Skip to main content

Identification and Characterization of Biomarkers of Organophosphorus Exposures in Humans

  • Conference paper
  • First Online:
Book cover Paraoxonases in Inflammation, Infection, and Toxicology

Abstract

Over 1 billion pounds of organophosphorus (OP) chemicals are manufactured worldwide each year, including 70 million pounds of pesticides sprayed in the US. Current methods to monitor environmental and occupational exposures to OPs such as chlorpyrifos (CPS) have limitations, including low specificity and sensitivity, and short time windows for detection. Biomarkers for the OP tricresyl phosphate (TCP), which can contaminate bleed air from jet engines and cause an occupational exposure of commercial airline pilots, crewmembers and passengers, have not been identified.

The aim of our work has been to identify, purify, and characterize new biomarkers of OP exposure. Butyrylcholinesterase (BChE) inhibition has been a standard for monitoring OP exposure. By identifying and characterizing molecular biomarkers with longer half-lives, we should be able to clinically detect TCP and OP insecticide exposure after longer durations of time than are currently possible.

Acylpeptide hydrolase (APH) is a red blood cell (RBC) cytosolic serine proteinase that removes N-acetylated amino acids from peptides and cleaves oxidized proteins. Due to its properties, it is an excellent candidate for a biomarker of exposure. We have been able to purify APH and detect inhibition by both CPS and metabolites of TCP. The 120-day lifetime of the RBC offers a much longer window for detecting exposure. The OP-modified serine conjugate in the active site tryptic peptide has been characterized by mass spectrometry.

This research uses functional proteomics and enzyme activities to identify and characterize useful biomarkers of neurotoxic environmental and occupational OP exposures.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 169.00
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 219.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD 219.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

References

  • Aldridge WN (1954) Tricresyl phosphates and cholinesterase. Biochem J 56(2):185–189

    CAS  PubMed  Google Scholar 

  • Anderson L, Anderson NG (1977) High resolution two-dimensional electrophoresis of human plasma proteins. Proc Natl Acad Sci USA 74(12):5421–5425

    Article  CAS  PubMed  Google Scholar 

  • Black RM, Harrison JM, Read RW (1999) The interaction of sarin and soman with plasma proteins: the identification of a novel phosphonylation site. Arch Toxicol 73(2):123–126

    Article  CAS  PubMed  Google Scholar 

  • Casida JE, Eto M, Baron RL (1961) Biological activity of a tri-o-cresyl phosphate metabolite. Nature 191:1396–1397

    Article  CAS  PubMed  Google Scholar 

  • Casida JE, Quistad GB (2004) Organophosphate toxicology: safety aspects of nonacetylcholinesterase secondary targets. Chem Res Toxicol 17(8):983–998

    Article  CAS  PubMed  Google Scholar 

  • Fidder A, Hulst AG, Noort D, de Ruiter R, van der Schans MJ, Benschop HP, Lanenberg JP (2002) Retrospective detection of exposure to organophosphorus anti-cholinesterases: mass spectrometric analysis of phosphylated human butyrylcholinesterase. Chem Res Toxicol 15(4):582–590

    Article  CAS  PubMed  Google Scholar 

  • Fujino T, Watanabe K, Beppu M, Kikugawa K, Yasuda H (2000) Identification of oxidized protein hydrolase of human erythrocytes as acylpeptide hydrolase. Biochim Biophys Acta 1478(1):102–112

    CAS  PubMed  Google Scholar 

  • Furlong CE, Cole TB, MacCoss M, Richter R, Costa LG (2005) Biomarkers for Exposure and of Sensitivity to Organophosphorus [OP] Compounds. Proceedings of the BALPA Air Safety and Cabin Air Quality International Aero Industry Conference. April 20-21. Imperial College, London.

    Google Scholar 

  • Gade W, Brown JL (1978) Purification and partial characterization of alpha-N-acylpeptide hydrolase from bovine liver. J Biol Chem 253(14):5012–5018

    CAS  PubMed  Google Scholar 

  • Grunwald J, Marcus D, Papier Y, Raveh L, Pittel Z, Asani Y (1997) Large-scale purification and long-term stability of human butyrylcholinesterase: a potential bioscavenger drug. J Biochem Biophys Methods 34(2):123–135

    Article  CAS  PubMed  Google Scholar 

  • Hill RH, Head SL, Baker S, Gregg M, Shealy DB, Bailey SL, Williams CC, Sampson EJ, Needham LL (1995) Pesticide residues in urine of adults living in the United States: reference range concentrations. Environ Res 71(2):99–108

    Google Scholar 

  • Holmstedt B (1959) Pharmacology of organophosphorus cholinesterase inhibitors. Pharmacol Rev 11:567–688

    CAS  PubMed  Google Scholar 

  • Li B, Sedlacek M, Manoharan I, Boopathy R, Duysen EG, Masson P, Lockridge O (2005) Butyrylcholinesterase, paraoxonase, and albumin esterase, but not carboxylesterase, are present in human plasma. Biochem Pharmacol 70(11):1673–1684

    CAS  PubMed  Google Scholar 

  • Lockridge O, La Du B (1978) Comparison of atypical and usual human serum cholinesterase. Purification, number of active sites, substrate affinity, and turnover number. J Biol Chem 253(2):361–366

