Voltage-Controlled Metal Binding on Polyelectrolyte-Functionalized Nanopores

被引:52
作者
Actis, Paolo [1 ,2 ,3 ,4 ]
Vilozny, Boaz [1 ,3 ,4 ]
Seger, R. Adam [1 ,3 ,4 ]
Li, Xiang [1 ]
Jejelowo, Olufisayo [2 ]
Rinaudo, Marguerite [5 ]
Pourmand, Nader [1 ,2 ]
机构
[1] Univ Calif Santa Cruz, Dept Biomol Engn, Santa Cruz, CA 95064 USA
[2] Texas So Univ, Dept Biol, Houston, TX 77004 USA
[3] UC Santa Cruz, Adv Studies Labs, Moffett Field, CA 94035 USA
[4] NASA, Ames Res Ctr, Moffett Field, CA 94035 USA
[5] Univ Grenoble 1, CNRS, Ctr Rech Macromol Vegetales CERMAV, CNRS, F-38041 Grenoble 9, France
基金
美国国家卫生研究院; 美国国家航空航天局;
关键词
CURRENT RECTIFICATION; CHITOSAN; COPPER; DNA;
D O I
10.1021/la2005612
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Most of the research in the field of nanopore-based platforms is focused on monitoring ion currents and forces as individual molecules translocate through the nanopore. Molecular gating, however, can occur when target analytes interact with receptors appended to the nanopore surface. Here we show that a solid state nanopore functionalized with polyelectrolytes can reversibly bind metal ions, resulting in a reversible, real-time signal that is concentration dependent. Functionalization of the sensor is based on electrostatic interactions, requires no covalent bond formation, and can be monitored in real time. Furthermore, we demonstrate how the applied voltage can be employed to tune the binding properties of the sensor. The sensor has wide-ranging applications and, its simplest incarnation can be used to study binding thermodynamics using purely electrical measurements with no need for labeling.
引用
收藏
页码:6528 / 6533
页数:6
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