Kafatos:Stathopoulos, Stavros: Difference between revisions

From OpenWetWare
Jump to navigationJump to search
No edit summary
 
(2 intermediate revisions by the same user not shown)
Line 76: Line 76:
==Publications==
==Publications==
<!-- Replace the PubMed ID's ("pmid=#######") below with the PubMed ID's for your publications.  You can add or remove lines as needed -->
<!-- Replace the PubMed ID's ("pmid=#######") below with the PubMed ID's for your publications.  You can add or remove lines as needed -->
<biblio>
<biblio>
#P pmid=20004161
 
#P pmid=20439706
#2 pmid=21044884
#2 pmid=20439706
#3 pmid=20004161
 





Latest revision as of 15:12, 15 November 2010

Click here to visit our NEW WEBSITE
The content below is most likely out of date. We also have a new lean and mean openwetware area.


Stavros Stathopoulos

Division of Cell & Molecular Biology,
South Kensington Campus, SAF building,
London,
SW7 2AZ,
UK


stavros.stathopoulos07#imperial.ac.uk

Tel: +44 (0) 20 7594 5361
Fax: +44 (0) 20 7584 2056



I am a PhD candidate in the Kafatos/Christophides lab at Imperial College London.



Education

  • 2009, MRes, Molecular & Cellular Basis of Infection, Imperial College London
  • 2008, MRes, Biomedical Research, Imperial College London
  • 2005, BSc, Biology, University of Crete

Research interests

My project explores the tripartite interactions between the mosquito gut microbial communities, the PGRPLC-mediated anti-bacterial defence reactions and infections with Plasmodium, and how these might be exploited in future interventions aiming to control malaria transmission. Bacteria in the mosquito midgut have been previously shown to affect Plasmodium development. The dramatic bacterial proliferation after a blood meal coincides with the invasion of the mosquito midgut by Plasmodium ookinetes, with An. gambiae immune responses to limit bacterial proliferation affecting the infection intensity of human and rodent Plasmodium parasites. The aim of the project is to investigate the diversity and dynamics of the mosquito gut microbiota, elucidate constitutive immune responses triggered by commensal bacteria that may affect susceptibility and refractoriness against Plasmodium infections, characterize bacterial populations responsible for inducible immunity and explore the possibility of the use of genetically modified bacteria for blocking malaria transmission.

 

Publications

  1. Xu H, Raynal N, Stathopoulos S, Myllyharju J, Farndale RW, and Leitinger B. Collagen binding specificity of the discoidin domain receptors: binding sites on collagens II and III and molecular determinants for collagen IV recognition by DDR1. Matrix Biol. 2011 Jan;30(1):16-26. DOI:10.1016/j.matbio.2010.10.004 | PubMed ID:21044884 | HubMed [2]
  2. Fadda L, Borhis G, Ahmed P, Cheent K, Pageon SV, Cazaly A, Stathopoulos S, Middleton D, Mulder A, Claas FH, Elliott T, Davis DM, Purbhoo MA, and Khakoo SI. Peptide antagonism as a mechanism for NK cell activation. Proc Natl Acad Sci U S A. 2010 Jun 1;107(22):10160-5. DOI:10.1073/pnas.0913745107 | PubMed ID:20439706 | HubMed [2]
  3. Carafoli F, Bihan D, Stathopoulos S, Konitsiotis AD, Kvansakul M, Farndale RW, Leitinger B, and Hohenester E. Crystallographic insight into collagen recognition by discoidin domain receptor 2. Structure. 2009 Dec 9;17(12):1573-1581. DOI:10.1016/j.str.2009.10.012 | PubMed ID:20004161 | HubMed [3]
All Medline abstracts: PubMed | HubMed

Useful links