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9FLP

CryoEM structure of the neck (1403-2314) in the grappling hook protein A (GhpA) in the bacterium Aureispira sp. CCB-QB1

Summary for 9FLP
Entry DOI10.2210/pdb9flp/pdb
EMDB information50537
DescriptorThe grappling hook protein A in the bacterium Aureispira sp. CCB-QB1 (1 entity in total)
Functional Keywordsixotrophy, type 9 secretion system, cryoem, surface protein, predation, cell adhesion
Biological sourceAureispira sp. CCB-QB1
Total number of polymer chains7
Total formula weight4270800.63
Authors
Lien, Y.-W.,Amendola, D.,Lee, K.S.,Bartlau, N.,Xu, J.,Furusawa, G.,Polz, M.F.,Stocker, R.,Weiss, G.L.,Pilhofer, M. (deposition date: 2024-06-05, release date: 2024-10-16, Last modification date: 2024-10-30)
Primary citationLien, Y.W.,Amendola, D.,Lee, K.S.,Bartlau, N.,Xu, J.,Furusawa, G.,Polz, M.F.,Stocker, R.,Weiss, G.L.,Pilhofer, M.
Mechanism of bacterial predation via ixotrophy.
Science, 386:eadp0614-eadp0614, 2024
Cited by
PubMed Abstract: Ixotrophy is a contact-dependent predatory strategy of filamentous bacteria in aquatic environments for which the molecular mechanism remains unknown. We show that predator-prey contact can be established by gliding motility or extracellular assemblages we call "grappling hooks." Cryo-electron microscopy identified the grappling hooks as heptamers of a type IX secretion system substrate. After close predator-prey contact is established, cryo-electron tomography and functional assays showed that puncturing by a type VI secretion system mediated killing. Single-cell analyses with stable isotope-labeled prey revealed that prey components are taken up by the attacker. Depending on nutrient availability, insertion sequence elements toggle the activity of ixotrophy. A marine metagenomic time series shows coupled dynamics of ixotrophic bacteria and prey. We found that the mechanism of ixotrophy involves multiple cellular machineries, is conserved, and may shape microbial populations in the environment.
PubMed: 39418385
DOI: 10.1126/science.adp0614
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.8 Å)
Structure validation

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