Serine hydrolase targets of organophosphorus toxicants

Chemico-Biological Interactions

Volumn 157-158, Issue , 2005, Pages 277-283

  Casida, John E ^a   Quistad, Gary B ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

Acetylcholinesterase; Chemical warfare agent; Insecticide; Neurotransmitter receptor; Organophosphorus; Serine hydrolase

Indexed keywords

1 ALKYL 2 ACETYLGLYCEROPHOSPHOCHOLINE ESTERASE; ARYLFORMAMIDASE; CANNABINOID 1 RECEPTOR; CARBOXYLESTERASE; CHLORPYRIFOS; CHOLINESTERASE; ECOTHIOPATE; LYSOPHOSPHOLIPASE; METRIFONATE; ORGANOPHOSPHATE PESTICIDE; PESTICIDE; SERINE DEHYDRATASE;

ALZHEIMER DISEASE; ANTHELMINTIC ACTIVITY; CHEMICAL PEST CONTROL; CONFERENCE PAPER; EGG; ENVIRONMENTAL EXPOSURE; GLAUCOMA; HEN; HUMAN; HYDROLYSIS; NEUROPATHY; NONHUMAN; OCCUPATIONAL EXPOSURE; RISK ASSESSMENT; SCHISTOSOMA; WORM INFECTION;

ANIMALS; HUMANS; ORGANOPHOSPHORUS COMPOUNDS; SERINE ENDOPEPTIDASES; SERINE PROTEINASE INHIBITORS; STRUCTURE-ACTIVITY RELATIONSHIP;

SCHISTOSOMA; VERTEBRATA;

EID: 28744452920     PISSN: 00092797     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cbi.2005.10.036     Document Type: Conference Paper

References (29)

