Effects of Divalent Cations on Phase Behavior and Structure of a Zwitterionic Phospholipid (DMPC) Mono layer at the Air-Water Interface

被引:46
作者
Kewalramani, Sumit [1 ]
Hlaing, Htay [1 ,2 ]
Ocko, Benjamin M. [1 ]
Kuzmenko, Ivan [3 ]
Fukuto, Masafumi [1 ]
机构
[1] Brookhaven Natl Lab, Condensed Matter Phys & Mat Sci Dept, Upton, NY 11973 USA
[2] SUNY Stony Brook, Dept Phys & Astron, Stony Brook, NY 11794 USA
[3] Argonne Natl Lab, Adv Photon Source, Xray Sci Div, Argonne, IL 60439 USA
关键词
PHOSPHATIDYLCHOLINE BILAYER-MEMBRANES; LANGMUIR MONOLAYERS; METAL-CATIONS; IONS; FILMS; TRANSITIONS; ADSORPTION; BINDING; ANIONS;
D O I
10.1021/jz9002873
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Effects of divalent cations (Ca2+, Mg2+, Ni2+ and Zn2+) on a zwitter-ionic phospholipid monolayer at the air-water interface are investigated by surface pressure-area isotherms and in situ X-rays scattering. Divalent cations lower the surface pressure for the fluid (LE) to condensed (L-2) phase transition in a strongly ion-specific manner. Surprisingly, the two-dimensional lattice dimensions and the tilt of the lipids' alkyl tails in the L-2 phase show a nearly ion-nonspecific dependence on the excess surface pressure above the transition pressure. "An empirical universal" relationship was found between the tail tilt and the excess pressure, with the tails in the L-2 phase always displaying a tilt of 29 degrees at the transition. A practical implication of these results is that regardless of the divalent cation present, the microscopic details of the lipid tail packing in the L-2 phase can be deduced at any surface pressure once the transition pressure is obtained from isotherms.
引用
收藏
页码:489 / 495
页数:7
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