Author:
Martincová Eva,Voleman Luboš,Pyrih Jan,Žárský Vojtěch,Vondráčková Pavlína,Kolísko Martin,Tachezy Jan,Doležal Pavel
Abstract
Giardia intestinalisparasites contain mitosomes, one of the simplest mitochondrion-related organelles. Strategies to identify the functions of mitosomes have been limited mainly to homology detection, which is not suitable for identifying species-specific proteins and their functions. Anin vivoenzymatic tagging technique based on theEscherichia colibiotin ligase (BirA) has been introduced toG. intestinalis; this method allows for the compartment-specific biotinylation of a protein of interest. Known proteins involved in the mitosomal protein import werein vivotagged, cross-linked, and used to copurify complexes from the outer and inner mitosomal membranes in a single step. New proteins were then identified by mass spectrometry. This approach enabled the identification of highly diverged mitosomal Tim44 (GiTim44), the first known component of the mitosomal inner membrane translocase (TIM). In addition, our subsequent bioinformatics searches returned novel diverged Tim44 paralogs, which mediate the translation and mitosomal insertion of mitochondrially encoded proteins in other eukaryotes. However, most of the identified proteins are specific toG. intestinalisand even absent from the related diplomonad parasiteSpironucleus salmonicida, thus reflecting the unique character of the mitosomal metabolism. Thein vivoenzymatic tagging also showed that proteins enter the mitosome posttranslationally in an unfolded state and without vesicular transport.
Publisher
American Society for Microbiology
Subject
Cell Biology,Molecular Biology
Cited by
41 articles.
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