGT-I beta of other species was identified, cloned, and characterized. Multiple sequence alignments show that the T. cruzi ortholog contains all three of the zinc-binding residues and several residues uniquely conserved in the beta subunit of PGGT-I. Co-expression of this protein and the alpha subunit of T. cruzi PFT in Sf9 insect cells yielded a dimeric protein that forms a tight complex selectively with [(3)H]geranylgeranyl pyrophosphate, indicating a key characteristic of a functional PGGT-I. Recombinant T. cruzi PGGT-I ortholog showed geranylgeranyltransferase activity with distinct specificity toward the C-terminal CaaX motif of protein substrates compared to that of the mammalian PGGT-I and T. cruzi PFT. Most of the CaaX-containing proteins with X=Leu are good substrates of T. cruzi PGGT-I, and those with X=Met are substrates for both T. cruzi PFT and PGGT-I, whereas unlike mammalian PGGT-I, those with X=Phe are poor substrates for T. cruzi PGGT-I. Several candidates for T. cruzi PGGT-I or PFT substrates containing the C-terminal CaaX motif are found in the T. cruzi gene database. Among five C-terminal peptides of those tested, a peptide of a Ras-like protein ending with CVLL was selectively geranylgeranylated by T. cruzi PGGT-I. Other peptides with CTQQ (Tcj2 DNAJ protein), CAVM (TcPRL-1 protein tyrosine phosphatase), CHFM (a small GTPase like protein), and CQLF (TcRho1 GTPase) were specific substrates for T. cruzi PFT but not for PGGT-I. The mRNA and protein of the T. cruzi PGGT-I beta ortholog were detected in three life-cycle stages of T. cruzi. Cytosol fractions from trypomastigotes (infectious mammalian stage) and epimastigotes (insect stage) were shown to contain levels of PGGT-I activity that are approximately 100-fold lower than PFT activity. The CaaX mimetics known as PGGT-I inhibitors show very low potency against T. cruzi PGGT-I compared to the mammalian enzyme, suggesting the potential to develop selective inhibitors against the parasite enzyme.
I型蛋白质香叶基香叶基转移酶(PGGT-I)和蛋白质法尼基转移酶(PFT)存在于许多真核细胞中。两者都由两个亚基组成,即共同的α亚基和一个独特的β亚基。在恰加斯病的病原体——原生动物克氏锥虫的基因数据库中,鉴定、克隆并表征了一种推定蛋白质,该蛋白质由401个氨基酸组成,与其他物种的PGGT-Iβ的氨基酸序列同一性约为20%。多序列比对表明,克氏锥虫的直系同源物包含所有三个锌结合残基以及在PGGT-Iβ亚基中独特保守的几个残基。该蛋白质与克氏锥虫PFT的α亚基在Sf9昆虫细胞中共表达产生了一种二聚体蛋白质,该二聚体蛋白质与[³H]香叶基香叶基焦磷酸选择性形成紧密复合物,表明其具有功能性PGGT-I的关键特征。与哺乳动物PGGT-I和克氏锥虫PFT相比,重组克氏锥虫PGGT-I直系同源物对蛋白质底物的C末端CaaX基序具有独特的香叶基香叶基转移酶活性。大多数X为Leu的含CaaX蛋白质是克氏锥虫PGGT-I的良好底物,而X为Met的那些蛋白质是克氏锥虫PFT和PGGT-I的底物,与哺乳动物PGGT-I不同的是,X为Phe的那些蛋白质是克氏锥虫PGGT-I的不良底物。在克氏锥虫基因数据库中发现了几种含有C末端CaaX基序的克氏锥虫PGGT-I或PFT底物候选物。在测试的五个C末端肽中,一种以CVLL结尾的类Ras蛋白的肽被克氏锥虫PGGT-I选择性地香叶基香叶基化。其他含有CTQQ(Tcj2 DNAJ蛋白)、CAVM(TcPRL-1蛋白酪氨酸磷酸酶)、CHFM(一种类小GTP酶蛋白)和CQLF(TcRho1 GTP酶)的肽是克氏锥虫PFT的特异性底物,而不是PGGT-I的底物。在克氏锥虫的三个生命周期阶段检测到了克氏锥虫PGGT-Iβ直系同源物的mRNA和蛋白质。来自锥鞭毛体(感染性哺乳动物阶段)和无鞭毛体(昆虫阶段)的胞质部分显示PGGT-I活性水平比PFT活性低约100倍。与哺乳动物酶相比,被称为PGGT-I抑制剂的CaaX模拟物对克氏锥虫PGGT-I的效力非常低,这表明有开发针对该寄生虫酶的选择性抑制剂的潜力。