1. M.J. O'Neil The Merck Index 13th ed. 2001 Merck & Co. Inc. Whitehouse Station, NJ
2. C.D.S. Tomlin The Pesticide Manual 13th ed. 2003 British Crop Protection Council Hampshire, UK pp. 1344
3. E. Giacobini Cholinesterases and Cholinesterase Inhibitors 2000 Martin Dunitz Ltd. London, UK pp. 270
4. J.E. Casida, and G.B. Quistad Organophosphate toxicology: safety aspects of nonacetylcholinesterase secondary targets Chem. Res. Toxicol. 17 2004 983 998
5. International Human Genome Sequencing Consortium, Finishing the euchromatic sequence of the human genome, Nature 431 (2004) 931-945.
6. G.M. Rubin and 54 other authors Comparative genomics of the eukaryotes Science 287 2000 2204 2215
7. J.C. Venter and >100 other authors The sequence of the human genome Science 291 2001 1304 1351
8. G.M. Yousef, A.D. Kopolovic, M.B. Elliott, and E.P. Diamandis Genomic overview of serine proteases Biochem. Biophys. Res. Commun. 305 2003 28 36
9. W.N. Aldridge, and E. Reiner Enzyme Inhibitors as Substrates: Interactions of Esterases with Esters of Organophosphorus and Carbamic Acids 1972 North-Holland Publishing Amsterdam pp. 328
10. Y. Liu, M.P. Patricelli, and B.F. Cravatt Activity-based protein profiling: the serine hydrolases Proc. Natl. Acad. Sci. USA 96 1999 14694 14699
11. D. Kidd, Y. Liu, and B.F. Cravatt Profiling serine hydrolase activities in complex proteomes Biochemistry 40 2001 4005 4015
12. N. Jessani, Y. Liu, M. Humphrey, and B.F. Cravatt Enzyme activity profiles of the secreted and membrane proteome that depict cancer cell invasiveness Proc. Natl. Acad. Sci. U.S.A. 99 2002 10335 10340
13. D. Leung, C. Hardouin, D.L. Boger, and B.F. Cravatt Discovering potent and selective reversible inhibitors of enzymes in complex proteomes Nat. Biotechnol. 21 2003 687 691
14. N. Jessani, M. Humphrey, W.H. McDonald, S. Niessen, K. Masuda, B. Gangadharan, J.R. Yates III, B.M. Mueller, and B.F. Cravatt Carcinoma and stromal enzyme activity profiles associated with breast tumor growth in vivo Proc. Natl. Acad. Sci. U.S.A. 101 2004 13756 13761
15. L.L. Jennings, M. Malecki, E.A. Komives, and P. Taylor Direct analysis of the kinetic profiles of organophosphate-acetylcholinesterase adducts by MALDI-TOF mass spectrometry Biochemistry 42 2003 11083 11091
16. 3H]benzodioxaphosphorin 2-oxide J. Neurochem. 64 1995 1680 1687
17. E.S. Peeples, L.M. Schopfer, E.G. Duysen, R. Spaulding, T. Voelker, C.M. Thompson, and O. Lockridge Albumin, a new biomarker of organophosphorus toxicant exposure, identified by mass spectrometry Toxicol. Sci. 83 2005 303 312
18. H. Li, L. Schopfer, R. Spaulding, C.M. Thompson, O. Lockridge, Identification of organophosphate-reactive proteins by tandem mass spectrometry, Poster Presentation in the VIIIth International Meeting on Cholinesterases, Perugia, Italy, 26-30 September 2004.
19. G.B. Quistad, K.J. Fisher, S.C. Owen, R. Klintenberg, and J.E. Casida Platelet-activating factor acetylhydrolase: selective inhibition by potent n-alkyl methylphosphonofluoridates Toxicol. Appl. Pharmacol. 205 2005 149 156
20. G.B. Quistad, R. Klintenberg, and J.E. Casida Blood acylpeptide hydrolase activity is a sensitive marker for exposure to some organophosphate toxicants Toxicol. Sci. 86 2005 291 299
21. K. Akassoglou, B. Malester, J. Xu, L. Tessarollo, J. Rosenbluth, and M.V. Chao Brain-specific deletion of neuropathy target esterase/swisscheese results in neurodegeneration Proc. Natl. Acad. Sci. U.S.A. 101 2004 5075 5080
22. H. Koizumi, N. Yamaguchi, M. Hattori, T. Ishikawa, J. Aoki, M.M. Taketo, K. Inoue, and H. Arai Targeted disruption of intracellular type I platelet activating factor-acetylhydrolase catalytic subunits causes severe impairment in spermatogenesis J. Biol. Chem. 278 2003 12489 12494
23. Δex4 mutation replicate the INCL phenotype and show an inflammation-associated loss of interneurons Neurobiol. Disease 18 2005 226 241
24. V.N. Dobrovolsky, J.F. Bowyer, M.K. Pabarcus, R.H. Heflich, L.D. Williams, D.R. Doerge, B. Arvidsson, J. Bergquist, and J.E. Casida Effect of arylformamidase (kynurenine formamidase) gene inactivation in mice on enzymatic activity, kynurenine pathway metabolites and phenotype Biochim. Biophys. Acta 1724 2005 163 172
25. O. Lockridge, R.M. Blong, P. Masson, M.-T. Froment, C.B. Millard, and C.A. Broomfield A single amino acid substitution, Gly117His, confers phosphotriesterase (organophosphorus acid anhydride hydrolase) activity on human butyrylcholinesterase Biochemistry 36 1997 786 795
26. L.G. Costa C.E. Furlong Paraoxonase (PON1) in Health and Disease 2002 Kluwer Academic Publishers Norwell, MA pp. 216
27. Y. Kondo, A. Ishigami, S. Kubo, S. Handa, K. Gomi, K. Hirokawa, N. Kajiyama, T. Chiba, K. Shimokado, and N. Maruyama Senescence marker protein-30 is a unique enzyme that hydrolyzes diisopropyl phosphorofluoridate in the liver Fed. Eur. Biochem. Soc. Lett. 570 2004 57 62
28. I. Yamamoto, N. Kyomura, and Y. Takahashi Negatively correlated cross resistance: combinations of N-methylcarbamate with N-propylcarbamate or oxadiazolone for green rice leafhopper Arch. Insect. Biochem. Physiol. 22 1993 277 288
29. Isaiah 2:4.