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Fluorescence resonance energy transfer analysis of protein translocase. SecYE from Thermus thermophilus HB8 forms a constitutive oligomer in membranes.
- Source :
-
The Journal of biological chemistry [J Biol Chem] 2003 Apr 18; Vol. 278 (16), pp. 14257-64. Date of Electronic Publication: 2003 Jan 17. - Publication Year :
- 2003
-
Abstract
- SecY and SecE are the two principal translocase subunits that create a channel-like pathway for the transit of preprotein across the bacterial cytoplasmic membrane. Here we report the cloning, expression, and purification of the SecYE complex (TSecYE) from a thermophilic bacterium, Thermus thermophilus HB8. Purified TSecYE can be reconstituted into proteoliposomes that function in T. thermophilus SecA (TSecA) dependent preprotein translocation. After the mixing of TSecYE derivatives labeled with either a donor or an acceptor fluorophore during reconstitution, fluorescence resonance energy transfer experiments demonstrated that 2 or more units of TSecYE in the lipid bilayer associate to form a largely non-exchangeable oligomeric structure.
- Subjects :
- Amino Acid Sequence
Cell Membrane metabolism
Cloning, Molecular
Escherichia coli Proteins metabolism
Fluorescence Resonance Energy Transfer
Fluorescent Dyes pharmacology
Lipid Bilayers metabolism
Liposomes metabolism
Molecular Sequence Data
Mutation
Plasmids metabolism
Protein Binding
Proteolipids metabolism
Rhodamines pharmacology
SEC Translocation Channels
Sequence Homology, Amino Acid
Spectrometry, Fluorescence
Escherichia coli Proteins chemistry
Thermus thermophilus enzymology
Subjects
Details
- Language :
- English
- ISSN :
- 0021-9258
- Volume :
- 278
- Issue :
- 16
- Database :
- MEDLINE
- Journal :
- The Journal of biological chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 12533543
- Full Text :
- https://doi.org/10.1074/jbc.M300230200