Thermostable virus portal proteins as reprogrammable adapters for solid-state nanopore sensors

被引:41
作者
Cressiot, Benjamin [1 ,2 ,5 ]
Greive, Sandra J. [3 ]
Mojtabavi, Mehrnaz [4 ]
Antson, Alfred A. [3 ]
Wanunu, Meni [1 ,2 ]
机构
[1] Northeastern Univ, Dept Phys, Boston, MA 02115 USA
[2] Northeastern Univ, Dept Chem & Chem Biol, Boston, MA 02115 USA
[3] Univ York, Dept Chem, York Struct Biol Lab, York YO10 5DD, N Yorkshire, England
[4] Northeastern Univ, Dept Bioengn, Boston, MA 02115 USA
[5] Univ Paris Saclay, Univ Evry Val Essonne, Univ Cergy Pontoise, LAMBE,CNRS,CEA, F-91025 Evry, France
基金
英国生物技术与生命科学研究理事会;
关键词
ALPHA-HEMOLYSIN NANOPORE; DNA TRANSPORT; RNA MOLECULES; SINGLE; TRANSLOCATION; PORE; PEPTIDES; ACID; DISCRIMINATION; DYNAMICS;
D O I
10.1038/s41467-018-07116-x
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Nanopore-based sensors are advancing the sensitivity and selectivity of single-molecule detection in molecular medicine and biotechnology. Current electrical sensing devices are based on either membrane protein pores supported in planar lipid bilayers or solid-state (SS) pores fabricated in thin metallic membranes. While both types of nanosensors have been used in a variety of applications, each has inherent disadvantages that limit its use. Hybrid nanopores, consisting of a protein pore supported within a SS membrane, combine the robust nature of SS membranes with the precise and simple engineering of protein nanopores. We demonstrate here a novel lipid-free hybrid nanopore comprising a natural DNA pore from a thermostable virus, electrokinetically inserted into a larger nanopore supported in a silicon nitride membrane. The hybrid pore is stable and easy to fabricate, and, most importantly, exhibits low peripheral leakage allowing sensing and discrimination among different types of biomolecules.
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页数:7
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