TY - JOUR
T1 - Curvature-Assisted Vesicle Explosion Under Light-Induced Asymmetric Oxidation
AU - Malik, Vinit Kumar
AU - Pak, On Shun
AU - Feng, Jie
N1 - V.K.M. and J.F. acknowledge partial support by the National Science Foundation (NSF) under grant No. CBET 2323045. O.S.P. acknowledges partial support by NSF under grant No. CBET 2323046. We also acknowledge the use of facilities and instumentation at the Materials Research Laboratory Central Research Facilities, University of Illinois, for the confocal experiments. The authors also appreciate the anonymous reviewers for their numerous insightful suggestions in improving this manuscript.
PY - 2024/10/16
Y1 - 2024/10/16
N2 - Exposure of cell membranes to reactive oxygen species can cause oxidation of membrane lipids. Oxidized lipids undergo drastic conformational changes, compromising the mechanical integrity of the membrane and causing cell death. For giant unilamellar vesicles, a classic cell mimetic system, a range of mechanical responses under oxidative assault has been observed including formation of nanopores, transient micron-sized pores, and total sudden catastrophic collapse (i.e., explosion). However, the physical mechanism regarding how lipid oxidation causes vesicles to explode remains elusive. Here, with light-induced asymmetric oxidation experiments, the role of spontaneous curvature on vesicle instability and its link to the conformational changes of oxidized lipid products is systematically investigated. A comprehensive membrane model is proposed for pore-opening dynamics incorporating spontaneous curvature and membrane curling, which captures the experimental observations well. The kinetics of lipid oxidation are further characterized and how light-induced asymmetric oxidation generates spontaneous curvature in a non-monotonic temporal manner is rationalized. Using the framework, a phase diagram with an analytical criterion to predict transient pore formation or catastrophic vesicle collapse is provided. The work can shed light on understanding biomembrane stability under oxidative assault and strategizing release dynamics of vesicle-based drug delivery systems.
AB - Exposure of cell membranes to reactive oxygen species can cause oxidation of membrane lipids. Oxidized lipids undergo drastic conformational changes, compromising the mechanical integrity of the membrane and causing cell death. For giant unilamellar vesicles, a classic cell mimetic system, a range of mechanical responses under oxidative assault has been observed including formation of nanopores, transient micron-sized pores, and total sudden catastrophic collapse (i.e., explosion). However, the physical mechanism regarding how lipid oxidation causes vesicles to explode remains elusive. Here, with light-induced asymmetric oxidation experiments, the role of spontaneous curvature on vesicle instability and its link to the conformational changes of oxidized lipid products is systematically investigated. A comprehensive membrane model is proposed for pore-opening dynamics incorporating spontaneous curvature and membrane curling, which captures the experimental observations well. The kinetics of lipid oxidation are further characterized and how light-induced asymmetric oxidation generates spontaneous curvature in a non-monotonic temporal manner is rationalized. Using the framework, a phase diagram with an analytical criterion to predict transient pore formation or catastrophic vesicle collapse is provided. The work can shed light on understanding biomembrane stability under oxidative assault and strategizing release dynamics of vesicle-based drug delivery systems.
KW - biomedical engineering
KW - light-induced membrane oxidation
KW - lipid vesicles
KW - membrane modeling
KW - spontaneous curvature
UR - http://www.scopus.com/inward/record.url?scp=85200997100&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85200997100&partnerID=8YFLogxK
U2 - 10.1002/advs.202400504
DO - 10.1002/advs.202400504
M3 - Article
C2 - 39136143
AN - SCOPUS:85200997100
SN - 2198-3844
VL - 11
JO - Advanced Science
JF - Advanced Science
IS - 38
M1 - 2400504
ER -