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

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作者
Benjamin Cressiot
Sandra J. Greive
Mehrnaz Mojtabavi
Alfred A. Antson
Meni Wanunu
机构
[1] Northeastern University,Department of Physics
[2] Northeastern University,Department of Chemistry and Chemical Biology
[3] University of York,York Structural Biology Laboratory, Department of Chemistry
[4] Northeastern University,Department of Bioengineering
[5] Université Paris-Saclay,LAMBE, Université d’Evry Val d’Essonne, Université de Cergy Pontoise, CNRS, CEA
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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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