Cargando…

Atomic-level architecture of Caulobacter crescentus flagellar filaments provide evidence for multi-flagellin filament stabilization

Flagella are dynamic, ion-powered machines with assembly pathways that are optimized for efficient flagella production. In bacteria, dozens of genes are coordinated at specific times in the cell lifecycle to generate each component of the flagellum. This is the case for Caulobacter crescentus, but l...

Descripción completa

Detalles Bibliográficos
Autores principales: Sanchez, Juan C., Montemayor, Eric J., Ploscariu, Nicoleta T., Parrell, Daniel, Baumgardt, Joseph K., Yang, Jie E., Sibert, Bryan, Cai, Kai, Wright, Elizabeth R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10369909/
https://www.ncbi.nlm.nih.gov/pubmed/37503001
http://dx.doi.org/10.1101/2023.07.10.548443
_version_ 1785077858413051904
author Sanchez, Juan C.
Montemayor, Eric J.
Ploscariu, Nicoleta T.
Parrell, Daniel
Baumgardt, Joseph K.
Yang, Jie E.
Sibert, Bryan
Cai, Kai
Wright, Elizabeth R.
author_facet Sanchez, Juan C.
Montemayor, Eric J.
Ploscariu, Nicoleta T.
Parrell, Daniel
Baumgardt, Joseph K.
Yang, Jie E.
Sibert, Bryan
Cai, Kai
Wright, Elizabeth R.
author_sort Sanchez, Juan C.
collection PubMed
description Flagella are dynamic, ion-powered machines with assembly pathways that are optimized for efficient flagella production. In bacteria, dozens of genes are coordinated at specific times in the cell lifecycle to generate each component of the flagellum. This is the case for Caulobacter crescentus, but little is known about why this species encodes six different flagellin genes. Furthermore, little is known about the benefits multi-flagellin species possess over single flagellin species, if any, or what molecular properties allow for multi-flagellin filaments to assemble. Here we present an in-depth analysis of several single flagellin filaments from C. crescentus, including an extremely well-resolved structure of a bacterial flagellar filament. We highlight key molecular interactions that differ between each bacterial strain and speculate how these interactions may alleviate or impose helical strain on the overall architecture of the filament. We detail conserved residues within the flagellin subunit that allow for the synthesis of multi-flagellin filaments. We further comment on how these molecular differences impact bacterial motility and highlight how no single flagellin filament achieves wild-type levels of motility, suggesting C. crescentus has evolved to produce a filament optimized for motility comprised of six flagellins. Finally, we highlight an ordered arrangement of glycosylation sites on the surface of the filaments and speculate how these sites may protect the β-hairpin located on the surface exposed domain of the flagellin subunit.
format Online
Article
Text
id pubmed-10369909
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Cold Spring Harbor Laboratory
record_format MEDLINE/PubMed
spelling pubmed-103699092023-07-27 Atomic-level architecture of Caulobacter crescentus flagellar filaments provide evidence for multi-flagellin filament stabilization Sanchez, Juan C. Montemayor, Eric J. Ploscariu, Nicoleta T. Parrell, Daniel Baumgardt, Joseph K. Yang, Jie E. Sibert, Bryan Cai, Kai Wright, Elizabeth R. bioRxiv Article Flagella are dynamic, ion-powered machines with assembly pathways that are optimized for efficient flagella production. In bacteria, dozens of genes are coordinated at specific times in the cell lifecycle to generate each component of the flagellum. This is the case for Caulobacter crescentus, but little is known about why this species encodes six different flagellin genes. Furthermore, little is known about the benefits multi-flagellin species possess over single flagellin species, if any, or what molecular properties allow for multi-flagellin filaments to assemble. Here we present an in-depth analysis of several single flagellin filaments from C. crescentus, including an extremely well-resolved structure of a bacterial flagellar filament. We highlight key molecular interactions that differ between each bacterial strain and speculate how these interactions may alleviate or impose helical strain on the overall architecture of the filament. We detail conserved residues within the flagellin subunit that allow for the synthesis of multi-flagellin filaments. We further comment on how these molecular differences impact bacterial motility and highlight how no single flagellin filament achieves wild-type levels of motility, suggesting C. crescentus has evolved to produce a filament optimized for motility comprised of six flagellins. Finally, we highlight an ordered arrangement of glycosylation sites on the surface of the filaments and speculate how these sites may protect the β-hairpin located on the surface exposed domain of the flagellin subunit. Cold Spring Harbor Laboratory 2023-07-10 /pmc/articles/PMC10369909/ /pubmed/37503001 http://dx.doi.org/10.1101/2023.07.10.548443 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Sanchez, Juan C.
Montemayor, Eric J.
Ploscariu, Nicoleta T.
Parrell, Daniel
Baumgardt, Joseph K.
Yang, Jie E.
Sibert, Bryan
Cai, Kai
Wright, Elizabeth R.
Atomic-level architecture of Caulobacter crescentus flagellar filaments provide evidence for multi-flagellin filament stabilization
title Atomic-level architecture of Caulobacter crescentus flagellar filaments provide evidence for multi-flagellin filament stabilization
title_full Atomic-level architecture of Caulobacter crescentus flagellar filaments provide evidence for multi-flagellin filament stabilization
title_fullStr Atomic-level architecture of Caulobacter crescentus flagellar filaments provide evidence for multi-flagellin filament stabilization
title_full_unstemmed Atomic-level architecture of Caulobacter crescentus flagellar filaments provide evidence for multi-flagellin filament stabilization
title_short Atomic-level architecture of Caulobacter crescentus flagellar filaments provide evidence for multi-flagellin filament stabilization
title_sort atomic-level architecture of caulobacter crescentus flagellar filaments provide evidence for multi-flagellin filament stabilization
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10369909/
https://www.ncbi.nlm.nih.gov/pubmed/37503001
http://dx.doi.org/10.1101/2023.07.10.548443
work_keys_str_mv AT sanchezjuanc atomiclevelarchitectureofcaulobactercrescentusflagellarfilamentsprovideevidenceformultiflagellinfilamentstabilization
AT montemayorericj atomiclevelarchitectureofcaulobactercrescentusflagellarfilamentsprovideevidenceformultiflagellinfilamentstabilization
AT ploscariunicoletat atomiclevelarchitectureofcaulobactercrescentusflagellarfilamentsprovideevidenceformultiflagellinfilamentstabilization
AT parrelldaniel atomiclevelarchitectureofcaulobactercrescentusflagellarfilamentsprovideevidenceformultiflagellinfilamentstabilization
AT baumgardtjosephk atomiclevelarchitectureofcaulobactercrescentusflagellarfilamentsprovideevidenceformultiflagellinfilamentstabilization
AT yangjiee atomiclevelarchitectureofcaulobactercrescentusflagellarfilamentsprovideevidenceformultiflagellinfilamentstabilization
AT sibertbryan atomiclevelarchitectureofcaulobactercrescentusflagellarfilamentsprovideevidenceformultiflagellinfilamentstabilization
AT caikai atomiclevelarchitectureofcaulobactercrescentusflagellarfilamentsprovideevidenceformultiflagellinfilamentstabilization
AT wrightelizabethr atomiclevelarchitectureofcaulobactercrescentusflagellarfilamentsprovideevidenceformultiflagellinfilamentstabilization