bioRxiv · 10.1101/2024.11.27.625717
Mechanistic Insight into pH-Driven Phase Transition of Lipid Nanoparticles
Abstract
The functionality of lipid nanoparticles (LNPs) as delivery systems in mRNA-based therapeutics is intricately linked to the protonation behavior of their aminolipid components. This study employs large-scale constant-pH molecular dynamics (CpHMD) simulations to decode the environment-dependent pKa of aminolipids in the Comirnaty lipid formulation, providing a detailed view of their pH-dependent structural dynamics. Our results reveal a significant shift in the apparent pKa of the aminolipid ALC-0315, from an intrinsic value of 9.3 in water to 4.9 within the LNP environment. This shift arises from the interplay between lipid reorganization and local electrostatic interactions, resulting in distinct protonation states across the LNP core and surface. At low pH, protonated aminolipids dominate the LNP surface, promoting efficient mRNA encapsulation, whereas at neutral pH, deprotonated aminolipids migrate to the hydrophobic core, driving structural stabilization. Notably, the localized pKa of aminolipids varies significantly with their position, decreasing from near-surface regions (7 to 8) to the hydrophobic core ([≤]4). These findings elucidate the molecular mechanisms underpinning LNP phase transitions and highlight the key role of pKa shifts for the design of aminolipids and for optimizing LNP compositions for enhanced therapeutic delivery. This study bridges experimental observations with molecular-level insights, advancing the rational development of next-generation lipid-based nanocarriers.
Source connections
Explore related subjects
Keep this discovery
Explore connections, maps & timelines
Trollmann, M. F., Böckmann, R. A.. 2024-11-29. Mechanistic Insight into pH-Driven Phase Transition of Lipid Nanoparticles. https://doi.org/10.1101/2024.11.27.625717
Cite the original work for its findings. Save a collection to share your selection of sources.