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Membrane protein folding: beyond the two stage model.
- Source :
-
FEBS letters [FEBS Lett] 2003 Nov 27; Vol. 555 (1), pp. 122-5. - Publication Year :
- 2003
-
Abstract
- The folding of alpha-helical membrane proteins has previously been described using the two stage model, in which the membrane insertion of independently stable alpha-helices is followed by their mutual interactions within the membrane to give higher order folding and oligomerization. Given recent advances in our understanding of membrane protein structure it has become apparent that in some cases the model may not fully represent the folding process. Here we present a three stage model which gives considerations to ligand binding, folding of extramembranous loops, insertion of peripheral domains and the formation of quaternary structure.
- Subjects :
- Aquaporins chemistry
Bacterial Proteins chemistry
Bacteriorhodopsins chemistry
Binding Sites
Escherichia coli Proteins chemistry
Ligands
Lipid Bilayers chemistry
Models, Molecular
Potassium Channels chemistry
Protein Folding
Protein Structure, Quaternary
Protein Structure, Secondary
Protein Structure, Tertiary
Thermodynamics
Membrane Proteins chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 0014-5793
- Volume :
- 555
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- FEBS letters
- Publication Type :
- Academic Journal
- Accession number :
- 14630331
- Full Text :
- https://doi.org/10.1016/s0014-5793(03)01106-2