<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Cao C</dc:creator>
  <dc:creator>Li MY</dc:creator>
  <dc:creator>Cirauqui N</dc:creator>
  <dc:creator>Wang YQ</dc:creator>
  <dc:creator>Dal Peraro M</dc:creator>
  <dc:creator>Tian H</dc:creator>
  <dc:creator>Long YT</dc:creator>
  <dc:date>2018</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Nanopore sensing is a powerful single-molecule method for DNA and protein sequencing. Recent studies have demonstrated that aerolysin exhibits a high sensitivity for single-molecule detection. However, the lack of the atomic resolution structure of aerolysin pore has hindered the understanding of its sensing capabilities. Herein, we integrate nanopore experimental results and molecular simulations based on a recent pore structural model to precisely map the sensing spots of this toxin for ssDNA translocation. Rationally probing ssDNA length and composition upon pore translocation provides new important insights for molecular determinants of the aerolysin nanopore. Computational and experimental results reveal two critical sensing spots (R220, K238) generating two constriction points along the pore lumen. Taking advantage of the sensing spots, all four nucleobases, cytosine methylation and oxidation of guanine can be clearly identified in a mixture sample. The results provide evidence for the potential of aerolysin as a nanosensor for DNA sequencing.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://sonar.ch/global/documents/10399</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1038/s41467-018-05108-5</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/pmid/30026547</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:source>Nature communications. - 2018</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Bacterial Toxins</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Binding Sites</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">DNA, Single-Stranded</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">Lipid Bilayers</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">Molecular Dynamics Simulation</dc:subject>
  <dc:subject xmlns:ns6="xml" ns6:lang="en">Nanopores</dc:subject>
  <dc:subject xmlns:ns7="xml" ns7:lang="en">Nanotechnology</dc:subject>
  <dc:subject xmlns:ns8="xml" ns8:lang="en">Nucleic Acid Conformation</dc:subject>
  <dc:subject xmlns:ns9="xml" ns9:lang="en">Oligonucleotides</dc:subject>
  <dc:subject xmlns:ns10="xml" ns10:lang="en">Phosphatidylcholines</dc:subject>
  <dc:subject xmlns:ns11="xml" ns11:lang="en">Pore Forming Cytotoxic Proteins</dc:subject>
  <dc:subject xmlns:ns12="xml" ns12:lang="en">Protein Binding</dc:subject>
  <dc:subject xmlns:ns13="xml" ns13:lang="en">Protein Conformation, beta-Strand</dc:subject>
  <dc:subject xmlns:ns14="xml" ns14:lang="en">Protein Interaction Domains and Motifs</dc:subject>
  <dc:subject xmlns:ns15="xml" ns15:lang="en">Sequence Analysis, DNA</dc:subject>
  <dc:title xmlns:ns16="xml" ns16:lang="en">Mapping the sensing spots of aerolysin for single oligonucleotides analysis.</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
