Donor strand complementation and calcium ion coordination drive the chaperone-free polymerization of archaeal cannulae

Cannulae are structurally rigid tubular protein filaments that accumulate on the extracellular surface of archaea within the family Pyrodictiaceae during cell growth. These obligate anaerobes propagate under hyperthermophilic conditions in which cannulae form a biomatrix that interconnects and sustains cells. The persistence of cannulae in this environment suggests that these filaments display significant thermostability, which has attracted technological interest in their development as synthetic protein-based biomaterials. Here, we report cryoEM structural analyses of ex vivo and in vitro assembled recombinant cannulae. We demonstrate that the interactions between protomers in native and recombinant cannulae is based on donor strand complementation (DSC), a form of non-covalent polymerization previously observed for bacterial chaperone-usher pili. Unexpectedly, calcium ion coordination at the subunit interfaces reinforces the network of donor strand interactions in the cannulae. This study provides insight into the mechanism of assembly of cannulae and the structural origin of their high stability and rigidity.

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Publication Details

Journal
Nature Communications
Published
2025-10-13
DOI
https://doi.org/10.1038/s41467-025-64120-8
Citations
3
Primary Topic
Enzyme Structure and Function
Type
article
Field-Weighted Citation Impact
1.55
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article

Donor strand complementation and calcium ion coordination drive the chaperone-free polymerization of archaeal cannulae

Vincent P. Conticello, Vikram Alva, Edward H. Egelman, Mike Sleutel et al.
3 citations
Nature Communications
Enzyme Structure and Function
1.55
article

Donor strand complementation and calcium ion coordination drive the chaperone-free polymerization of archaeal cannulae

Vincent P. Conticello, Vikram Alva, Edward H. Egelman, Mike Sleutel, Han Remaut, Andres Gonzalez Socorro, Ravi R. Sonani, Borries Demeler, Fengbin Wang, Jessalyn Miller, Yang Chen, M. Rudolph, R. Bruce Martin
article en
3 citations

Abstract

Cannulae are structurally rigid tubular protein filaments that accumulate on the extracellular surface of archaea within the family Pyrodictiaceae during cell growth. These obligate anaerobes propagate under hyperthermophilic conditions in which cannulae form a biomatrix that interconnects and sustains cells. The persistence of cannulae in this environment suggests that these filaments display significant thermostability, which has attracted technological interest in their development as synthetic protein-based biomaterials. Here, we report cryoEM structural analyses of ex vivo and in vitro assembled recombinant cannulae. We demonstrate that the interactions between protomers in native and recombinant cannulae is based on donor strand complementation (DSC), a form of non-covalent polymerization previously observed for bacterial chaperone-usher pili. Unexpectedly, calcium ion coordination at the subunit interfaces reinforces the network of donor strand interactions in the cannulae. This study provides insight into the mechanism of assembly of cannulae and the structural origin of their high stability and rigidity.

Nature CommunicationsVol. 16(1)
University of Lethbridge (CA), Vrije Universiteit Brussel (BE), Emory University (US), University of Alabama at Birmingham (US), New York Structural Biology Center (US), VIB-VUB Center for Structural Biology (BE), Max Planck Institute for Biology (DE), University of Virginia (US)
Openalex Percentile: Top 16%
Enzyme Structure and Function
1.55
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