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寄生虫原生动物布氏锥虫的综合亚线粒体蛋白质图谱定义了细胞器生物学的关键特征。

Comprehensive sub-mitochondrial protein map of the parasitic protist Trypanosoma brucei defines critical features of organellar biology.

机构信息

Institute of Parasitology, Biology Centre, Czech Academy of Sciences, České Budějovice (Budweis), Czech Republic; Department of Biochemistry, University of Cambridge, Cambridge, UK; Faculty of Science, University of Ostrava, Ostrava, Czech Republic.

Institute of Parasitology, Biology Centre, Czech Academy of Sciences, České Budějovice (Budweis), Czech Republic.

出版信息

Cell Rep. 2023 Sep 26;42(9):113083. doi: 10.1016/j.celrep.2023.113083. Epub 2023 Sep 4.

DOI:10.1016/j.celrep.2023.113083
PMID:37669165
Abstract

We have generated a high-confidence mitochondrial proteome (MitoTag) of the Trypanosoma brucei procyclic stage containing 1,239 proteins. For 337 of these, a mitochondrial localization had not been described before. We use the TrypTag dataset as a foundation and take advantage of the properties of the fluorescent protein tag that causes aberrant but fortuitous accumulation of tagged matrix and inner membrane proteins near the kinetoplast (mitochondrial DNA). Combined with transmembrane domain predictions, this characteristic allowed categorization of 1,053 proteins into mitochondrial sub-compartments, the detection of unique matrix-localized fucose and methionine synthesis, and the identification of new kinetoplast proteins, which showed kinetoplast-linked pyrimidine synthesis. Moreover, disruption of targeting signals by tagging allowed mapping of the mode of protein targeting to these sub-compartments, identifying a set of C-tail anchored outer mitochondrial membrane proteins and mitochondrial carriers likely employing multiple target peptides. This dataset represents a comprehensive, updated mapping of the mitochondrion.

摘要

我们已经生成了一份高可信度的布鲁氏锥虫前鞭毛体的线粒体蛋白质组(MitoTag),其中包含 1239 种蛋白质。对于其中的 337 种蛋白质,以前没有描述过它们的线粒体定位。我们利用 TrypTag 数据集作为基础,并利用荧光蛋白标签的特性,该特性导致标记的基质和内膜蛋白在动基体(线粒体 DNA)附近异常但偶然地积累。结合跨膜结构域预测,这一特征将 1053 种蛋白质分类到线粒体亚区室中,检测到独特的基质定位的岩藻糖和蛋氨酸合成,并鉴定了新的动基体蛋白,它们显示出与动基体相连的嘧啶合成。此外,通过标记破坏靶向信号允许将蛋白质靶向这些亚区室的模式进行映射,确定了一组可能使用多个靶向肽的 C 端锚定在外膜蛋白和线粒体载体。这个数据集代表了对线粒体的全面、更新的映射。

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