Indirect ELISA Method for Measurement of Lactoperoxidase using IgY Antibody

IgY 항체를 이용하여 Lactoperoxidase 정량을 측정하기 위한 Indirect ELISA 방법의 개발

  • Published : 2004.06.01

Abstract

To determine the concentration of Lactoperoxidase (LPO), an indirect enzyme-linked immunosorbant assay(ELISA) was developed. Anti-LPO egg yolk immunoglobulin(IgY) was transferred to egg yolk by immunizing of Brown hens with LPO. The titer of purified anti-LPO IgY was 1: 520,000. The immunological response of anti- LPO IgY with ${\alpha}$-lactalbumin, ${\beta}$-lactoglobulin, casein and lysozyme were evaluated, resulting that the anti-LPO IgY found to be a specific antibody toward LPO and no cross-reaction was observed against ${\alpha}$-lactalbumin, ${\beta}$-lactoglobulin, casein, and lysozyme in double immunodiffusion test and ELISA test. In indirect ELISA method, coating concentration of LPO and dilution rate of anti-LPO IgY was 0.25$\mu\textrm{g}$/mL and 1:8,000 respectively. Sensitivity in the standard curve of LPO was ranged from 0.01 to 1$\mu\textrm{g}$/mL using anti-LPO IgY.

Lactoperoxidase(LPO)를 농도를 측정하기 위한 ELISA을 개발하기 위해 LPO로 면역시킨 갈색 산란계의 계란에서 형성된 anti-LPO IgY 항체를 분리 정제하고, 분리된 anti-LPO IgY 항체의 특이성을 ELISA 와 double immunodiffusion 방법으로 조사한 후 indirect ELISA 방법을 이용한 표준곡선을 만들었다. 분리 정제된 anti-LPO IgY항체의 titer는 1:520,000이며, ELISA와 double immunodiffusion 방법 모두에서 $\alpha$-lactalbumin, $\beta$-lactoglobulin, casein 및 lysozyme하고는 교차반응을 하지 않고 LPO만 높은 특이성을 갖는 항체로 나타났다. Indirect ELISA방법에서 LPO의 coating 농도는 0.25 $\mu\textrm{g}$/mL이며 anti-LPO IgY 최적 희석배수는 1:8,000으로 나타났다. Indirect ELISA 방법으로 LPO를 측정할 수 있는 표준곡선에서 민감도의 범위는 0.0l-l $\mu\textrm{g}$/mL로 나타났다.

