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Updated: Mar 18, 2026

Using Microfluidics and Fluorescence Microscopy to Study the Assembly Dynamics of Single Actin Filaments and Bundles
Published on: May 5, 2022
Structure of the magnetosome-associated actin-like MamK filament at subnanometer resolution
Julien R C Bergeron1, Rachel Hutto1, Ertan Ozyamak2
1Department of Biochemistry, University of Washington, Seattle, Washington.
Abstract:
Magnetotactic bacteria possess cellular compartments called magnetosomes that sense magnetic fields. Alignment of magnetosomes in the bacterial cell is necessary for their function, and this is achieved through anchoring of magnetosomes to filaments composed of the protein MamK. MamK is an actin homolog that polymerizes upon ATP binding. Here, we report the structure of the MamK filament at ∼6.5 Å, obtained by cryo-Electron Microscopy. This structure confirms our previously reported double-stranded, nonstaggered architecture, and reveals the molecular basis for filament formation. While MamK is closest in sequence to the bacterial actin MreB, the longitudinal contacts along each MamK strand most closely resemble those of eukaryotic actin. In contrast, the cross-strand interface, with a surprisingly limited set of contacts, is novel among actin homologs and gives rise to the nonstaggered architecture.
Insights
Magnetotactic bacteria use MamK protein filaments to align internal magnetosomes for magnetic sensing. Cryo-EM reveals MamK filament structure, showing unique contacts distinct from other actin homologs.
Area of Science:
- Microbiology
- Structural Biology
- Biophysics
Background:
- Magnetotactic bacteria navigate using intracellular magnetic crystals (magnetosomes).
- Proper magnetosome alignment is crucial for bacterial magnetic sensing and navigation.
- MamK protein filaments are known to anchor magnetosomes within the bacterial cell.
Purpose of the Study:
- To determine the high-resolution structure of the MamK filament.
- To elucidate the molecular basis of MamK filament assembly and architecture.
- To compare MamK structure and contacts with other actin homologs.
Main Methods:
- Cryo-electron microscopy (cryo-EM) was used to obtain the MamK filament structure at approximately 6.5 Å resolution.
- Structural analysis focused on identifying inter-protein contacts and overall filament architecture.
Main Results:
- The MamK filament adopts a double-stranded, non-staggered architecture.
- Longitudinal contacts within each strand resemble eukaryotic actin, while cross-strand contacts are novel.
- The unique cross-strand interface explains the non-staggered filament arrangement.
Conclusions:
- The determined cryo-EM structure reveals the molecular details of MamK filament formation.
- MamK filaments exhibit a unique structural organization distinct from other known actin homologs like MreB.
- This structural insight provides a foundation for understanding magnetosome-cytoskeleton interactions in magnetotactic bacteria.
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