posted on 2025-08-27, 19:10authored bySian Kang Chong, Xinwen Miao, Samuel J. W. Chan, Ji-Yu Zhu, Simou Sun, Yihang Liu, Xiangfu Guo, Zihui Fan, Yi Teng Lau, James C. S. Ho, Atul N. Parikh, Guillermo C. Bazan, Wenting Zhao
Conjugated oligoelectrolytes (COEs) constitute a powerful
toolbox for
detecting and modulating cell membrane properties. The versatility
in their molecular structural design enables fine-tuning of their
membrane intercalating behaviors, ranging from membrane disruption
for antimicrobial applications to membrane stabilization for cell
labeling and biosensing. However, a detailed description of the intercalation
mechanism is absent, despite efforts to understand the impact of charge
density and hydrophobic core length on the membrane intercalation
efficiency of COEs. A critical yet overlooked factor is membrane curvature,
which has been shown to modulate the spatiotemporal organization of
molecules on cell membranes. Here, we found that nanoscale curved
membranes serve as “hotspots” for COE intercalation.
Using designed nanobar arrays with a gradient geometry, we generated
nanobar-supported lipid bilayers with predefined membrane curvatures.
Curvature-correlated spatial enrichment of COEs was observed on nanobars
with curved ends of 600 nm diameter or below in a time-dependent manner.
Higher membrane curvature corresponded to a faster COE intercalation
rate and higher equilibrium capacity. Comparing COEs with different
chemical structures, those with shorter hydrophobic cores and lower
charge densities promoted more curvature-guided membrane intercalation.
Membranes with increased surface charges or more lipid packing defects
further reinforced the curvature preference of the COEs. These results
indicate that membrane curvature plays a significant role in the spatiotemporal
modulation of COE-membrane intercalation, forming strategies for tailored
molecular designs to target cellular membranes of different shapes.