Structure, Stability, and Hydration of a Polypeptide in AOT Reverse Micelles

In this communication, we provide theoretical evidence that the folded structure of a simple peptide, alanine zwitterionic octapeptide, or A8, unstable in solution, becomes stable in a reverse micelle (RM) of appropriate size. Our molecular dynamics simulations were carried out for realistic models...

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Veröffentlicht in:Journal of the American Chemical Society 2006-01, Vol.128 (2), p.382-383
Hauptverfasser: Abel, Stéphane, Waks, Marcel, Urbach, Wladimir, Marchi, Massimo
Format: Artikel
Sprache:eng
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Zusammenfassung:In this communication, we provide theoretical evidence that the folded structure of a simple peptide, alanine zwitterionic octapeptide, or A8, unstable in solution, becomes stable in a reverse micelle (RM) of appropriate size. Our molecular dynamics simulations were carried out for realistic models of sodium 2-ethylhexylsulfosuccinate RM in isooctane, simulated for an extended period of time. For the RM of the smaller size, we find that a helical structure is stable for the whole length of the simulation. On the contrary, the peptide very quickly takes an extended structure in larger micelles.
ISSN:0002-7863
1520-5126
DOI:10.1021/ja053043u