Structure of the calcium-dependent type 2 secretion pseudopilus.

Abstract

Many Gram-negative bacteria use type 2 secretion systems (T2SS) to secrete proteins involved in virulence and adaptation. Transport of folded proteins via T2SS nanomachines requires the assembly of inner membrane-anchored fibers called pseudopili. Although efficient pseudopilus assembly is essential for protein secretion, structure-based functional analyses are required to unravel the mechanistic link between these processes. Here, we report an atomic model for a T2SS pseudopilus from Klebsiella oxytoca, obtained by fitting the NMR structure of its calcium-bound subunit PulG into the ~ 5 Å resolution cryo-electron microscopy (cryoEM) reconstruction of assembled fibers. This structure reveals the comprehensive network of inter-subunit contacts and unexpected features, including a disordered central region of the PulG helical stem, and highly flexible C-terminal residues on the fiber surface. NMR, mutagenesis and functional analyses highlight the key role of calcium in PulG folding and stability. Fiber disassembly in the absence of calcium provides a basis for pseudopilus length control, essential for protein secretion, and supports the Archimedes' screw model for T2S mechanism.