Abstract
Mitochondria contain the translocator of the outer mitochondrial membrane (TOM) for protein entry into the organelle, and its subunit Tom40 forms a protein-conducting channel. Here we report the role of Tom40 in protein translocation across the membrane. The site-specific photocrosslinking experiment revealed that translocating unfolded or loosely folded precursor segments of up to 90 residues can be associated with Tom40. Purified Tom40 bound to non-native proteins and suppressed their aggregation when they are prone to aggregate. A denatured protein bound to the Tom40 channel blocked the protein import into mitochondria. These results indicate that, in contrast to the nonstick tunnel of the ribosome for polypeptide exit, the Tom40 channel offers an optimized environment to translocating non-native precursor proteins by preventing their aggregation.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Cloning, Molecular
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Intracellular Membranes / metabolism
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Kinetics
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L-Lactate Dehydrogenase (Cytochrome) / chemistry
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L-Lactate Dehydrogenase (Cytochrome) / metabolism
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Membrane Transport Proteins / chemistry
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Membrane Transport Proteins / metabolism*
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Mitochondria / metabolism
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Mitochondrial Membrane Transport Proteins
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Mitochondrial Proteins / chemistry*
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Mitochondrial Proteins / metabolism*
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Protein Conformation
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Protein Denaturation
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Protein Transport
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Recombinant Fusion Proteins / metabolism
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Recombinant Proteins / metabolism
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Saccharomyces cerevisiae Proteins / chemistry
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Saccharomyces cerevisiae Proteins / metabolism*
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Tetrahydrofolate Dehydrogenase / chemistry
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Tetrahydrofolate Dehydrogenase / metabolism
Substances
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Membrane Transport Proteins
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Mitochondrial Membrane Transport Proteins
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Mitochondrial Proteins
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Recombinant Fusion Proteins
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Recombinant Proteins
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Saccharomyces cerevisiae Proteins
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Tom40 protein, S cerevisiae
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L-Lactate Dehydrogenase (Cytochrome)
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Tetrahydrofolate Dehydrogenase