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Two Efficient Methods for the Conjugation of Smooth-Form Lipopolysaccharides with Probes Bearing Hydrazine or Amino Groups. I. LPS Activation with Cyanogen Bromide

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Microbial Toxins

Part of the book series: Methods in Molecular Biology ((MIMB,volume 739))

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Abstract

This chapter presents a conjugation method for coupling probes bearing hydrazine or primary amino groups to a smooth(S)-form lipopolysaccharide (LPS). LPS is modified by the activation of the hydroxyl groups present in its O-antigen moiety with cyanogen bromide in aqueous acetone. The method yields conjugates with good labeling ratios, preserving the endotoxic activity of the lipid A moiety. Conjugation of smooth-form LPS from Salmonella enterica sv. Minnesota with dansyl hydrazine and horseradish ­peroxidase yields labeling ratios above 300 nmol dansyl per mg LPS, with nearly no loss of the original endotoxin activity. In the case of horseradish peroxidase, introducing a spacer, a ratio of 28 nmol HRP per mg LPS is obtained, preserving 65% of the original endotoxic activity.

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References

  1. Morrison DC, Ryan JL (eds) (1992) Bacterial endotoxic lipopolysaccharides. Vol I. Molecular biochemistry and cellular biology. CRC, Boca Raton

    Google Scholar 

  2. Troelstra A, Antal-Szalmas P, De Graaf-Miltenburg LAM, Weersink AJL, Verhoef J, VanKessel KPM, VanStrijp JAG (1997) Saturable CD14-dependent binding of fluorescein-labeled lipopolysaccharide to human monocytes. Infect Immun 65:2272–2277

    PubMed  CAS  Google Scholar 

  3. Tobias PS, Soldau K, Gegner JA, Mintz D, Ulevitch RJ (1995) Lipopolysaccharide-binding protein-mediated complexation of lipopolysaccharide with soluble CD14. J Biol Chem 270:10482–10488

    Article  PubMed  CAS  Google Scholar 

  4. Luk JM, Kumar A, Tsang R, Staunton D (1995) Biotinylated lipopolysaccharide binds to endotoxin receptor in endothelial and monocytic cells. Anal Biochem 232:217–224

    Article  PubMed  CAS  Google Scholar 

  5. Priano G, Pallarola D, Battaglini F (2007) Endotoxin detection in a competitive electrochemical assay: synthesis of a suitable endotoxin conjugate. Anal Biochem 362:108–116

    Article  PubMed  CAS  Google Scholar 

  6. Kohn J, Wilchek M (1982) A new approach (cyano-transfer) for cyanogen-bromide activation of sepharose at neutral pH, which yields activated resins, free of interfering nitrogen derivatives. Biochem Biophys Res Commun 107:878–884

    Article  PubMed  CAS  Google Scholar 

  7. Wilchek M, Miron T, Kohn J (1984) Affinity chromatography. Methods Enzymol 104:3–55

    Article  PubMed  CAS  Google Scholar 

  8. Pallarola D, Battaglini F (2008) An efficient method for conjugation of a lipopolysaccharide from Salmonella enterica sv. Minnesota with probes bearing hydrazine or amino functional groups. Anal Biochem 381:53–58

    Article  PubMed  CAS  Google Scholar 

  9. Bergethon P (1998) The physical basis of biochemistry. Springer, New York, pp 254–256

    Google Scholar 

  10. Lee CH, Tsai CM (1999) Quantification of bacterial lipopolysaccharides by the purpald assay: measuring formaldehyde generated from 2-keto-3-deoxyoctonate and heptose at the inner core by periodate oxidation. Anal Biochem 267:161–168

    Article  PubMed  CAS  Google Scholar 

  11. Chance B, Maehly ACE (1955) Preparation and assays of enzymes. Methods Enzymol 2:773–775

    Google Scholar 

  12. Hirayama K, Akashi S, Furuya M, Fukuhara K (1990) Rapid confirmation and revision of the primary structure of bovine serum-albumin by ESIMS and FRIT-FAB LC MS. Biochem Biophys Res Commun 173:639–646

    Article  PubMed  CAS  Google Scholar 

  13. Tsai CM, Frasch CE (1982) A sensitive silver stain for detecting lipopolysaccharides in polyacrylamide gels. Anal Biochem 119:115–119

    Article  PubMed  CAS  Google Scholar 

  14. Fodor G, Abidi S, Carpenter TC (1974) N-cyanoammonium salts as intermediates in the von Braun cyanogen bromide reaction. J Org Chem 39:1507–1516

    Article  CAS  Google Scholar 

  15. Aurell CA, Wistrom AO (1998) Critical aggregation concentrations of gram-negative bacterial lipopolysaccharides (LPS). Biochem Biophys Res Commun 253:119–123

    Article  PubMed  CAS  Google Scholar 

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Correspondence to Fernando Battaglini .

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Battaglini, F., Pallarola, D. (2011). Two Efficient Methods for the Conjugation of Smooth-Form Lipopolysaccharides with Probes Bearing Hydrazine or Amino Groups. I. LPS Activation with Cyanogen Bromide. In: Holst, O. (eds) Microbial Toxins. Methods in Molecular Biology, vol 739. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-61779-102-4_13

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  • DOI: https://doi.org/10.1007/978-1-61779-102-4_13

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  • Publisher Name: Humana Press, Totowa, NJ

  • Print ISBN: 978-1-61779-101-7

  • Online ISBN: 978-1-61779-102-4

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