The long range objective of this project is to elucidate the mechanisms by which the physiological action of opioid peptides is terminated. The research will focus on the role of two peptidases, a neutral endopeptidase and an enkephalin degrading aminopeptidase, as """"""""enkephalinases"""""""". The neutral endopeptidase has been shown to exist in multiple forms in kidney and brain. A cDNA clone to the neutral endopeptidase will be isolated. The cDNA will be used to probe brain mRNA for the existence of multiple messages for the enzyme. In addition, the cDNA will be used to determine the amino acid sequence of the enzyme. In conjunction with these studies, the nature of the multiple forms of the enzyme will be investigated by biochemical techniques with particular emphasis on the carbohydrate structure of the enzyme. Studies will also be conducted of the effects of non-opioid peptides on the degradation of opioid peptides. These studies will focus on the ability of non-opioid peptides to inhibit the neutral endopeptidase and the enkephalin degrading aminopeptidase. The latter enzyme will be characterized in terms of its localization in brain and its relationship to other aminopeptidases. Lastly, the pathways for degradation of the dynorphins will be studied in crude brain membrane fractions. The degradative pathways will be established, and the peptidases involved will be partially purified and characterized.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Research Project (R01)
Project #
5R01DA002243-12
Application #
3207201
Study Section
(DABB)
Project Start
1978-09-30
Project End
1991-02-28
Budget Start
1989-03-01
Budget End
1990-02-28
Support Year
12
Fiscal Year
1989
Total Cost
Indirect Cost
Name
University of Texas Sw Medical Center Dallas
Department
Type
Overall Medical
DUNS #
City
Dallas
State
TX
Country
United States
Zip Code
75390
Song, Eun Suk; Ozbil, Mehmet; Zhang, Tingting et al. (2015) An Extended Polyanion Activation Surface in Insulin Degrading Enzyme. PLoS One 10:e0133114
Guan, Hanjun; Chow, K Martin; Song, Eunsuk et al. (2015) The Mitochondrial Peptidase Pitrilysin Degrades Islet Amyloid Polypeptide in Beta-Cells. PLoS One 10:e0133263
Sexton, Travis; Hitchcook, Lisa J; Rodgers, David W et al. (2012) Active site mutations change the cleavage specificity of neprilysin. PLoS One 7:e32343
Guan, H; Chow, K M; Shah, R et al. (2012) Degradation of islet amyloid polypeptide by neprilysin. Diabetologia 55:2989-98
Noinaj, Nicholas; Song, Eun Suk; Bhasin, Sonia et al. (2012) Anion activation site of insulin-degrading enzyme. J Biol Chem 287:48-57
Song, Eun Suk; Melikishvili, Manana; Fried, Michael G et al. (2012) Cysteine 904 is required for maximal insulin degrading enzyme activity and polyanion activation. PLoS One 7:e46790
Song, Eun Suk; Rodgers, David W; Hersh, Louis B (2011) Mixed dimers of insulin-degrading enzyme reveal a cis activation mechanism. J Biol Chem 286:13852-8
Chirra, Hariharasudhan D; Sexton, Travis; Biswal, Dipti et al. (2011) Catalase-coupled gold nanoparticles: comparison between the carbodiimide and biotin-streptavidin methods. Acta Biomater 7:2865-72
Noinaj, Nicholas; Bhasin, Sonia K; Song, Eun Suk et al. (2011) Identification of the allosteric regulatory site of insulysin. PLoS One 6:e20864
Shen, Xin-Ming; Crawford, Thomas O; Brengman, Joan et al. (2011) Functional consequences and structural interpretation of mutations of human choline acetyltransferase. Hum Mutat 32:1259-67

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