Keywords

References

  1. Akita, E. M. and Nakai, S. (1992) Immunoglobulin from egg yolk; isolation and purification. J. Food Sci. 57, 629-634 https://doi.org/10.1111/j.1365-2621.1992.tb08058.x
  2. Andrews, A. T., Anderson, M, and Goodnough, P. W. (1987) A study of heat stabilities of number of indigenous milk enzymes. J. Dairy Res. 54, 237-246 https://doi.org/10.1017/S0022029900025371
  3. Bjorck, L., Rosen, C., Marshall, V., and Reiter, B. (1975) Antibacterial activity of the lactoperoxidase system in milk against Pseudomonas and other gram negative bacteria. Appl. Microbiol. 30, 199-204
  4. De Ceuninck, F., Pastoureau, P., agnellet, S., Bonnet, J. and Vanhoutte, P. M. (2001) Development of an enzyme-linked immunoassay for the quantification of YKL-40(cartilage gp-39) in guinea pig serum using hen egg yolk antibodies. J. Immunol. Methods 252, 153-161 https://doi.org/10.1016/S0022-1759(01)00352-0
  5. Clarke, J. R., Marquardt, R. R., Frohlich, A. A. and Pitura, R. J. (1994) Quantification of ochratoxin A in swine kid-neys by enzyme-linked immunosorbent assay using a simp-lified sample preparation procedure. J. Food Protect. 57, 991-995
  6. De wit, J. N. and van Hooydonk, A. C. M. (1966) Structure, function and applications of lactoperoxidase in natural antimicrobial systems. Neth. Milk Dairy J. 50, 227-244
  7. Earnshaw, R. G., Banks, J. G., Derise, D., and Francotte, C. (1989) The preservation of cottage cheese by an activated lactoperoxidase system. Food Microbiol. 6. 285-288 https://doi.org/10.1016/S0740-0020(89)80010-3
  8. Farkey, N. Y. and Imafidon, G. I. (1995) Thennal dena-turation of indigenous milk enzyme. In Heat Induced Change in Milk, 2nd ed., International Dairy, Federation, Brussels, I. 9501, pp. 331-348
  9. Frazier, W. C. (1988) Preservation by drying In Food Microbiology, Frazier, W. C.(ed), McGraw-Hill, NY, USA, pp. 125-131
  10. Gassmann, M., Thommes, P., Weiser, T., and Hubscher, U. (1990) Efficient production of chicken egg yolk antibodies against a conserved mammalian protein. FASEB J. 4, 2528-2532
  11. Griffiths, M. W. (1986) Use of milk enzymes as indices of heat treatment. J. Food Prot. 49, 696-705
  12. Jenness, R. (1982) Inter-species comparison of milk protein. In Developments in dairy chemistry-I, Fox, P. F.(ed) App. Sci. Pub. London, England, pp.87-114
  13. Karnau, D. N., Doores, S., and Pruitt, K. M. (1990) Enhanced thermal destruction of Listeria monocytogenes and Staphylococcus aureus by the lactoperoxidase system. Appl. Environ. Microbiol. 56, 2711-2716
  14. Kennedy, M., O'rourke, A. L., Mclay, J., and Simmonds, R. (2000) Use of ground beef model to assess the effect of the lactoperoxidase system on the growth of Escherichia coli O157:H7, Listeria monocytogenes and Staphylococcus aureus in red meat. Inter. J. Food Microbiol. 57, 147-158 https://doi.org/10.1016/S0168-1605(99)00208-1
  15. Kim, C. H., Lee, K. W., Baick, S. C., and Moon, J. W. (1996) Inhibition of acid production in gel type yogurt by the lactoperoxidase system. Korean J. Food Technol. 28, 736-742
  16. Knekt, P., Jarvinen, R., Dich, J., and Hakulinen, T. (1999) Risk of colorectal and other gastro-intestinal cancers after exposure to nitrate, nitrite and N-nitroso compounds: a follow-up study. Int. J Cancer 80, 852-856 https://doi.org/10.1002/(SICI)1097-0215(19990315)80:6<852::AID-IJC9>3.0.CO;2-S
  17. Larsson, A., Balow, R., Lindahl, T. L., and Forsberg, P. (1993) Chicken antibodies: taking advantage of evolution -a review. Poult. Sci. 72, 1807-1812 https://doi.org/10.3382/ps.0721807
  18. Lee, S. B., Choi, S. H., and Baek D. Y. (1999) Immunogical characteristics of anti-lactoferrin IgY and immunoassay of lactoferrin in milk. Korean J. Dairy Sci. 21, 299-304
  19. Lee, S. B., Mine, Y., and Stevenson R. M. W. (2000) Effects of hen egg yolk immunoglobulin in passive protection of rainbow trout against Yersinia ruckeri. J. Agri. Food Chem. 48, 110-115 https://doi.org/10.1021/jf9906073
  20. Nakada, M., Dosako, S., Hirano, R., Ooka, M., and Naka-jima, I. (1966) Lactoperoxidase suppresses acid production in yoghurt during storage under refrigeration, Int. Dairy J. 6, 33-42 https://doi.org/10.1016/0958-6946(94)00053-0
  21. Ouchterlony, O. and Nilsson, L. A. (1978) Immunodiffusion and immunoelectrophoresis. In Handbook of Experimental Immunology, 3rd. ed., Weir D.M.(ed.), Chapter 19. Blackwell Sci. Publ., Oxford
  22. Pellegrino, L., Resmini, P., and Luf, W. (1995) Asse-ssment( indices) of heat treatments of milk, In Heat Induced Change in Milk, International Dairy, Federation S. I. 9501(2nd ed.), Brussels, pp. 695-705
  23. Reiter, B. (1985) The lactoperoxidase system of bovine milk. In The lactoperoxidase System, Chemistry and Biological Significance, Pruitt, K. M. and Tenovuo, J. O. (eds), Marcel Dekker, NY, pp. 123-142
  24. Sauer, M. J. and Foulkes, J. A. (1985) Principles of enzyme immunoassay. In Immunoassay in Food Analysis, Morris, B. A. and Clifford, M. N.(eds). Elsevier Applied Sci. Publ., London and NY, pp. 53-72
  25. Shin, K, Hayasawa, H., and Lonnerdal, B. (2001) Purifi-cation and quantification of lactoperoxidase in human milk with use of immunoadsorbents with antibodies against recombinant human lactoperoxidase. Am. J. Clin. Nutr. 73, 984-989
  26. Tenovuo, J. O. (1985) The peroxidase system in human secretions. In The lactoperoxidase System, Chemistry. and Biological Significance. Pruitt, K. M. and Tenovuo, J. o.(eds), Marcel Dekker, NY, pp. 101-122
  27. Wolfson, L. M, Sumner, S. S., and Froning, G. W. (1994) Inhibition of Salmonella thphimurium on poultry by the lactoperoxidase system. J. Food Saf. 14, 53-62 https://doi.org/10.1111/j.1745-4565.1994.tb00583.x