Published in Langmuir (ACS Publication): Enthalpic Effects of Chain Length and Unsaturation on Water Permeability Across Droplet Bilayers of Homologous Monoglycerides

Sunghee Lee, Ph.D. • January 23, 2017

Dr. Lee’s recent paper, titled “Enthalpic Effects of Chain Length and Unsaturation on Water Permeability Across Droplet Bilayers of Homologous Monoglycerides” has been published in Langmuir, a publication of the American Chemical Society.

The paper is coauthored by three undergraduates, Maria Lopez (’17 Biochemistry), Sue Ellen Evanglista (’17 Chemistry), and Melissa Morales (’16 Chemistry). In this paper, a deeper understanding of unassisted passive transport of water permeation across lipid membranes was attained by studies using a droplet interface bilayer (DIB) formed by the contact of two aqueous droplets in an immiscible solvent containing bilayer-forming surfactant. We have investigated the effect of acyl chain structure of amphiphilic monoglycerides on the osmotic permeability of water across DIB membranes composed of these monoglycerides, where the acyl chain length (C14 to C24), number of double bonds (1–4), and the position of double bond are varied systematically along the acyl chains. Both permeability values and activation energies have been extracted for water transport across a lipid bilayer formed of a homologous series of lipids, allowing us to make ready comparisons between the different lipids and potentially better elucidate the contributions that molecular motifs make to the permeation process. Congratulations to the research team!

Exploring Graphene Oxide–Cholesterol Interactions Across Model Membranes

By Sunghee Lee • February 23, 2026
We’re pleased to announce our new collaborative publication, “Study of the Interaction Between Graphene Oxide and Cholesterol Using Different Artificial Membrane Models,” conducted in partnership with colleagues in Italy. This work investigates how graphene oxide—an emerging nanomaterial with biomedical promise—interacts with cholesterol within lipid membranes. By employing various artificial membrane systems, we examined how membrane composition and organization influence these interactions, revealing key insights into the physicochemical mechanisms at play. Our results contribute to a deeper understanding of how nanomaterials engage with biological membranes, providing valuable guidance for the safe and effective design of graphene-based biomedical applications. Congratulations to all team members and our Italian collaborators on this exciting achievement! The full article is available here: https://www.sciencedirect.com/science/article/pii/S0021979726002821 .

New Insights into Serotonin’s Relationship with Cell Membranes

By Sunghee Lee • February 23, 2026
In this study, we explored how the membrane environment shapes the behavior of serotonin, a key neurotransmitter involved in mood regulation and neural signaling. By systematically varying lipid composition in model membranes, we uncovered how differences in lipid charge, fluidity, and packing influence serotonin’s nonspecific interactions with bilayers. Our findings shed new light on the physical chemistry of neurotransmitter–membrane interactions, with potential implications for understanding serotonin’s diverse physiological functions and its role in receptor signaling. Congratulations to all co-authors for their outstanding work and collaboration! The article can be accessed here: https://pubs.acs.org/doi/full/10.1021/acsptsci.5c00767

Recent Publication: How Tiny Molecules Shape the Flexibility of Cell Membranes

By Sunghee Lee • November 15, 2025
Our research team has uncovered new details about how small oil-like molecules influence the thickness and flexibility of cell membranes. These membranes, built from layers of lipids, contain tiny pockets of free space that help control how soft, dense, or permeable the membrane is. Our research team found that some smaller molecules can fit into these layers, making the membrane thicker, while larger or crystallizing ones get pushed out, leading to thinning. These changes help explain how different molecules inside a membrane affect its overall structure and function. This study not only expands our understanding of how biological membranes work but also points to new possibilities for creating custom-designed synthetic membranes for research and technology. Read more details here: https://pubs.acs.org/doi/10.1021/acs.jpcb.5c06296 Congratulations to the Project Symphpony team for their exciting findings and continued dedication to advancing membrane science!
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