Profiling the chemistry- and confinement-controlled sensing capability of an octameric aerolysin-like protein

Chem Commun (Camb). 2023 May 11;59(39):5850-5853. doi: 10.1039/d3cc01114c.

Abstract

Octameric Aep1 was employed, for the first time to the best of our knowledge, as a nanopore to expand applications. After investigating the optimized conditions of Aep1 for single-channel recording, the sensing features were characterized. Cyclic and linear molecules of varying sizes and charges were employed to probe the radius and chemical environment of the pore, providing deep insights for expected future endeavors at predicting the structure of octameric Aep1. γ-CD showed unique suitability as an 8-subunit adapter in octameric Aep1, enabling the discrimination of β-nicotinamide mononucleotide.

MeSH terms

  • Bacterial Toxins* / chemistry
  • Nanopores*
  • Pore Forming Cytotoxic Proteins / chemistry
  • Proteins

Substances

  • aerolysin
  • Proteins
  • Bacterial Toxins
  • Pore Forming Cytotoxic Proteins