Experimentally Probing the Effect of Confinement Geometry on Lipid Diffusion

被引:1
|
作者
Voce, Nicole [1 ]
Stevenson, Paul [1 ]
机构
[1] Northeastern Univ, Dept Phys, Boston, MA 02115 USA
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 2024年 / 128卷 / 18期
关键词
FLUORESCENCE CORRELATION SPECTROSCOPY; SUPPORTED PHOSPHOLIPID-BILAYERS; LATERAL DIFFUSION; PLASMA-MEMBRANE; PHOSPHATIDYL SERINE; NARROW ESCAPE; RECOVERY; VOLUME; FLUID; PROTEIN;
D O I
10.1021/acs.jpcb.3c07388
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The lateral mobility of molecules within the cell membrane is ultimately governed by the local environment of the membrane. Confined regions induced by membrane structures, such as protein aggregates or the actin meshwork, occur over a wide range of length scales and can impede or steer the diffusion of membrane components. However, a detailed picture of the origins and nature of these confinement effects remains elusive. Here, we prepare model lipid systems on substrates patterned with confined domains of varying geometries constructed with different materials to explore the influences of physical boundary conditions and specific molecular interactions on diffusion. We demonstrate a platform that is capable of significantly altering and steering the long-range diffusion of lipids by using simple oxide deposition approaches, enabling us to systematically explore how confinement size and shape impact diffusion over multiple length scales. While we find that a "boundary condition" description of the system captures underlying trends in some cases, we are also able to directly compare our systems to analytical models, revealing the unexpected breakdown of several approximate solutions. Our results highlight the importance of considering the length scale dependence when discussing properties such as diffusion.
引用
收藏
页码:4404 / 4413
页数:10
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