Discrimination of single base substitutions in a DNA strand immobilized in a biological nanopore.

Nanopores have been explored as highly sensitive sensors for detection and rapid sequencing of single molecules of DNA. To sequence DNA with a nanopore requires that adenine (A), cytosine (C), thymine (T), and guanine (G) produce distinct current signals as they traverse the pore. Recently, we demonstrated that homopolymers of adenine, cytosine, and thymine immobilized in the nanopore protein alpha-hemolysin (alphaHL) produced distinct current blockades dependent on their chemical orientation.

Nucleotide identification and orientation discrimination of DNA homopolymers immobilized in a protein nanopore.

Nanopores have been used as extremely sensitive resistive pulse sensors to detect analytes at the molecular level. There has been interest in using such a scheme to rapidly and inexpensively sequence single molecules of DNA. To establish reference current levels for adenine, cytosine, and thymine nucleotides, we measured the blockage currents following immobilization of single-stranded DNA polyadenine, polycytosine, and polythymine within a protein nanopore in chemical orientations in which either the 3' or the 5' end enters the pore.

Automated formation of lipid-bilayer membranes in a microfluidic device.

Although membrane channel proteins are important to drug discovery and hold great promise as engineered nanopore sensing elements, their widespread application to these areas has been limited by difficulties in fabricating planar lipid-bilayer membranes. We present a method for forming these sub-5-nm-thick free-standing structures based on a self-assembly process driven by solvent extraction in a microfluidic channel. This facile automatable process forms high-quality membranes able to host channel proteins measurable at single-molecule conductance resolution.