Active Cells, Biochemistry & Physiology Genetics & Molecular Biology

Towards a molecular understanding of bacterial Type IV filament systems

In plain English

AI plain-English summary

Bacteria use tiny, retractable grappling hooks—called type IV filaments—to crawl, attack, and infect cells, but no one knows exactly how these nanomachines assemble and move. This project aims to solve that mystery. The molecular motors that build and retract these filaments are found in most bacteria and archaea, yet the fundamental mechanics of how they work remain unknown. Without this knowledge, we cannot block the filaments that many pathogens use to cause disease. The researchers will combine structural biology, light microscopy, and single-molecule imaging to compare two ancient filament systems, revealing principles that predate the split between bacteria and archaea. If successful, the work will produce a molecular blueprint for how these machines couple energy to motion. This is fundamental science—there is no immediate medical application. But a complete understanding of filament assembly could eventually guide the design of anti-virulence drugs that disarm bacteria without killing them, reducing selective pressure for resistance. It could also enable synthetic biologists to build artificial motile systems from the bottom up, mimicking bacterial twitching motility in engineered cells.

View original technical description
Type IV filament systems (T4FS) are multi-component nanomachines spanning the cell envelope of most bacteria and archaea. They have diverse function including motility, bacterial predation and virulence, all of which rely on a shared mechanism involving T4FS-derived pilus filaments. While the principles governing pilus assembly are likely conserved across most T4FS, they remain poorly understood. This proposal addresses this knowledge gap by investigating two archetypal T4FS: the Type IV pilus system (T4PS) and Tad pilus system (TadPS). Key aims include understanding how these systems assemble, how their ultrastructure facilitates pilus extension/retraction, and how the ATPase motors couple nucleotide hydrolysis to the physical processing of pilins. To achieve these aims a multidisciplinary approach is undertaken combining in- vitro and in-cell structural biology, light microscopy, and advanced single- molecule imaging. By comparing the T4PS and TadPS, we uncover fundamental T4FS mechanistic principles that predate the evolutionary divergence of archaea and bacteria. Knowledge learnt will direct bottom-up reconstitution strategies aiming to recreate twitching motility and ultimately directed motion in synthetic cellular systems. This ambitious program seeks a molecular understanding of the TadPS and T4PS. It describes how these systems promote bacterial pathogenesis and facilitates development of targeted anti-virulence therapeutics.

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Researchers

Harry Low (EPMC Awardee)

Related Research

Grants with similar aims, by meaning.

Unraveling type IV pilus assembly
The bacterial type IV pilus machinery as a DNA translocator
Investigating structure, dynamics and mechanism of the bacterial type IV pilus machinery
Functional analysis of the proteins and multiprotein complexes involved in the biogenesis of type IV pili
Actin-like cytoskeletal systems in bacteria and archaea

Original classification

Discovery Award

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