Frontiers in Cell and Developmental BiologyBiophysicsPeer-reviewed journal article
Understanding the Functional Properties of Lipid Heterogeneity in Pulmonary Surfactant Monolayers at the Atomistic Level
Juho Liekkinen, Berta de Santos Moreno, Riku O. Paananen, Ilpo Vattulainen, Luca Monticelli, Jorge Bernardino de la SernaiD, Matti JavanaineniD
Abstract
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 is poorly understood on the molecular scale, 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 domains were small and transient, but they did not coalesce to yield a separate phase. The liquid–condensed domains 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, 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.Competing Interest StatementThe authors have declared no competing interest.View Full Text
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Surfactant Proteins SP-B and SP-C in Pulmonary Surfactant Monolayers: Physical Properties Controlled by Specific Protein-Lipid Interactions
J. Liekkinen, A. Olzynska, … M. Javanainen·bioRxiv·Dec 12, 2022
- Subphase Material Stabilizes Films of Pulmonary Surfactant
K. Andreev, M. Martynowycz, … D. Gidalevitz·bioRxiv·Feb 27, 2020
- An image-based biophysical model of the lung to investigate the effect of pulmonary surfactant on lung function
Sunder Neelakantan, Kyle J. Myers, … Reza Avazmohammadi·bioRxiv·Feb 15, 2025
- Experiments and modelling of pulmonary surfactant disruption by aerosolised compounds
Helen Barlow, Sreyoshee Roy Sengupta, … Jorid Birkelund Sørli·Colloids and Surfaces B BiointerfacesPeer-reviewed·Dec 27, 2024
- Interplay Between Pulmonary Membrane Properties and Lung Disease: a Study of Seven Bottlenose Dolphins
Marilyn Porras-Gómez, Bengu Sueda Sengul, … Cecília Leal·bioRxiv·Oct 17, 2025
- Liquid foam therapy (LiFT) for homogenous distribution of exogenous pulmonary surfactant in ARDS
R. Fishler, Y. Ostrovski, … J. Sznitman·bioRxiv·Nov 30, 2020