The recent Journal of General Physiology perpsectives on membrane protein insertion (129:351–377) covered many valuable strategies to examine how amino acid sequence determines protein insertion into membranes and the probability that sequences form transmembrane (TM) helices. Each approach described has unique advantages, and a complete exploration of this problem clearly requires combining approaches, including approaches not discussed in the perspectives, such as the use of synthetic hydrophobic helices inserted into model membrane vesicles. Using a diverse set of biophysical methods, several groups have used the latter approach to understand fundamental issues of membrane protein structure and function, including the configuration of membrane-inserted hydrophobic helices (TM or non-TM), the effect of hydrophobic helices on bilayer structure (and vice versa), and helix–helix interaction (Bechinger, 1996; Hunt et al., 1997; Ren et al., 1997, 1999; Killian, 1998; Webb et al.,...
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1 August 2007
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Letter to the Editor|
July 16 2007
Using Model Membrane-inserted Hydrophobic Helices to Study the Equilibrium between Transmembrane and Nontransmembrane States
Erwin London
Erwin London
Department of Biochemistry and Cell Biology, Stony Brook University, Stony Brook, NY 11794
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Erwin London
Department of Biochemistry and Cell Biology, Stony Brook University, Stony Brook, NY 11794
Correspondence to Erwin London: [email protected]
Abbreviation used in this paper: TM, transmembrane.
Online ISSN: 1540-7748
Print ISSN: 0022-1295
The Rockefeller University Press
2007
J Gen Physiol (2007) 130 (2): 229–232.
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Erwin London; Using Model Membrane-inserted Hydrophobic Helices to Study the Equilibrium between Transmembrane and Nontransmembrane States . J Gen Physiol 1 August 2007; 130 (2): 229–232. doi: https://doi.org/10.1085/jgp.200709842
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See also
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- Perspectives on Membrane Protein Insertion, Protein–Bilayer Interactions, and Amino Acid Side Hydrophobicity
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