Characterisation of Tat protein transport complexes carrying inactivating mutations

Christopher A. McDevitt, Matthew G. Hicks, Tracy Palmer, Ben C. Berks

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    29 Citations (Scopus)

    Abstract

    The Tat system functions to transport folded proteins across the bacterial cytoplasmic membrane and the thylakoid membrane of plant chloroplasts. Tat transport involves a high molecular weight TatBC-containing complex that transiently associates with TatA during protein translocation. Sedimentation equilibrium experiments were used to determine a protein-only molecular mass for the TatBC complex of 630 +/- 30 kDa, suggesting that it contains approximately 13 copies of the TatB and TatC protomers. Point mutations that inactivate Tat transport have previously been identified in each of TatA, TatB, and TatC. Analysis of the TatBC complexes formed by these inactive variants demonstrates that the amino acid substitutions neither affect the composition of the TatBC complex nor cause accumulation of the assembled TatABC translocation site. In addition, the TatA protein is shown not to be required for the assembly or stability of the TatBC complex. (c) 2005 Elsevier Inc. All rights reserved.

    Original languageEnglish
    Pages (from-to)693-698
    Number of pages6
    JournalBiochemical and Biophysical Research Communications
    Volume329
    Issue number2
    DOIs
    Publication statusPublished - 2005

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