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Direct Detection and Quantitative Determination of Bovine Lactoferricin and Lactoferrin Fragments in Human Gastric Contents by Affinity Mass Spectrometry

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Part of the book series: Advances in Experimental Medicine and Biology ((AEMB,volume 443))

Abstract

Lactoferricin (Lfcin®) is a bioactive fragment of lactoferrin derived from the bactericidal and putative lymphocyte receptor binding domain(s) located within the N-lobe of lactoferrin. Although known to be liberated from at least three species of lactoferrin, conditions leading to Lfcin generation in vivo and factors affecting its distribution are still not known. Recently, we have developed a method of surface-enhanced laser desorption/ionization (SELDI®) affinity mass spectrometry using n-butyl terminal groups for surface-enhanced affinity capture (SEAC) to quantify not only Lfcin generated in vivo but also other lactoferrin fragments. Unlike previous efforts to detect lactoferrin and Lfcin with specific antibodies, the SELDI affinity assay distinguished lactoferrin, lactoferrin fragments, Lfcin and unrelated peptides without their interference with each other. To evaluate Lfcin generation in vivo, the experimental design involved feeding 200 mL of 10 mg/mL (1.22 × 10−4 mol/L) bovine lactoferrin to an adult. Gastric contents were recovered 10 min after ingestion. Lfcin produced in vivo was directly captured by the SEAC device. The amount of Lfcin in the gastric contents was 16.91 ± 2.65 sg/mL (5.350 ± 0.838 × 10−6 mol/L). However, a large proportion of the ingested lactoferrin was not completely digested. Lactoferrin fragments containing the Lfcin region were analyzed by in situ hydrolysis with pepsin after being captured by the SEAC device. As much as 5.740 ± 0.702 x 10−5 mol/L of the partially degraded lactoferrin fragments were found to contain the Lfcin region, including peptide domains 17–43, 17–44, 12–44, 9–58, and 16–76 of bovine lactoferrin. These results show that bovine Lfcin can be produced in the human stomach after ingestion of an infant formula supplemented with bovine lactoferrin. It is now important to determine whether Lfcin is generated in the intestinal tract of formula-fed and breast-fed infants, and geriatric patients consuming foods enriched with lactoferrin.

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References

  1. Masson, P. L., Heremans, J. E, and Dive, J. H. (1966) An iron-binding protein common to many external secretions. Clin.Chim. Acta 14, 735–739.

    CAS  Google Scholar 

  2. Masson, P. L., Heremans, J. F., and Schonne, E. (1969) Lactoferrin, an iron-binding protein in neutrophilic leukocytes. J. Exp. Med. 130, 643–658.

    Article  PubMed  CAS  Google Scholar 

  3. Bennett, R. M., Eddie-Quartey, A. C., and Holt, P. J. L. (1973) Lactoferrin—an iron binding protein in synovial fluid. Arthritis and Rheumatism 16, 186–190.

    Article  PubMed  CAS  Google Scholar 

  4. Sanchez, L., Calvo, M.. and Brock, J. H. (1992) Biological role of lactoferrin. Arch. Dis. Child 67, 657–661.

    Article  PubMed  CAS  Google Scholar 

  5. Bellamy, W., Takase, M., Yamauchi, K., Wakabayashi, H., Kawase, K., and Tornita, M. (1992) Identification of the bactericidal domain of lactoferrin. Biochim. Biophys. Acta 1121, 130–136.

    Google Scholar 

  6. Legrand, D., Mazurier, J.. Elass, A., Rochard, E., Vergoten, G., Maes, P., Montreuil, J., and Spik, G. (1992) Molecular interactions between human lactotransferrin and the phytohemagglutinin-activated human lymphocyte lactotransferrin receptor lie in two loop-containing regions of the N-terminal domain of human lactotransferrin. Biochemistry 3l, 9243–9251.

    Article  Google Scholar 

  7. Mann, D. M., Romm, E., and Migliorini, M. (1994) Delineation of the glycosaminoglycan-binding site in the human inflammatory response protein lactoferrin. J. Biol. Chem. 269, 23661–23667.

    PubMed  CAS  Google Scholar 

  8. Elass-Rochard, E., Roseanu, A., Legrand, D., Trif, M., Salmon, V., Motas, C., Montreuil, J., and Spik, G. (1995) Lactoferrin-lipopolysaccharide interaction: involvement of the 28–34 loop region of human lactoferrin in the high-affinity binding to Escherichia coli O55B5 lipopolysaccharide. Biochem. J. 312, 839–845.

    PubMed  CAS  Google Scholar 

  9. Roberts, A. K., Chierici, R., Sawatzki, G., Hill, M.. 1., Volpato, S., and Vigi, V. (1992) Supplementation of an adapted formula with bovine lactoferrin: 1. Effect on the infant faecal flora. Acta Paediatr. 81, 1 19–124.

