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Dr Catherine Abbott

Contact Details

     Phone: +61 8 8201 2078
     Fax: +61 8 8201 3015
     Email: cathy.abbott@flinders.edu.au
     Location:  Room 333/333a, Biological Sciences building (building 51)

Key Responsibilities

  • Course Coordinator for Bachelor of Science in Bioinformatics (Extended Major in Bioinformatics), (Major in Molecular Biology)
    Abbott lab members  
    Abbott lab members at ASMR gala dinner 2007  
  • Topic Coordinator for BIOL2241, BIOL3175, BIOL3185, BIOL2220

Teaching

  • Bioinformatics
  • Molecular Biology
  • Molecular Cell Biology
  • Functional Genomics

Research

My current research focuses on a family of peptidases that are interesting due their heightened expression by activated cells, particularly T cells and hepatic stellate cells, their involvement in cell-extracellular matrix (ECM) interactions and their roles in leukocyte chemotaxis, T cell proliferation, HIV infection and tumor growth (McCaughan et al 2000).

Dipeptidyl Peptidase IV (DPPIV)/CD26 is a multifunctional protein which has three unique biological functions (1) an enzyme activity (2) binding to adenosine deaminase (ADA) and (3) T cell activation. The expression of DPPIV on the lymphocyte surface is important for lymphocyte function and in the pathogenesis of the human immunodeficiency virus (HIV). Three other DPPIV-like proteins, with significant sequence homology have been cloned: DPPX-l, DPPX-s and fibroblast activation protein (FAP). The DPPX proteins are expressed in the brain and are thought to be involved in signalling processes. FAP has been shown to be important in the pathogenesis of both cancer and cirrhosis of the liver . The identification of these molecules suggests the existence of a highly specialized DPPIV-like gene family in which members will probably share gene structure, three-dimensional protein structure and perhaps functions.

Recently we have cloned novel members of this gene family (Abbott et al 2000a&b). Honours projects in this lab will involve further biochemical characterization of these new proteins and examination of the role of these proteins in human disease.

Long term Goal of this research: The discovery of novel DPPIV-like genes will lead to increased understanding of the role of this emerging family in the immune system and in disease pathogenesis. In addition, the discovery of new genes may lead to new targets and inhibitor based therapies for the treatment of such diseases as diabetes, obesity, inflammation of the bowel and HIV.

See publication list

Other Professional

Memberships of Boards and other duties

ANGIS and AGIC board 2001-2003

2005-2006

Adelaide Women’s and Children’s Hospital Research Committee 2003-2005
Bioinformatics Australia Board 2004-2006
Vice President, Bioinformatics Australia Board 2005-2007
   
Member of the following societies
Gastroenterological Society of Australia 1993-2007
Australian Society for Biochemistry and Molecular Biology 1997-2007
Australian Society for Medical Research 2002-2007
  · member of State Branch Committee 2002-2005
  · co-convenor of the 2002 State Branch Conference
  · member of the program committee 2003 National conference
International Proteolysis Society (IPS) 2001-2006
International Society of Computational Biology (ISCB) 2001-2006
  · member of ISCB Education Committee
AusBiotech-Bioinformatics Australia 2004-2007

Current PhD students


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