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9VP3

CryoEM structure of cyclised H-pilus (D69N)

Summary for 9VP3
Entry DOI10.2210/pdb9vp3/pdb
EMDB information65235
DescriptorPilin, 1,2-DIPALMITOYL-PHOSPHATIDYL-GLYCEROLE (2 entities in total)
Functional Keywordspilus, conjugation, filament, protein fibril
Biological sourceSalmonella enterica subsp. enterica serovar Typhi
Total number of polymer chains1
Total formula weight8323.93
Authors
Ishimoto, N.,Beis, K. (deposition date: 2025-07-02, release date: 2025-12-24, Last modification date: 2026-03-18)
Primary citationHe, S.,Ishimoto, N.,Wong, J.L.C.,David, S.,Sanchez-Garrido, J.,Bogdanov, M.,Beis, K.,Frankel, G.
H pilin cyclisation and pilus biogenesis are promiscuous but electrostatic perturbations impair conjugation efficiency.
Nat Commun, 2026
Cited by
PubMed Abstract: During conjugation, plasmid DNA is transferred from donor to recipient bacteria via the plasmid-encoded mating pilus, formed as thin helical assemblies of polymerised pilin subunits. In the IncHI1 R27 plasmid-encoded pilus, the TrhA pilin undergoes cyclisation (via a peptide bond between Gly1 and Asp69), essential for conjugation. Gly1 and Asp69 are exposed on the pilus surface and conserved in all TrhA pilins in the Plascad database. Substituting Asp69 with Asn, Ala, Gly, or Arg does not prevent cyclisation or pilus formation, which remains structurally indistinguishable from the wild type. Conjugation efficiency of the Asp69 substitutions across multiple recipient species correlates with side chain size, in the order Asp69Asn > Asp69Ala > Asp69Gly. However, Asp69Arg, as well as Asp69Lys and Gly1Lys substitutions abolish conjugation, likely due to the positively charged pilus surface (opposite to the wild-type negative charge) forming unfavourable electrostatic interactions with the recipient outer membrane's inner leaflet, composed solely of zwitterionic phosphatidylethanolamine (PE). Consistently, conjugation is rescued in recipients lacking PE. These findings indicate strong selective pressure to maintain Gly1 and Asp69, as efficient DNA transfer depends on precise electrostatic and steric constraints of the pilus surface.
PubMed: 41708604
DOI: 10.1038/s41467-026-69599-3
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (2.88 Å)
Structure validation

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