Journal
NUCLEIC ACIDS RESEARCH
Volume 45, Issue 21, Pages 12057-12068Publisher
OXFORD UNIV PRESS
DOI: 10.1093/nar/gkx990
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Funding
- New York University Abu Dhabi Research Enhancement Fund award [RE082]
- Al Jalila Foundation Research Center seed grant [AJF201624]
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We have developed a novel approach for creating membrane-spanning protein-based pores. The construction principle is based on using well-defined, circular DNA nanostructures to arrange a precise number of pore-forming protein toxin monomers. We can thereby obtain, for the first time, protein pores with specifically set diameters. We demonstrate this principle by constructing artificial alpha-hemolysin (alpha HL) pores. The DNA/alpha HL hybrid nanopores composed of twelve, twenty or twenty-six monomers show stable insertions into lipid bilayers during electrical recordings, along with steady, pore size-dependent current levels. Our approach successfully advances the applicability of nanopores, in particular towards label-free studies of single molecules in large nanoscaled biological structures.
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