Decoupling of crystalline and conformational degrees of freedom in lipid monolayers

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Decoupling of crystalline and conformational degrees of freedom in lipid monolayers. / Ipsen, John Hjort; Mouritsen, Ole G.; Zuckermann, Martin J.

In: The Journal of Chemical Physics, Vol. 91, No. 3, 1989, p. 1855-1865.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Ipsen, JH, Mouritsen, OG & Zuckermann, MJ 1989, 'Decoupling of crystalline and conformational degrees of freedom in lipid monolayers', The Journal of Chemical Physics, vol. 91, no. 3, pp. 1855-1865. https://doi.org/10.1063/1.457090

APA

Ipsen, J. H., Mouritsen, O. G., & Zuckermann, M. J. (1989). Decoupling of crystalline and conformational degrees of freedom in lipid monolayers. The Journal of Chemical Physics, 91(3), 1855-1865. https://doi.org/10.1063/1.457090

Vancouver

Ipsen JH, Mouritsen OG, Zuckermann MJ. Decoupling of crystalline and conformational degrees of freedom in lipid monolayers. The Journal of Chemical Physics. 1989;91(3):1855-1865. https://doi.org/10.1063/1.457090

Author

Ipsen, John Hjort ; Mouritsen, Ole G. ; Zuckermann, Martin J. / Decoupling of crystalline and conformational degrees of freedom in lipid monolayers. In: The Journal of Chemical Physics. 1989 ; Vol. 91, No. 3. pp. 1855-1865.

Bibtex

@article{c12df12754aa464880aa6c6b8d4da1a8,
title = "Decoupling of crystalline and conformational degrees of freedom in lipid monolayers",
abstract = "A theoretical study is performed on a microscopic interaction model which describes the transitions between liquid and solid phases of lipid monolayers spread on air/water interfaces. The model accounts for condensation in terms of acyl-chain conformational degrees of freedom as well as in terms of variables which describe the orientations of crystalline domains in the solid. The phase behavior of the model as a function of temperature and lateral pressure is explored using mean-field theory and computer-simulation techniques. Attention is paid to the particular interplay between the two types of condensation processes and effects on the phase behavior due to decoupling of crystalline and conformational order parameters. In the case of decoupling, the model predicts that the high-pressure solid-conformationally ordered phase is separated from the low-pressure liquid-conformationally disordered phase by a liquid-conformationally ordered phase. This prediction is consistent with synchrotron x-ray experiments which show that the chain-ordering transition and the crystallization process need not take place at the same lateral pressure. A characterization is provided of the nonequilibrium effects and pattern-formation processes observed along the isotherms in the phase diagram spanned by lateral pressure and area. A description is given of the kinetics of the nonequilibrium phase transitions and the concomitant heterogeneous microstructure of the monolayer. This leads to an explanation of the peculiarities of the experimentally observed isotherms of lipid monolayer phase behavior. It is pointed out that cholesterol, which promotes lipid-chain conformational order, has a unique capacity of acting as a 'crystal breaker' in the solid monolayer phases and therefore provides a molecular mechanism for decoupling crystalline and conformational order in lipid monolayers containing cholesterol. The phase diagram of mixed cholesterol-lipid monolayers is derived and discussed in relation to monolayer experiments.",
author = "Ipsen, {John Hjort} and Mouritsen, {Ole G.} and Zuckermann, {Martin J.}",
year = "1989",
doi = "10.1063/1.457090",
language = "English",
volume = "91",
pages = "1855--1865",
journal = "The Journal of Chemical Physics",
issn = "0021-9606",
publisher = "American Institute of Physics",
number = "3",

}

RIS

TY - JOUR

T1 - Decoupling of crystalline and conformational degrees of freedom in lipid monolayers

AU - Ipsen, John Hjort

AU - Mouritsen, Ole G.

AU - Zuckermann, Martin J.

PY - 1989

Y1 - 1989

N2 - A theoretical study is performed on a microscopic interaction model which describes the transitions between liquid and solid phases of lipid monolayers spread on air/water interfaces. The model accounts for condensation in terms of acyl-chain conformational degrees of freedom as well as in terms of variables which describe the orientations of crystalline domains in the solid. The phase behavior of the model as a function of temperature and lateral pressure is explored using mean-field theory and computer-simulation techniques. Attention is paid to the particular interplay between the two types of condensation processes and effects on the phase behavior due to decoupling of crystalline and conformational order parameters. In the case of decoupling, the model predicts that the high-pressure solid-conformationally ordered phase is separated from the low-pressure liquid-conformationally disordered phase by a liquid-conformationally ordered phase. This prediction is consistent with synchrotron x-ray experiments which show that the chain-ordering transition and the crystallization process need not take place at the same lateral pressure. A characterization is provided of the nonequilibrium effects and pattern-formation processes observed along the isotherms in the phase diagram spanned by lateral pressure and area. A description is given of the kinetics of the nonequilibrium phase transitions and the concomitant heterogeneous microstructure of the monolayer. This leads to an explanation of the peculiarities of the experimentally observed isotherms of lipid monolayer phase behavior. It is pointed out that cholesterol, which promotes lipid-chain conformational order, has a unique capacity of acting as a 'crystal breaker' in the solid monolayer phases and therefore provides a molecular mechanism for decoupling crystalline and conformational order in lipid monolayers containing cholesterol. The phase diagram of mixed cholesterol-lipid monolayers is derived and discussed in relation to monolayer experiments.

AB - A theoretical study is performed on a microscopic interaction model which describes the transitions between liquid and solid phases of lipid monolayers spread on air/water interfaces. The model accounts for condensation in terms of acyl-chain conformational degrees of freedom as well as in terms of variables which describe the orientations of crystalline domains in the solid. The phase behavior of the model as a function of temperature and lateral pressure is explored using mean-field theory and computer-simulation techniques. Attention is paid to the particular interplay between the two types of condensation processes and effects on the phase behavior due to decoupling of crystalline and conformational order parameters. In the case of decoupling, the model predicts that the high-pressure solid-conformationally ordered phase is separated from the low-pressure liquid-conformationally disordered phase by a liquid-conformationally ordered phase. This prediction is consistent with synchrotron x-ray experiments which show that the chain-ordering transition and the crystallization process need not take place at the same lateral pressure. A characterization is provided of the nonequilibrium effects and pattern-formation processes observed along the isotherms in the phase diagram spanned by lateral pressure and area. A description is given of the kinetics of the nonequilibrium phase transitions and the concomitant heterogeneous microstructure of the monolayer. This leads to an explanation of the peculiarities of the experimentally observed isotherms of lipid monolayer phase behavior. It is pointed out that cholesterol, which promotes lipid-chain conformational order, has a unique capacity of acting as a 'crystal breaker' in the solid monolayer phases and therefore provides a molecular mechanism for decoupling crystalline and conformational order in lipid monolayers containing cholesterol. The phase diagram of mixed cholesterol-lipid monolayers is derived and discussed in relation to monolayer experiments.

U2 - 10.1063/1.457090

DO - 10.1063/1.457090

M3 - Journal article

AN - SCOPUS:0000835969

VL - 91

SP - 1855

EP - 1865

JO - The Journal of Chemical Physics

JF - The Journal of Chemical Physics

SN - 0021-9606

IS - 3

ER -

ID: 238390037