TY - JOUR
T1 - Interaction forces and membrane charge tunability
T2 - Oleic acid containing membranes in different pH conditions
AU - Kurniawan, James
AU - Suga, Keishi
AU - Kuhl, Tonya L.
N1 - Funding Information:
This work was primarily supported by the NSF chemistry division through grant CHE-1413745 . We thank Joao Ventrici for the assistance with atomic force microscopy. Keishi Suga expresses his gratitude for Engineering Science Young Researcher Dispatch Program and Multidisciplinary Research Laboratory System of Osaka University.
Publisher Copyright:
© 2016
PY - 2017/2/1
Y1 - 2017/2/1
N2 - Oleic acid is known to interact with saturated lipid molecules and increase the fluidity of gel phase lipid membranes. In this work, the thermodynamic properties of mixed monolayers of 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) and oleic acid at the air-water interface were determined using Langmuir isotherms. The isotherm study revealed an attractive interaction between oleic acid and DPPC. The incorporation of oleic acid also monotonically decreased the elastic modulus of the monolayer indicative of higher fluidity with increasing oleic acid content. Using the surface force apparatus, intermembrane force–distance profiles were obtained for substrate supported DPPC membranes containing 30 mol% oleic acid at pH 5.8 and 7.4. Three different preparation conditions resulted in distinct force profiles. Membranes prepared in pH 5.8 subphase had a low number of nanoscopic defects ≤ 1% and an adhesion magnitude of ~ 0.6 mN/m. A slightly higher defect density of 1–4% was found for membranes prepared in a physiological pH 7.4 subphase. The presence of the exposed hydrophobic moieties resulted in a higher adhesion magnitude of 2.9 mN/m. Importantly, at pH 7.4, some oleic acid deprotonates resulting in a long-range electrostatic repulsion. Even though oleic acid increased the DPPC bilayer fluidity and the number of defects, no membrane restructuring was observed indicating that the system maintained a stable configuration.
AB - Oleic acid is known to interact with saturated lipid molecules and increase the fluidity of gel phase lipid membranes. In this work, the thermodynamic properties of mixed monolayers of 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) and oleic acid at the air-water interface were determined using Langmuir isotherms. The isotherm study revealed an attractive interaction between oleic acid and DPPC. The incorporation of oleic acid also monotonically decreased the elastic modulus of the monolayer indicative of higher fluidity with increasing oleic acid content. Using the surface force apparatus, intermembrane force–distance profiles were obtained for substrate supported DPPC membranes containing 30 mol% oleic acid at pH 5.8 and 7.4. Three different preparation conditions resulted in distinct force profiles. Membranes prepared in pH 5.8 subphase had a low number of nanoscopic defects ≤ 1% and an adhesion magnitude of ~ 0.6 mN/m. A slightly higher defect density of 1–4% was found for membranes prepared in a physiological pH 7.4 subphase. The presence of the exposed hydrophobic moieties resulted in a higher adhesion magnitude of 2.9 mN/m. Importantly, at pH 7.4, some oleic acid deprotonates resulting in a long-range electrostatic repulsion. Even though oleic acid increased the DPPC bilayer fluidity and the number of defects, no membrane restructuring was observed indicating that the system maintained a stable configuration.
KW - DPPC
KW - Isotherm
KW - Oleic acid
KW - Protonation
KW - SFA
KW - Supported lipid bilayer
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U2 - 10.1016/j.bbamem.2016.11.001
DO - 10.1016/j.bbamem.2016.11.001
M3 - Article
C2 - 27823928
AN - SCOPUS:84997817435
SN - 0005-2736
VL - 1859
SP - 211
EP - 217
JO - Biochimica et Biophysica Acta - Biomembranes
JF - Biochimica et Biophysica Acta - Biomembranes
IS - 2
ER -