Conical nanopore membranes: Controlling the nanopore shape

Conical nanopore membranes: Controlling the nanopore shape
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DOI:
10.1002/smll.200500196
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发表时间:
2006-02-01
期刊:
影响因子:
13.3
通讯作者:
Martin, CR
Martin, CR
中科院分区:
材料科学1区
文献类型:
--
作者:
Harrell, CC;Siwy, ZS;Martin, CR

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There is increasing interest in using nanopores as the sensing elements in biosensors.[1–6] The α-hemolysin protein nanopore is typically used, and this sensor consists of a single protein nanopore embedded within a lipid bilayer membrane.[1–3] An ionic current is passed through the nanopore, and analyte species are detected as transient blocks in this current associated with translocation of the analyte through the pore; this is known as stochastic or resistivepulse sensing.[1–3] While this is a very promising sensing paradigm, it would be advantageous to eliminate the fragile lipid bilayer membrane and perhaps to replace the biological nanopore with an abiotic equivalent.[7–16] A variety of approaches have been used to prepare abiotic nanopores for resistive-pulse sensing, including focused-ion-beam etching,[7, 8, 11] soft lithography,[10] film embedding of carbon nanotubes,[4] and the track-etch method.[5, 6, 13–17] Conically shaped nanopores [13–17] are especially advantageous for sensing applications.[6, 18] This is because Lee et al. have shown that when an ion current is passed through a conical nanopore, the majority of the resulting transmembrane voltage drop is focused to the electrolyte solution in and near the small-diameter opening (tip opening) of the nanopore.[5] As a result, there is a “sensing zone” for analyte species in and near the tip opening.[5, 6] If a means for controlling the cone angle of the conical nanopore were available, the length of this sensing zone, and the field strength within the zone, could be systematically varied. This would allow for tailoring of the nanopore to suit any desired sensing application.We have recently discovered that the cone angle of conical nanopores prepared by anisotropic etching [5, 6, 13–17] of heavy-ion-tracked [19] polymer films can be systematically varied by varying the transmembrane potential difference applied during pore etching. This ability to vary the cone angle was proven by electron microscopy and through electrochemical investigations of the ion current flowing through the nanopore after etching. The results of these investigations are described here.