Completed Cells, Biochemistry & Physiology Genetics & Molecular Biology

Actin-like cytoskeletal systems in bacteria and archaea

In plain English

AI plain-English summary

Inside many bacteria and archaea, tiny protein filaments—cousins of the actin that shapes human cells—are pulling, pushing, and organising the microbial interior. This project aims to work out exactly how these filaments, and the helper proteins that control them, perform their jobs. The problem is that we know these filaments exist and that they matter for basic microbial life, but the molecular details of how they work remain murky. For example, the MreB filament helps rod-shaped bacteria keep their form; MamK lines up magnetic crystals inside magnetotactic bacteria; and ParM builds a spindle to split DNA copies during cell division. Without understanding the mechanics, we cannot grasp how these organisms function or evolve. This is fundamental science—there is no immediate medical or industrial application. But the work could eventually reveal how simple protein scaffolds evolved into the sophisticated cytoskeletons that underpin all complex life. Past discoveries about bacterial filaments have already led to new antibiotics that target cell shape. Deeper knowledge here might one day help engineer bacteria for tasks such as targeted drug delivery or biomineral production, or simply rewrite the textbook on how cells organise themselves.

View original technical description
Many bacteria and archaea contain cytomotive filaments consisting of proteins that are related in subunit and protofilament structure to eukaryotic actin. Our goal is to understand the molecular mechanisms that these filaments and their accessory factors employ in order to facilitate a diverse set of cell biological phenomena. We propose to discover how MreB maintains cell shape in non-round cells and, in particular, what is the role of filaments in this system. We will investigate MamK and how it aligns magnetosomes along its filaments. ParM filaments form antiparallel spindles during plasmid segregation and we propose to unravel the ParRC-accelerated formin-like polymerisation mechanism at the filament tips. Also, we plan to work on not so well-characterised systems such as crenactin and other Alps for which basic functions need to be discovered. Finally, we will work on technology developments for electron cryotomography, producing clonable, monovalent ferritin-based electron dense labels and performing FIB milling procedures that yield isotropic maps of entire cells containing filaments at molecular resolution. Overall, we will discover and describe how cytomotive filament systems with actin at their centre, presumably having originated from a simple common ancestor, developed into sophisticated machinery that operates on otherwise inaccessible length scales.

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Researchers

Jan Löwe (EPMC Awardee)

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Original classification

Investigator Award in Science

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