(provide by applicant): Identifying the fundamental mechanisms and components of protein trafficking in trypanosomes is critical for understanding the interaction of this parasite with its host. The development of systems for introducing and expressing heterologous genes in trypanosomes allows investigations at the molecular level of the factors mediating endocytic and exocytic processes. The recent identification of a lysozme membrane glycoprotein, p67, from the African trypanosome, T. brucei, and a homolog in the related South American trypanosome, T. cruzi, should by analogy to vertebrate lysosome proteins enable the identification of the cytosolic components required for cargo loading and vesicle formation. The innate targeting signals in p67 will be delineated and subsequently used to purify and clone the cytoplasmic constituents that mediate lysosome targeting of this membrane glycoprotein. Reporters will be constructed that are targeted to the lysosome by fusion with the cytoplasmic domain that mediates targeting. This domain will also be used as bait in both biochemical (affinity purification) and genetic (yeast two-hybrid analysis) approaches to isolate p67CD-binding protein. These cytosolic proteins can be expected to function in cargo loading and vesicle formation and thus be critical for secretory and endocytic protein trafficking in trypanosomes.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32AI010552-03
Application #
6423065
Study Section
Special Emphasis Panel (ZRG1-TMP (01))
Program Officer
Wali, Tonu M
Project Start
2002-02-01
Project End
Budget Start
2002-02-01
Budget End
2003-01-31
Support Year
3
Fiscal Year
2002
Total Cost
$44,212
Indirect Cost
Name
Stanford University
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
800771545
City
Stanford
State
CA
Country
United States
Zip Code
94305
Alexander, David L; Arastu-Kapur, Shirin; Dubremetz, Jean-Francois et al. (2006) Plasmodium falciparum AMA1 binds a rhoptry neck protein homologous to TgRON4, a component of the moving junction in Toxoplasma gondii. Eukaryot Cell 5:1169-73
Bradley, Peter J; Ward, Chris; Cheng, Stephen J et al. (2005) Proteomic analysis of rhoptry organelles reveals many novel constituents for host-parasite interactions in Toxoplasma gondii. J Biol Chem 280:34245-58
Alexander, David L; Mital, Jeffrey; Ward, Gary E et al. (2005) Identification of the moving junction complex of Toxoplasma gondii: a collaboration between distinct secretory organelles. PLoS Pathog 1:e17