Nanoscale patterning controls inorganic-membrane interface structure

被引:15
作者
Almquist, Benjamin D. [1 ]
Verma, Piyush [1 ]
Cai, Wei [2 ]
Melosh, Nicholas A. [1 ]
机构
[1] Stanford Univ, Dept Mat Sci & Engn, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Mech Engn, Stanford, CA 94305 USA
基金
美国国家科学基金会;
关键词
MOLECULAR-DYNAMICS SIMULATIONS; LIPID-BILAYERS; COMPUTER-SIMULATIONS; SILICON NANOWIRES; CHANNEL FUNCTION; TRANSIENT PORES; GIANT VESICLES; LINE TENSION; FUSION; MECHANISM;
D O I
10.1039/c0nr00486c
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
The ability to non-destructively integrate inorganic structures into or through biological membranes is essential to realizing full bio-inorganic integration, including arrayed on-chip patch-clamps, drug delivery, and biosensors. Here we explore the role of nanoscale patterning on the strength of biomembrane-inorganic interfaces. AFM measurements show that inorganic probes functionalized with hydrophobic bands with thicknesses complimentary to the hydrophobic lipid bilayer core exhibit strong attachment in the bilayer. As hydrophobic band thickness increases to 2-3 times the bilayer core the interfacial strength decreases, comparable to homogeneously hydrophobic probes. Analytical calculations and molecular dynamics simulations predict a transition between a 'fused' interface and a 'T-junction' that matches the experimental results, showing lipid disorder and defect formation for thicker bands. These results show that matching biological length scales leads to more intimate bio-inorganic junctions, enabling rational design of non-destructive membrane interfaces.
引用
收藏
页码:391 / 400
页数:10
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