Membrane protein insertion through a mitochondrial β-barrel gate
Author(s) -
Alexandra I. C. Höhr,
Caroline Lindau,
Christophe Wirth,
Jian Qiu,
David A. Stroud,
Stephan Kutik,
Bernard Guiard,
Carola Hunte,
Thomas Becker,
Nikolaus Pfanner,
Nils Wiedemann
Publication year - 2018
Publication title -
science
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.aah6834
Subject(s) - bacterial outer membrane , barrel (horology) , membrane , microbiology and biotechnology , biogenesis , translocase of the inner membrane , membrane protein , translocase of the outer membrane , mitochondrial membrane transport protein , biophysics , outer membrane efflux proteins , transport protein , chemistry , biology , membrane transport protein , biochemistry , materials science , escherichia coli , composite material , gene
The biogenesis of mitochondria, chloroplasts, and Gram-negative bacteria requires the insertion of β-barrel proteins into the outer membranes. Homologous Omp85 proteins are essential for membrane insertion of β-barrel precursors. It is unknown if precursors are threaded through the Omp85-channel interior and exit laterally or if they are translocated into the membrane at the Omp85-lipid interface. We have mapped the interaction of a precursor in transit with the mitochondrial Omp85-channel Sam50 in the native membrane environment. The precursor is translocated into the channel interior, interacts with an internal loop, and inserts into the lateral gate by β-signal exchange. Transport through the Omp85-channel interior followed by release through the lateral gate into the lipid phase may represent a basic mechanism for membrane insertion of β-barrel proteins.
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