    CAS  PubMed  Google Scholar 

  • Lockridge O, Schopfer LM, Winger G, Woods JH (2005) Large scale purification of butyrylcholinesterase from human plasma suitable for injection into monkeys; a potential new therapeutic for protection against cocaine and nerve agent toxicity. J Med Chem Biol Radiol Def 3:5095

    Google Scholar 

  • Lotti M (1995) Cholinesterase inhibition: complexities in interpretation. Clin Chem 41:1814–1818

    CAS  PubMed  Google Scholar 

  • Mehrani H (2004) Simplified procedures for purification and stabilization of human plasma butyrylcholinesterase. Process Biochem 39(7):877–882

    Article  CAS  Google Scholar 

  • Parascandola J (1995) The Public Health Service and Jamaica ginger paralysis in the 1930 s. Public Health Reports 110(3):361–363

    CAS  PubMed  Google Scholar 

  • Peeples ES, Schopfer LM, Duysen EG, Spaulding R, Voelker T, Thompson CM, Lockridge O (2005) Albumin, a new biomarker of organophosphorus toxicant exposure, identified by mass spectrometry. Toxicol Sci 83(2):303–312

    Article  CAS  PubMed  Google Scholar 

  • Polhuijs M, Langenberg JP, Benschop HP (1997) New method for retrospective detection of exposure to organophosphorus anticholinesterases: application to alleged sarin victims of Japanese terrorists. Toxicol Appl Pharmacol 146(1):156–161

    Article  CAS  PubMed  Google Scholar 

  • Quistad GB, Klintenberg R, Casida JE (2005) Blood acylpeptide hydrolase activity is a sensitive marker for exposure to some organophosphate toxicants. Toxicol Sci 86(2):291–299

    Article  CAS  PubMed  Google Scholar 

  • Ralston JS, Main AR, Kilpathrick BF, Chasson AL (1983) Use of procainamide gels in the purification of human and horse serum cholinesterases. Biochem J 211(1):243–250

    CAS  PubMed  Google Scholar 

  • Richards PG, Johnson MK, Ray DE (2000) Identification of acylpeptide hydrolase as a sensitive site for reaction with organophosphorus compounds and a potential target for cognitive enhancing drugs. Mol Pharmacol 58(3):577–583

    CAS  PubMed  Google Scholar 

  • Saboori AM, Newcombe DS (1990) Human monocyte carboxylesterase. Purification and kinetics. J Biol Chem 265(32):19792–19799

    CAS  PubMed  Google Scholar 

  • Shimizu K, Kiuchi Y, Ando K, Hayakawa M, Kikugawa K (2004) Coordination of oxidized protein hydrolase and the proteasome in the clearance of cytotoxic denatured proteins. Biochem Biophys Res Commun 324(1):140–146

    Article  CAS  PubMed  Google Scholar 

  • Tsunasawa S, Narita K, Ogata K (1975) Purification and properties of acylamino acid-releasing enzyme from rat liver. J Biochem 77(1):89–102

    CAS  PubMed  Google Scholar 

  • Vose SC, Holland NT, Eskenazi B, Casida JE (2007) Lysophosphatidylcholine hydrolases of human erythrocytes, lymphocytes, and brain: sensitive targets of conserved specificity for organophosphorus delayed neurotoxicants. Toxicol Appl Pharmacol 224(1):98–104

    Article  CAS  PubMed  Google Scholar 

  • Whiteaker JR, Zhao L, Zhang HY, Feng LC, Piening BD, Anderson L, Paulovich AG (2007) Antibody-based enrichment of peptides on magnetic beads for mass-spectrometry-based quantification of serum biomarkers. Anal Biochem 362(1):44–54

    Article  CAS  PubMed  Google Scholar 

  • Winder C, Balouet JC (2002) The toxicity of commercial jet oils. Environ Res 89(2):146–164

    Article  CAS  PubMed  Google Scholar 

  • Yamaguchi M, Kambayashi D, Toda J, Sano T, Toyoshima S, Hojo H (1999) Acetylleucine chloromethyl ketone, an inhibitor of acylpeptide hydrolase, induces apoptosis of U937 cells. Biochem Biophys Res Commun 263(1):139–142

    Article  CAS  PubMed  Google Scholar 

  • Yamin R, Bagchi S, Hildebrant R, Scaloni A, Widom RL, Abraham CR (2007) Acyl peptide hydrolase, a serine proteinase isolated from conditioned medium of neuroblastoma cells, degrades the amyloid-beta peptide. J Neurochem 100(2):458–467

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgments

This work was supported by NIH Grants R01ES09883, P42ES04696, and NIEHS P30ES07033 (UW CEEH), as well as funding from Pilot Unions, Flight Attendant Unions, the Royal Australian Air Force, the Norwegian Union of Energy Workers (SAFE) and NYCO S.A. We thank Dr. Marian Ehrich for the kind gift of PSP, and Dr. Oksana Lockridge for BChE and anti-BChE antibodies.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Clement E. Furlong .

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2010 Humana Press, a part of Springer Science+Business Media, LLC

About this paper

Cite this paper

Kim, J.H. et al. (2010). Identification and Characterization of Biomarkers of Organophosphorus Exposures in Humans. In: Reddy, S. (eds) Paraoxonases in Inflammation, Infection, and Toxicology. Advances in Experimental Medicine and Biology, vol 660. Humana Press. https://doi.org/10.1007/978-1-60761-350-3_7

Download citation

Publish with us

Policies and ethics