| Literature DB >> 33349702 |
Conor Lanphere1, Daniel Offenbartl-Stiegert1, Adam Dorey1, Genevieve Pugh1, Elena Georgiou1, Yongzheng Xing1, Jonathan R Burns2, Stefan Howorka3.
Abstract
DNA nanopores are bio-inspired nanostructures that control molecular transport across lipid bilayer membranes. Researchers can readily engineer the structure and function of DNA nanopores to synergistically combine the strengths of DNA nanotechnology and nanopores. The pores can be harnessed in a wide range of areas, including biosensing, single-molecule chemistry, and single-molecule biophysics, as well as in cell biology and synthetic biology. Here, we provide a protocol for the rational design of nanobarrel-like DNA pores and larger DNA origami nanopores for targeted applications. We discuss strategies for the pores' chemical modification with lipid anchors to enable them to be inserted into membranes such as small unilamellar vesicles (SUVs) and planar lipid bilayers. The procedure covers the self-assembly of DNA nanopores via thermal annealing, their characterization using gel electrophoresis, purification, and direct visualization with transmission electron microscopy and atomic force microscopy. We also describe a gel assay to determine pore-membrane binding and discuss how to use single-channel current recordings and dye flux assays to confirm transport through the pores. We expect this protocol to take approximately 1 week to complete for DNA nanobarrel pores and 2-3 weeks for DNA origami pores.Entities:
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Year: 2020 PMID: 33349702 DOI: 10.1038/s41596-020-0331-7
Source DB: PubMed Journal: Nat Protoc ISSN: 1750-2799 Impact factor: 13.491