Stochastic Sensing of TNT with a Genetically Engineered Pore

Abstract Engineered versions of the transmembrane protein pore α‐hemolysin (αHL) can be used as stochastic sensing elements for the identification and quantification of a wide variety of analytes at the single‐molecule level. Until now, nitroaromatic analytes have eluded detection by this approach. We now report that binding sites for nitroaromatics can be built within the lumen of the αHL pore from simple rings of seven aromatic amino acid side chains (Phe, Tyr or Trp). By monitoring the ionic current that passes through a single pore at a fixed applied potential, various nitroaromatics can be distinguished from TNT on the basis of the amplitude and duration of individual current‐blocking events. Rings of less than seven aromatics bind the analytes more weakly; this suggests that direct aromatic–aromatic interactions are involved. The engineered pores should be useful for the detection of explosives and, in combination with computational approaches and structural analysis, they could further our understanding of noncovalent interactions between aromatic molecules.