A dual-constriction biological nanopore resolves homonucleotide sequences with high fidelity.

Abstract

Single-molecule long-read DNA sequencing with biological nanopores is fast and high-throughput but suffers reduced accuracy in homonucleotide stretches. We now combine the CsgG nanopore with the 35-residue N-terminal region of its extracellular interaction partner CsgF to produce a dual-constriction pore with improved signal and basecalling accuracy for homopolymer regions. The electron cryo-microscopy structure of CsgG in complex with full-length CsgF shows that the 33 N-terminal residues of CsgF bind inside the β-barrel of the pore, forming a defined second constriction. In complexes of CsgG bound to a 35-residue CsgF constriction peptide, the second constriction is separated from the primary constriction by ~25 Å. We find that both constrictions contribute to electrical signal modulation upon ssDNA translocation. DNA sequencing using a prototype CsgG:CsgF protein pore with two constrictions improved single-read accuracy by 25 to 70 % in homopolymers up to 9 nucleotides long.