? During the proposed renewal period, we will extend advances made in the preceding five years. These involve a number of areas. Proposals described in detail in the Research Design section include elucidating further our discovery that IP7 physiologically phosphorylates a variety of proteins in diverse species. We will also continue our studies establishing IP6 kinase-2 as a physiologic mediator of cell death. We will clarify our observations that the enzyme we first discovered as inositol polyphosphate multikinase (IPMK) also is a major nuclear PI3-kinase. Additionally, we will move forward working out a novel cell death cascade whereby apoptotic stimuli activate inducible NO synthase to generate NO that S-nitrosylates glyceraldehyde- 3-phosphate dehydrogenase (GAPDH) enabling it to bind Siah, translocate to the nucleus and cause cell death by enhancing the turnover of as yet unspecified proteins. ? ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Research Scientist Award (K05)
Project #
5K05DA000074-28
Application #
7281237
Study Section
Human Development Research Subcommittee (NIDA)
Program Officer
Pollock, Jonathan D
Project Start
1980-07-01
Project End
2010-08-31
Budget Start
2007-09-01
Budget End
2008-08-31
Support Year
28
Fiscal Year
2007
Total Cost
$129,276
Indirect Cost
Name
Johns Hopkins University
Department
Neurosciences
Type
Schools of Medicine
DUNS #
001910777
City
Baltimore
State
MD
Country
United States
Zip Code
21218
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