Understanding the Functional Properties of Lipid Heterogeneity in Pulmonary Surfactant Monolayers at the Atomistic Level

0535901 - ÚOCHB 2021 RIV CH eng J - Journal Article
Liekkinen, J. - de Santos Moreno, B. - Paananen, R. O. - Vattulainen, I. - Monticelli, L. - de la Serna, J. B. - Javanainen, Matti
Understanding the Functional Properties of Lipid Heterogeneity in Pulmonary Surfactant Monolayers at the Atomistic Level.
Frontiers in Cell and Developmental Biology. Roč. 8, Nov 16 (2020), č. článku 581016. ISSN 2296-634X. E-ISSN 2296-634X
Institutional support: RVO:61388963
Keywords : pulmonary surfactant * lipid monolayer * molecular dynamics simulation * pressure-area isotherm * atomic force microscopy * heterogeneity * membrane domain
OECD category: Physical chemistry
Impact factor: 6.684, year: 2020
Method of publishing: Open access
https://doi.org/10.3389/fcell.2020.581016

Pulmonary surfactant is a complex mixture of lipids and proteins lining the interior of the alveoli, and constitutes the first barrier to both oxygen and pathogens as they progress toward blood circulation. Despite decades of study, the behavior of the pulmonary surfactant at the molecular scale is poorly understood, which hinders the development of effective surfactant replacement therapies, useful in the treatment of several lung-related diseases. In this work, we combined all-atom molecular dynamics simulations, Langmuir trough measurements, and AFM imaging to study synthetic four-component lipid monolayers designed to model protein-free pulmonary surfactant. We characterized the structural and dynamic properties of the monolayers with a special focus on lateral heterogeneity. Remarkably, simulations reproduce almost quantitatively the experimental data on pressure-area isotherms and the presence of lateral heterogeneities highlighted by AFM. Quite surprisingly, the pressure-area isotherms do not show a plateau region, despite the presence of liquid-condensed nanometer-sized domains at surface pressures larger than 20 mN/m. In the simulations, the liquid-condensed domains were small and transient, but they did not coalesce to yield a separate phase. They were only slightly enriched in DPPC and cholesterol, and their chemical composition remained very similar to the overall composition of the monolayer membrane. Instead, they differed from liquid-expanded regions in terms of membrane thickness (in agreement with AFM data), diffusion rates, as well as acyl chain packing and orientation. We hypothesize that such lateral heterogeneities are crucial for lung surfactant function, as they allow both efficient packing, to achieve low surface tension, and sufficient fluidity, critical for rapid adsorption to the air–liquid interface during the breathing cycle.
Permanent Link: http://hdl.handle.net/11104/0313859