    Google Scholar 

  10. Teraguchi, S., Ozawa, K., Yasuda, S., Shin, K., Fukuwatari, Y., and Shimamura, S. (1994) The bacteriostatic effects of orally administered bovine lactoferrin on intestinal Enterobacteriaceae of SPF mice fed bovine milk. Biosci., Biotechnol., Biochem. 58, 482–487.

    CAS  Google Scholar 

  11. Hentges, D. J., Marsh, W. W., Petschow, B. W., Thal, W. R., and Carter, M. K. (1992) Influence of infant diets on the ecology of the intestinal tract of human flora-associated mice. J. Pediatr. Gastroenterol Nutr. 14, 146–152.

    Article  PubMed  CAS  Google Scholar 

  12. Spik, G., Brunet, B.. Mazurier-Dehaine, C., Fontaine, G., and Montreuil, J. (1982) Characterization and properties of the human and bovine lactotransferrins extracted from the faeces of newborn infants. Acta Paediatr. Scand. 71, 979–985.

    CAS  Google Scholar 

  13. Hutchens, T. W., Henry, J. F., Yip, T. T., Hachey, D. L., Schanler, R. J., Motil, K. J., and Garza, C. (1991) Origin of intact lactoferrin and its DNA-binding fragments found in the urine of human milk-fed preterm infants. Evaluation by stable isotopic enrichment. Pediatr. Res. 29, 243–250.

    Article  PubMed  CAS  Google Scholar 

  14. Duncan, M. W., Matanovic, G., and Cerpa-Poljak, A. (1993) Quantitative analysis of low molecular weight compounds of biological interest by matrix-assisted laser desorption ionization. Rapid Commun. Mass Spectrom. 7, 1090–1094.

    CAS  Google Scholar 

  15. Gusev, A. 1., Wilkinson, W. R., Proctor, A., and Hercules, D. M. (1993) Quantitative analysis of peptides by matrix-assisted laser desorption ionization time-of-flight mass spectrometry. Appl. Spectrosc. 47, 1091–1092.

    CAS  Google Scholar 

  16. Nelson, R. W., Mclean, M. A., and Hutchens, T. W. (1994) Quantitative determination of proteins by matrix-assisted laser desorption ionization time-of-flight mass spectrometry. Anal. Chem. 66, 1408–1415.

    Article  CAS  Google Scholar 

  17. Hutchens, T. W. and Yip, T. T. (1993) New desorption strategies for the mass spectrometric analysis of macromolecules. Rapid Commun. Mass Spectrum. 7, 576–580.

    CAS  Google Scholar 

  18. Yip, T. T., Van deWater, J., Gershwin, M. E., Coppel, R. L., and Hutchens, T. W. (1996) Cryptic antigenic determinants on the extracellular pyruvate dehydrogenase complex/mimeotope found in primary biliary cirrhosis. A probe by affinity mass spectrometry. J. Biol. Chem. 271, 32825–32833.

    Article  PubMed  CAS  Google Scholar 

  19. Kuwata, H., Yip, T. T., Yip, C. L., and Hutchens, T. W. Bactericidal domain of lactoferrin. Detection, quantitation, and characterization of lactoferricin in serum by SELDI affinity mass spectrometry. Manuscript in preparation

    Google Scholar 

  20. Hutchens, T. W., Nelson, R. W., Allen, M. H., Li, C. M., and Yip, T. T. (1992) Peptide-metal ion interactions in solution:detection by laser desorption time-of-flight mass spectrometry and electrospray ionization mass spectrometry. Biol. Mass Spectrom. 21, 151–159.

    Article  CAS  Google Scholar 

  21. Bellamy, W., Takase, M., Wakabayashi, H., Kawase, K., and Tornita, M. (1992) Antibacterial spectrum of lactoferricin B, a potent bactericidal peptide derived from the N-terminal region of bovine lactoferrin. J. Appl. Bacteriol. 73, 472–479.

    Article  PubMed  CAS  Google Scholar 

  22. Yoshioka, H., Iseki, K., and Fujita, K. (1983) Development and differences of intestinal flora in the neonatal period in breast-fed and bottle-fed infants. Pediatrics 27, 317–320.

    Google Scholar 

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Kuwata, H., Yip, TT., Yip, C.L., Tomita, M., Hutchens, T.W. (1998). Direct Detection and Quantitative Determination of Bovine Lactoferricin and Lactoferrin Fragments in Human Gastric Contents by Affinity Mass Spectrometry. In: Spik, G., Legrand, D., Mazurier, J., Pierce, A., Perraudin, JP. (eds) Advances in Lactoferrin Research. Advances in Experimental Medicine and Biology, vol 443. Springer, Boston, MA. https://doi.org/10.1007/978-1-4757-9068-9_3

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  • DOI: https://doi.org/10.1007/978-1-4757-9068-9_3

  • Publisher Name: Springer, Boston, MA

  • Print ISBN: 978-1-4757-9070-2

  • Online ISBN: 978-1-4757-9068-9

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