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ACS Nano. 2011 Dec 27;5(12):9345-53. doi: 10.1021/nn203764j. Epub 2011 Nov 16.

Nanopore analysis of individual RNA/antibiotic complexes.

Author information

1
Department of Physics, Northeastern University, Boston, Massachusetts 02115, United States. wanunu@neu.edu

Abstract

Nanopores in thin solid-state membranes are used to rapidly analyze individual RNA/drug complexes. The interactions of a truncated A-site RNA model of the prokaryotic ribosome with aminoglycoside antibiotics are characterized by passing individual molecules through a 3-3.5 nm diameter pore fabricated in a 8-10 nm thick silicon nitride membrane. Complexes of the A-site RNA with aminoglycosides can be distinguished from unbound A-site based on the ion current signatures produced as they pass through the nanopores. Counting the fraction of free and drug-bound molecules affords label-free drug-RNA binding isotherms consistent with literature reports and with data generated using independent fluorescence-based assays. Our measurements are supported by molecular dynamics simulations, which illustrate the relationship between the ionic current and complexation of the A-site RNA with paramomycin, a prototypical aminoglycoside antibiotic.

PMID:
22067050
PMCID:
PMC3253136
DOI:
10.1021/nn203764j
[Indexed for MEDLINE]
Free PMC Article

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