This subproject is one of many research subprojects utilizing theresources provided by a Center grant funded by NIH/NCRR. The subproject andinvestigator (PI) may have received primary funding from another NIH source,and thus could be represented in other CRISP entries. The institution listed isfor the Center, which is not necessarily the institution for the investigator.The most significant risk factor for neurodegeneration is aging. Strong evidence implicates protein aggregation-mediated toxicity as the cause of neurodegeneration in numerous clinically important diseases, although the mechanism(s) remains unclear. Alzheimer's disease is thought to be caused by the proteotoxicity resulting from misassembly of the secreted amyloid-beta family of peptides, the longest of which are the most aggregation prone and closely linked to pathology. In this project we strive to understand the molecular basis for protection from proteotoxicity using quantitative proteomics.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biotechnology Resource Grants (P41)
Project #
5P41RR011823-13
Application #
7723613
Study Section
Special Emphasis Panel (ZRG1-CB-H (40))
Project Start
2008-09-01
Project End
2009-08-31
Budget Start
2008-09-01
Budget End
2009-08-31
Support Year
13
Fiscal Year
2008
Total Cost
$819
Indirect Cost
Name
University of Washington
Department
Biochemistry
Type
Schools of Medicine
DUNS #
605799469
City
Seattle
State
WA
Country
United States
Zip Code
98195
Xavier, Marina Amaral; Tirloni, Lucas; Pinto, Antônio F M et al. (2018) A proteomic insight into vitellogenesis during tick ovary maturation. Sci Rep 8:4698
Hollmann, Taylor; Kim, Tae Kwon; Tirloni, Lucas et al. (2018) Identification and characterization of proteins in the Amblyomma americanum tick cement cone. Int J Parasitol 48:211-224
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