Curvature Generation and Engineering Principles from Shewanella Oneidensis Multi-Flagellin Flagellum. Lou, Q., Fan, H., Liu, Y., Miller, J. F., Huang, Y., & Zhou, Z. H. February, 2025. doi abstract bibtex Motility driven by nanoscale flagella is vital to microbial survival and spread in fluid and structured environments. Absence of native flagellum structures, however, has limited our understanding of the mechanisms of microbial motility, hindering efforts to engineer microbe-based microbots for applications. Here, by cryogenic electron tomography (cryoET) and microscopy (cryoEM), we determined the structural basis of motility driven by the single flagellum anchored to one pole of Shewanella oneidensis MR-1 (S. oneidensis), an electrogenic bacterium commonly used in biotechnology. The structures of the curved flagellum, representing the conformation during motion, are captured, allowing delineation of molecular interactions among the subunits of its three components—filament, hook, and hook-filament junction. The structures of the filament, i.e., the propeller, reveal a varying composition of the flagellin isoforms FlaA and FlaB throughout the filament. Distinct inter-subunit interactions are identified at residues 129 and 134, which are the major determinants of functional differences in motility for the two isoforms. The hook—the universal joint—has a significantly larger curvature than that of the filament, despite both containing 11 curvature-defining conformers of their subunits. Transition between the propeller and universal joint is mediated by hook-filament junction, composed of 11 subunits of FlgK and FlgL, reconciling incompatibility between the filament and hook. Correlating these compositional and structural transitions with varying levels of curvature in flagellar segments reveals molecular mechanism enabling propulsive motility. Mechanistic understandings from S. oneidensis suggest engineering principles for nanoscale biomimetic systems. $<$img class="highwire-fragment fragment-image" alt="Figure" src="https://www.biorxiv.org/content/biorxiv/early/2025/02/08/2025.02.07.637127/F1.medium.gif" width="440" height="293"/$>$Download figureOpen in new tab
@misc{louCurvatureGenerationEngineering2025,
title = {Curvature Generation and Engineering Principles from {{Shewanella}} Oneidensis Multi-Flagellin Flagellum},
author = {Lou, Qing and Fan, Hongcheng and Liu, Yang and Miller, Jeff F. and Huang, Yu and Zhou, Z. Hong},
year = {2025},
month = feb,
primaryclass = {New Results},
pages = {2025.02.07.637127},
publisher = {bioRxiv},
doi = {10.1101/2025.02.07.637127},
urldate = {2025-04-04},
abstract = {Motility driven by nanoscale flagella is vital to microbial survival and spread in fluid and structured environments. Absence of native flagellum structures, however, has limited our understanding of the mechanisms of microbial motility, hindering efforts to engineer microbe-based microbots for applications. Here, by cryogenic electron tomography (cryoET) and microscopy (cryoEM), we determined the structural basis of motility driven by the single flagellum anchored to one pole of Shewanella oneidensis MR-1 (S. oneidensis), an electrogenic bacterium commonly used in biotechnology. The structures of the curved flagellum, representing the conformation during motion, are captured, allowing delineation of molecular interactions among the subunits of its three components---filament, hook, and hook-filament junction. The structures of the filament, i.e., the propeller, reveal a varying composition of the flagellin isoforms FlaA and FlaB throughout the filament. Distinct inter-subunit interactions are identified at residues 129 and 134, which are the major determinants of functional differences in motility for the two isoforms. The hook---the universal joint---has a significantly larger curvature than that of the filament, despite both containing 11 curvature-defining conformers of their subunits. Transition between the propeller and universal joint is mediated by hook-filament junction, composed of 11 subunits of FlgK and FlgL, reconciling incompatibility between the filament and hook. Correlating these compositional and structural transitions with varying levels of curvature in flagellar segments reveals molecular mechanism enabling propulsive motility. Mechanistic understandings from S. oneidensis suggest engineering principles for nanoscale biomimetic systems. {$<$}img class="highwire-fragment fragment-image" alt="Figure" src="https://www.biorxiv.org/content/biorxiv/early/2025/02/08/2025.02.07.637127/F1.medium.gif" width="440" height="293"/{$>$}Download figureOpen in new tab},
archiveprefix = {bioRxiv},
chapter = {New Results},
copyright = {{\copyright} 2025, Posted by Cold Spring Harbor Laboratory. This pre-print is available under a Creative Commons License (Attribution 4.0 International), CC BY 4.0, as described at http://creativecommons.org/licenses/by/4.0/},
