TY - JOUR
T1 - A large size-selective DNA nanopore with sensing applications
AU - Thomsen, Rasmus Peter
AU - Malle, Mette Galsgaard
AU - Okholm, Anders Hauge
AU - Krishnan, Swati
AU - Nielsen, Søren Schmidt-Rasmussen
AU - Sørensen, Rasmus Schøler
AU - Ries, Oliver
AU - Vogel, Stefan
AU - Simmel, Friedrich
AU - Hatzakis, Nikos
AU - Kjems, Jørgen
PY - 2019/12/11
Y1 - 2019/12/11
N2 - Transmembrane nanostructures like ion channels and transporters perform key biological functions by controlling flow of molecules across lipid bilayers. Much work has gone into engineering artificial nanopores and applications in selective gating of molecules, label-free detection/sensing of biomolecules and DNA sequencing have shown promise. Here, we use DNA origami to create a synthetic 9 nm wide DNA nanopore, controlled by programmable, lipidated flaps and equipped with a size-selective gating system for the translocation of macromolecules. Successful assembly and insertion of the nanopore into lipid bilayers are validated by transmission electron microscopy (TEM), while selective translocation of cargo and the pore mechanosensitivity are studied using optical methods, including single-molecule, total internal reflection fluorescence (TIRF) microscopy. Size-specific cargo translocation and oligonucleotide-triggered opening of the pore are demonstrated showing that the DNA nanopore can function as a real-time detection system for external signals, offering potential for a variety of highly parallelized sensing applications.
AB - Transmembrane nanostructures like ion channels and transporters perform key biological functions by controlling flow of molecules across lipid bilayers. Much work has gone into engineering artificial nanopores and applications in selective gating of molecules, label-free detection/sensing of biomolecules and DNA sequencing have shown promise. Here, we use DNA origami to create a synthetic 9 nm wide DNA nanopore, controlled by programmable, lipidated flaps and equipped with a size-selective gating system for the translocation of macromolecules. Successful assembly and insertion of the nanopore into lipid bilayers are validated by transmission electron microscopy (TEM), while selective translocation of cargo and the pore mechanosensitivity are studied using optical methods, including single-molecule, total internal reflection fluorescence (TIRF) microscopy. Size-specific cargo translocation and oligonucleotide-triggered opening of the pore are demonstrated showing that the DNA nanopore can function as a real-time detection system for external signals, offering potential for a variety of highly parallelized sensing applications.
KW - Nanopore, DNA, microscopy
U2 - 10.1038/s41467-019-13284-1
DO - 10.1038/s41467-019-13284-1
M3 - Journal article
C2 - 31827087
VL - 10
JO - Nature Communications
JF - Nature Communications
SN - 2041-1723
M1 - 5655
ER -