Cargando…

Cooperative Retraction of Bundled Type IV Pili Enables Nanonewton Force Generation

The causative agent of gonorrhea, Neisseria gonorrhoeae, bears retractable filamentous appendages called type IV pili (Tfp). Tfp are used by many pathogenic and nonpathogenic bacteria to carry out a number of vital functions, including DNA uptake, twitching motility (crawling over surfaces), and att...

Descripción completa

Detalles Bibliográficos
Autores principales: Biais, Nicolas, Ladoux, Benoît, Higashi, Dustin, So, Magdalene, Sheetz, Michael
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2292754/
https://www.ncbi.nlm.nih.gov/pubmed/18416602
http://dx.doi.org/10.1371/journal.pbio.0060087
_version_ 1782152526596931584
author Biais, Nicolas
Ladoux, Benoît
Higashi, Dustin
So, Magdalene
Sheetz, Michael
author_facet Biais, Nicolas
Ladoux, Benoît
Higashi, Dustin
So, Magdalene
Sheetz, Michael
author_sort Biais, Nicolas
collection PubMed
description The causative agent of gonorrhea, Neisseria gonorrhoeae, bears retractable filamentous appendages called type IV pili (Tfp). Tfp are used by many pathogenic and nonpathogenic bacteria to carry out a number of vital functions, including DNA uptake, twitching motility (crawling over surfaces), and attachment to host cells. In N. gonorrhoeae, Tfp binding to epithelial cells and the mechanical forces associated with this binding stimulate signaling cascades and gene expression that enhance infection. Retraction of a single Tfp filament generates forces of 50–100 piconewtons, but nothing is known, thus far, on the retraction force ability of multiple Tfp filaments, even though each bacterium expresses multiple Tfp and multiple bacteria interact during infection. We designed a micropillar assay system to measure Tfp retraction forces. This system consists of an array of force sensors made of elastic pillars that allow quantification of retraction forces from adherent N. gonorrhoeae bacteria. Electron microscopy and fluorescence microscopy were used in combination with this novel assay to assess the structures of Tfp. We show that Tfp can form bundles, which contain up to 8–10 Tfp filaments, that act as coordinated retractable units with forces up to 10 times greater than single filament retraction forces. Furthermore, single filament retraction forces are transient, whereas bundled filaments produce retraction forces that can be sustained. Alterations of noncovalent protein–protein interactions between Tfp can inhibit both bundle formation and high-amplitude retraction forces. Retraction forces build over time through the recruitment and bundling of multiple Tfp that pull cooperatively to generate forces in the nanonewton range. We propose that Tfp retraction can be synchronized through bundling, that Tfp bundle retraction can generate forces in the nanonewton range in vivo, and that such high forces could affect infection.
format Text
id pubmed-2292754
institution National Center for Biotechnology Information
language English
publishDate 2008
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-22927542008-04-15 Cooperative Retraction of Bundled Type IV Pili Enables Nanonewton Force Generation Biais, Nicolas Ladoux, Benoît Higashi, Dustin So, Magdalene Sheetz, Michael PLoS Biol Research Article The causative agent of gonorrhea, Neisseria gonorrhoeae, bears retractable filamentous appendages called type IV pili (Tfp). Tfp are used by many pathogenic and nonpathogenic bacteria to carry out a number of vital functions, including DNA uptake, twitching motility (crawling over surfaces), and attachment to host cells. In N. gonorrhoeae, Tfp binding to epithelial cells and the mechanical forces associated with this binding stimulate signaling cascades and gene expression that enhance infection. Retraction of a single Tfp filament generates forces of 50–100 piconewtons, but nothing is known, thus far, on the retraction force ability of multiple Tfp filaments, even though each bacterium expresses multiple Tfp and multiple bacteria interact during infection. We designed a micropillar assay system to measure Tfp retraction forces. This system consists of an array of force sensors made of elastic pillars that allow quantification of retraction forces from adherent N. gonorrhoeae bacteria. Electron microscopy and fluorescence microscopy were used in combination with this novel assay to assess the structures of Tfp. We show that Tfp can form bundles, which contain up to 8–10 Tfp filaments, that act as coordinated retractable units with forces up to 10 times greater than single filament retraction forces. Furthermore, single filament retraction forces are transient, whereas bundled filaments produce retraction forces that can be sustained. Alterations of noncovalent protein–protein interactions between Tfp can inhibit both bundle formation and high-amplitude retraction forces. Retraction forces build over time through the recruitment and bundling of multiple Tfp that pull cooperatively to generate forces in the nanonewton range. We propose that Tfp retraction can be synchronized through bundling, that Tfp bundle retraction can generate forces in the nanonewton range in vivo, and that such high forces could affect infection. Public Library of Science 2008-04 2008-04-15 /pmc/articles/PMC2292754/ /pubmed/18416602 http://dx.doi.org/10.1371/journal.pbio.0060087 Text en © 2008 Biais et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Biais, Nicolas
Ladoux, Benoît
Higashi, Dustin
So, Magdalene
Sheetz, Michael
Cooperative Retraction of Bundled Type IV Pili Enables Nanonewton Force Generation
title Cooperative Retraction of Bundled Type IV Pili Enables Nanonewton Force Generation
title_full Cooperative Retraction of Bundled Type IV Pili Enables Nanonewton Force Generation
title_fullStr Cooperative Retraction of Bundled Type IV Pili Enables Nanonewton Force Generation
title_full_unstemmed Cooperative Retraction of Bundled Type IV Pili Enables Nanonewton Force Generation
title_short Cooperative Retraction of Bundled Type IV Pili Enables Nanonewton Force Generation
title_sort cooperative retraction of bundled type iv pili enables nanonewton force generation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2292754/
https://www.ncbi.nlm.nih.gov/pubmed/18416602
http://dx.doi.org/10.1371/journal.pbio.0060087
work_keys_str_mv AT biaisnicolas cooperativeretractionofbundledtypeivpilienablesnanonewtonforcegeneration
AT ladouxbenoit cooperativeretractionofbundledtypeivpilienablesnanonewtonforcegeneration
AT higashidustin cooperativeretractionofbundledtypeivpilienablesnanonewtonforcegeneration
AT somagdalene cooperativeretractionofbundledtypeivpilienablesnanonewtonforcegeneration
AT sheetzmichael cooperativeretractionofbundledtypeivpilienablesnanonewtonforcegeneration