Goldberg B, Yarlett N, Rattendi D, Lloyd D, Bacchi C J
Department of Chemistry and Physical Sciences, Pace University, New York, New York 10038, USA.
J Eukaryot Microbiol. 1997 Jul-Aug;44(4):345-51. doi: 10.1111/j.1550-7408.1997.tb05676.x.
The fate of the [methyl-14C] group of S-adenosylmethionine (AdoMet) in bloodstream forms of Trypanosoma brucei brucei, was studied. Trypanosomes were incubated with either [methyl-14C]methionine, [U-14C]methionine, S-[methyl-14C]AdoMet or [33S]methionine and incorporation into the total TCA precipitable fractions was followed. Incorporation of label into protein through methylation was estimated by comparing molar incorporation of [methyl-14C] and [U-14C]methionine to [35S]methionine. After 4-h incubation with [U-14C]methionine, [methyl-14C]methionine or [35S]methionine, cells incorporated label at mean rates of 2,880 pmol, 1,305 pmol and 296 pmol per mg total cellular protein, respectively. Cells incubated with [U-14C] or [methyl-14C]methionine in the presence of cycloheximide (50 micrograms/ml) for four hours incorporated label eight- and twofold more rapidly, respectively, than cells incubated with [35S]methionine and cycloheximide. [Methyl-14C] and [U-14C]methionine incorporation were > 85% decreased by co-incubation with unlabeled AdoMet (1 mM). The level of protein methylation remaining after 4-h treatment with cycloheximide was also inhibited with unlabeled AdoMet. The acid precipitable label from [U-14C]methionine incorporation was not appreciably hydrolyzed by DNAse or RNAse treatment but was 95% solubilized by proteinase K. [U-14C]methionine incorporated into the TCA precipitable fraction was susceptible to alkaline borate treatment, indicating that much of this label (55%) was incorporated as carboxymethyl groups. The rate of total lipid methylation was found to be 1.5 times that of protein methylation by incubating cells with [U-14C]methionine for six hours and differential extraction of the TCA lysate. These studies show T. b. brucei maintains rapid lipid and protein methylation, confirming previous studies demonstrating rapid conversion of methionine to AdoMet and subsequent production of post-methylation products of AdoMet in African trypanosomes.
研究了布氏布氏锥虫血流形式中S-腺苷甲硫氨酸(AdoMet)的[甲基-14C]基团的命运。将锥虫与[甲基-14C]甲硫氨酸、[U-14C]甲硫氨酸、S-[甲基-14C]AdoMet或[33S]甲硫氨酸一起孵育,并跟踪其掺入总三氯乙酸可沉淀部分的情况。通过比较[甲基-14C]和[U-14C]甲硫氨酸与[35S]甲硫氨酸的摩尔掺入量来估计通过甲基化掺入蛋白质中的标记物。用[U-14C]甲硫氨酸、[甲基-14C]甲硫氨酸或[35S]甲硫氨酸孵育4小时后,细胞掺入标记物的平均速率分别为每毫克总细胞蛋白2,880皮摩尔、1,305皮摩尔和296皮摩尔。在放线菌酮(50微克/毫升)存在下,用[U-14C]或[甲基-14C]甲硫氨酸孵育细胞4小时,其掺入标记物的速度分别比用[35S]甲硫氨酸和放线菌酮孵育的细胞快8倍和2倍。与未标记的AdoMet(1毫摩尔)共同孵育可使[甲基-14C]和[U-14C]甲硫氨酸的掺入量减少>85%。用放线菌酮处理4小时后剩余的蛋白质甲基化水平也受到未标记的AdoMet的抑制。[U-14C]甲硫氨酸掺入产生的酸可沉淀标记物经DNA酶或RNA酶处理后没有明显水解,但经蛋白酶K处理后95%可溶解。掺入三氯乙酸可沉淀部分的[U-14C]甲硫氨酸易受碱性硼酸盐处理的影响,这表明该标记物的大部分(55%)是以羧甲基基团的形式掺入的。通过用[U-14C]甲硫氨酸孵育细胞6小时并对三氯乙酸裂解物进行差异提取,发现总脂质甲基化速率是蛋白质甲基化速率的1.5倍。这些研究表明布氏布氏锥虫维持快速的脂质和蛋白质甲基化,证实了先前的研究,即证明非洲锥虫中甲硫氨酸快速转化为AdoMet以及随后产生AdoMet的甲基化后产物。