Three‐dimensional electron microscopy reconstruction and cysteine‐mediated crosslinking provide a model of the type III secretion system needle tip complex. Issue 1 (27th November 2014)
- Record Type:
- Journal Article
- Title:
- Three‐dimensional electron microscopy reconstruction and cysteine‐mediated crosslinking provide a model of the type III secretion system needle tip complex. Issue 1 (27th November 2014)
- Main Title:
- Three‐dimensional electron microscopy reconstruction and cysteine‐mediated crosslinking provide a model of the type III secretion system needle tip complex
- Authors:
- Cheung, Martin
Shen, Da‐Kang
Makino, Fumiaki
Kato, Takayuki
Roehrich, A. Dorothea
Martinez‐Argudo, Isabel
Walker, Matthew L.
Murillo, Isabel
Liu, Xia
Pain, Maria
Brown, James
Frazer, Gordon
Mantell, Judith
Mina, Petros
Todd, Thomas
Sessions, Richard B.
Namba, Keiichi
Blocker, Ariel J. - Abstract:
- <abstract abstract-type="main"> <title>Summary</title> <p>Type III secretion systems are found in many Gram‐negative bacteria. They are activated by contact with eukaryotic cells and inject virulence proteins inside them. Host cell detection requires a protein complex located at the tip of the device's external injection needle. The <italic>Shigella</italic> tip complex (TC) is composed of IpaD, a hydrophilic protein, and IpaB, a hydrophobic protein, which later forms part of the injection pore in the host membrane. Here we used labelling and crosslinking methods to show that TCs from a Δ<italic>ipaB</italic> strain contain five IpaD subunits while the TCs from wild‐type can also contain one IpaB and four IpaD subunits. Electron microscopy followed by single particle and helical image analysis was used to reconstruct three‐dimensional images of TCs at ∼20 Å resolution. Docking of an IpaD crystal structure, constrained by the crosslinks observed, reveals that TC organisation is different from that of all previously proposed models. Our findings suggest new mechanisms for TC assembly and function. The TC is the only site within these secretion systems targeted by disease‐protecting antibodies. By suggesting how these act, our work will allow improvement of prophylactic and therapeutic strategies.</p> </abstract>
- Is Part Of:
- Molecular microbiology. Volume 95:Issue 1(2015)
- Journal:
- Molecular microbiology
- Issue:
- Volume 95:Issue 1(2015)
- Issue Display:
- Volume 95, Issue 1 (2015)
- Year:
- 2015
- Volume:
- 95
- Issue:
- 1
- Issue Sort Value:
- 2015-0095-0001-0000
- Page Start:
- 31
- Page End:
- 50
- Publication Date:
- 2014-11-27
- Subjects:
- Molecular microbiology -- Periodicals
572.829 - Journal URLs:
- http://www.blackwell-synergy.com/servlet/useragent?func=showIssues&code=mmi&close=2003#C2003 ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1365-2958 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/mmi.12843 ↗
- Languages:
- English
- ISSNs:
- 0950-382X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5900.817960
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3056.xml