Your browser doesn't support javascript.
loading
n-Alcohol Length Governs Shift in Lo-Ld Mixing Temperatures in Synthetic and Cell-Derived Membranes.
Cornell, Caitlin E; McCarthy, Nicola L C; Levental, Kandice R; Levental, Ilya; Brooks, Nicholas J; Keller, Sarah L.
Afiliação
  • Cornell CE; University of Washington, Department of Chemistry, Seattle, Washington.
  • McCarthy NLC; Department of Chemistry, Imperial College London, London, United Kingdom.
  • Levental KR; Department of Integrative Biology and Pharmacology, McGovern Medical School at The University of Texas Medical Center, Houston, Texas.
  • Levental I; Department of Integrative Biology and Pharmacology, McGovern Medical School at The University of Texas Medical Center, Houston, Texas.
  • Brooks NJ; Department of Chemistry, Imperial College London, London, United Kingdom.
  • Keller SL; University of Washington, Department of Chemistry, Seattle, Washington. Electronic address: slkeller@chem.washington.edu.
Biophys J ; 113(6): 1200-1211, 2017 Sep 19.
Article em En | MEDLINE | ID: mdl-28801104
ABSTRACT
A persistent challenge in membrane biophysics has been to quantitatively predict how membrane physical properties change upon addition of new amphiphiles (e.g., lipids, alcohols, peptides, or proteins) in order to assess whether the changes are large enough to plausibly result in biological ramifications. Because of their roles as general anesthetics, n-alcohols are perhaps the best-studied amphiphiles of this class. When n-alcohols are added to model and cell membranes, changes in membrane parameters tend to be modest. One striking exception is found in the large decrease in liquid-liquid miscibility transition temperatures (Tmix) observed when short-chain n-alcohols are incorporated into giant plasma membrane vesicles (GPMVs). Coexisting liquid-ordered and liquid-disordered phases are observed at temperatures below Tmix in GPMVs as well as in giant unilamellar vesicles (GUVs) composed of ternary mixtures of a lipid with a low melting temperature, a lipid with a high melting temperature, and cholesterol. Here, we find that when GUVs of canonical ternary mixtures are formed in aqueous solutions of short-chain n-alcohols (n ≤ 10), Tmix increases relative to GUVs in water. This shift is in the opposite direction from that reported for cell-derived GPMVs. The increase in Tmix is robust across GUVs of several types of lipids, ratios of lipids, types of short-chain n-alcohols, and concentrations of n-alcohols. However, as chain lengths of n-alcohols increase, nonmonotonic shifts in Tmix are observed. Alcohols with chain lengths of 10-14 carbons decrease Tmix in ternary GUVs of dioleoyl-PC/dipalmitoyl-PC/cholesterol, whereas 16 carbons increase Tmix again. Gray et al. observed a similar influence of the length of n-alcohols on the direction of the shift in Tmix. These results are consistent with a scenario in which the relative partitioning of n-alcohols between liquid-ordered and liquid-disordered phases evolves as the chain length of the n-alcohol increases.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Membrana Celular / Temperatura de Transição / Álcoois / Lipossomas Unilamelares Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Membrana Celular / Temperatura de Transição / Álcoois / Lipossomas Unilamelares Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2017 Tipo de documento: Article