langid = {english},
file = {C:\Users\shervinnia\Zotero\storage\EXJFR9KW\Lou et al. - 2025 - Curvature generation and engineering principles from Shewanella oneidensis multi-flagellin flagellum.pdf}
}
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H."],"bibdata":{"bibtype":"misc","type":"misc","title":"Curvature Generation and Engineering Principles from Shewanella Oneidensis Multi-Flagellin Flagellum","author":[{"propositions":[],"lastnames":["Lou"],"firstnames":["Qing"],"suffixes":[]},{"propositions":[],"lastnames":["Fan"],"firstnames":["Hongcheng"],"suffixes":[]},{"propositions":[],"lastnames":["Liu"],"firstnames":["Yang"],"suffixes":[]},{"propositions":[],"lastnames":["Miller"],"firstnames":["Jeff","F."],"suffixes":[]},{"propositions":[],"lastnames":["Huang"],"firstnames":["Yu"],"suffixes":[]},{"propositions":[],"lastnames":["Zhou"],"firstnames":["Z.","Hong"],"suffixes":[]}],"year":"2025","month":"February","primaryclass":"New Results","pages":"2025.02.07.637127","publisher":"bioRxiv","doi":"10.1101/2025.02.07.637127","urldate":"2025-04-04","abstract":"Motility driven by nanoscale flagella is vital to microbial survival and spread in fluid and structured environments. Absence of native flagellum structures, however, has limited our understanding of the mechanisms of microbial motility, hindering efforts to engineer microbe-based microbots for applications. Here, by cryogenic electron tomography (cryoET) and microscopy (cryoEM), we determined the structural basis of motility driven by the single flagellum anchored to one pole of Shewanella oneidensis MR-1 (S. oneidensis), an electrogenic bacterium commonly used in biotechnology. The structures of the curved flagellum, representing the conformation during motion, are captured, allowing delineation of molecular interactions among the subunits of its three components—filament, hook, and hook-filament junction. The structures of the filament, i.e., the propeller, reveal a varying composition of the flagellin isoforms FlaA and FlaB throughout the filament. Distinct inter-subunit interactions are identified at residues 129 and 134, which are the major determinants of functional differences in motility for the two isoforms. The hook—the universal joint—has a significantly larger curvature than that of the filament, despite both containing 11 curvature-defining conformers of their subunits. Transition between the propeller and universal joint is mediated by hook-filament junction, composed of 11 subunits of FlgK and FlgL, reconciling incompatibility between the filament and hook. Correlating these compositional and structural transitions with varying levels of curvature in flagellar segments reveals molecular mechanism enabling propulsive motility. Mechanistic understandings from S. oneidensis suggest engineering principles for nanoscale biomimetic systems. $<$img class=\"highwire-fragment fragment-image\" alt=\"Figure\" src=\"https://www.biorxiv.org/content/biorxiv/early/2025/02/08/2025.02.07.637127/F1.medium.gif\" width=\"440\" height=\"293\"/$>$Download figureOpen in new tab","archiveprefix":"bioRxiv","chapter":"New Results","copyright":"© 2025, Posted by Cold Spring Harbor Laboratory. 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Absence of native flagellum structures, however, has limited our understanding of the mechanisms of microbial motility, hindering efforts to engineer microbe-based microbots for applications. Here, by cryogenic electron tomography (cryoET) and microscopy (cryoEM), we determined the structural basis of motility driven by the single flagellum anchored to one pole of Shewanella oneidensis MR-1 (S. oneidensis), an electrogenic bacterium commonly used in biotechnology. The structures of the curved flagellum, representing the conformation during motion, are captured, allowing delineation of molecular interactions among the subunits of its three components---filament, hook, and hook-filament junction. The structures of the filament, i.e., the propeller, reveal a varying composition of the flagellin isoforms FlaA and FlaB throughout the filament. Distinct inter-subunit interactions are identified at residues 129 and 134, which are the major determinants of functional differences in motility for the two isoforms. The hook---the universal joint---has a significantly larger curvature than that of the filament, despite both containing 11 curvature-defining conformers of their subunits. Transition between the propeller and universal joint is mediated by hook-filament junction, composed of 11 subunits of FlgK and FlgL, reconciling incompatibility between the filament and hook. Correlating these compositional and structural transitions with varying levels of curvature in flagellar segments reveals molecular mechanism enabling propulsive motility. 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