Off-target structural insights: ArnA and AcrB in bacterial membrane-protein cryo-EM analysis

Acta Crystallogr D Struct Biol. 2025 Oct 1;81(Pt 10):545-557. doi: 10.1107/S2059798325007089. Epub 2025 Sep 10.

Abstract

Membrane-protein quality control in Escherichia coli involves coordinated actions of the AAA+ protease FtsH, the insertase YidC and the regulatory complex HflKC. These systems maintain proteostasis by facilitating membrane-protein insertion, folding and degradation. To gain structural insights into a putative complex formed by FtsH and YidC, we performed single-particle cryogenic electron microscopy on detergent-solubilized membrane samples, from which FtsH and YidC were purified using Ni-NTA affinity and size-exclusion chromatography. Although SDS-PAGE analysis indicated high purity of these proteins, cryo-EM data sets unexpectedly yielded high-resolution structures of ArnA and AcrB at 4.0 and 2.9 Å resolution, respectively. ArnA is a bifunctional enzyme involved in lipid A modification and polymyxin resistance, while AcrB is a multidrug efflux transporter of the AcrAB-TolC system. ArnA and AcrB, known Ni-NTA purification contaminants, were also consistently detected by mass spectrometry in Strep-Tactin affinity-purified samples, validating their presence independently of affinity-tag selection. ArnA, which is typically cytoplasmic, was consistently found in membrane-isolated samples, indicating an association with membrane components. Only 2D class averages corresponding to the cytoplasmic AAA+ domain of FtsH were observed; neither side views of full-length FtsH nor densities corresponding to an intact FtsH-YidC complex could be identified, due to the conformational flexibility of the FtsH complex and its transient interaction with YidC, which limited particle alignment and stable classification in cryo-EM data sets. Two-dimensional class averages revealed additional particles resembling GroEL and cytochrome bo3 oxidase. These results underscore the utility of cryo-EM in uncovering off-target yet structurally well defined complexes, which may reflect physiologically relevant interactions or purification biases during membrane-protein overexpression.

Keywords: AcrB; ArnA; cryo-EM; membrane-protein expression; protein quality control.

MeSH terms

  • Cryoelectron Microscopy / methods
  • Escherichia coli Proteins* / chemistry
  • Escherichia coli Proteins* / metabolism
  • Escherichia coli Proteins* / ultrastructure
  • Escherichia coli* / chemistry
  • Escherichia coli* / metabolism
  • Membrane Proteins* / chemistry
  • Membrane Transport Proteins* / chemistry
  • Models, Molecular
  • Multidrug Resistance-Associated Proteins* / chemistry
  • Multidrug Resistance-Associated Proteins* / metabolism
  • Protein Conformation

Substances

  • Escherichia coli Proteins
  • AcrB protein, E coli
  • Multidrug Resistance-Associated Proteins
  • Membrane Transport Proteins
  • Membrane Proteins
  • YIDC protein, E coli