Translocation of Precision Polymers through Biological Nanopores

Macromol Rapid Commun. 2017 Dec;38(24). doi: 10.1002/marc.201700680. Epub 2017 Nov 16.

Abstract

Nanopore analysis, which is, currently, chiefly used for DNA sequencing, is also an appealing technique for characterizing abiotic polymers. As a first step toward this goal, nanopore detection of non-natural monodispersed poly(phosphodiester)s as candidate backbone structures is reported herein. Two model homopolymers containing phosphopropyl repeat units (i.e., 56 or 104 r.u.) and a short thymidine nucleotide sequence are analyzed in the present work. They are tested in two different biological nanopores, α-hemolysin from Staphylococcus aureus, and aerolysin from Aeromonas hydrophila. These recordings are performed in aqueous medium at different KCl concentrations and various driving voltages. The data show a complex interaction with evidence for voltage dependence and threading, and underline the influence of the molecular structure and orientation of the precision poly(phosphodiester)s on the observed residual current signal as well as on the translocation dynamics. In particular, they suggest a dominant entropic contribution due to the high flexibility of the phosphodiester homopolymer.

Keywords: aerolysin; hemolysin; nanopore sequencing; polymer characterization; precision polymers.

MeSH terms

  • Aeromonas hydrophila / chemistry*
  • Bacterial Toxins / analysis*
  • Entropy
  • Hemolysin Proteins / analysis*
  • Nanopores
  • Organophosphates / chemistry*
  • Polymers / chemistry*
  • Pore Forming Cytotoxic Proteins / analysis*
  • Staphylococcus aureus / chemistry*

Substances

  • Bacterial Toxins
  • Hemolysin Proteins
  • Organophosphates
  • Polymers
  • Pore Forming Cytotoxic Proteins
  • aerolysin