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. 1996 Sep;3(5):541–546. doi: 10.1128/cdli.3.5.541-546.1996

Purification of Mycobacterium bovis BCG Tokyo antigens by chromatofocusing, lectin-affinity chromatography, and hydrophobic interaction chromatography.

E A Sugden 1, K Stilwell 1, D C Watson 1, E B Rohonczy 1, P Martineau 1
PMCID: PMC170403  PMID: 8877132

Abstract

A combination of chromatofocusing, lectin-affinity chromatography, and hydrophobic interaction chromatography resulted in a simple purification of protein antigens of Mycobacterium bovis BCG Tokyo culture filtrate. Identification was established on the basis of chromatographic separation, sodium dodecyl sulfate-polyacrylamide gel electrophoresis determination of molecular weights, and N-terminal amino acid determination. Chromatofocusing on PBE 94 accomplished the separation of BCG85B from other BCG85 complex antigens and partial separation of MPB64 and MPB70 antigens. Subsequently, MPB64 and MPB70 were completely separated on a high-performance liquid chromatography TSK Phenyl 5PW hydrophobic interaction chromatography column. This column also separated BCG85B from a 17-kDa protein with an N-terminal amino acid sequence of A-V-P-I-T-G-K-L-G-S-E-L-T-M-T-D-( )-V-G-Q, which is similar to the sequence of MPT63. Concanavalin A-Sepharose-affinity chromatography separated MPB64 from a 43- and 47-kDa doublet with an amino acid sequence of D-P-E-P-A-P-P-V-P-P-V-P-A-( )-A-A-S-P, which is similar to the sequence of MPT32 and which appears to be glycosylated.

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Selected References

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  1. Abou-Zeid C., Ratliff T. L., Wiker H. G., Harboe M., Bennedsen J., Rook G. A. Characterization of fibronectin-binding antigens released by Mycobacterium tuberculosis and Mycobacterium bovis BCG. Infect Immun. 1988 Dec;56(12):3046–3051. doi: 10.1128/iai.56.12.3046-3051.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Andersen A. B., Ljungqvist L., Hasløv K., Bentzon M. W. MPB 64 possesses 'tuberculosis-complex'-specific B- and T-cell epitopes. Scand J Immunol. 1991 Sep;34(3):365–372. doi: 10.1111/j.1365-3083.1991.tb01558.x. [DOI] [PubMed] [Google Scholar]
  3. Angus R. D. Production of reference PPD tuberculins for veterinary use in the United States. J Biol Stand. 1978 Jul;6(3):221–227. doi: 10.1016/s0092-1157(78)80008-0. [DOI] [PubMed] [Google Scholar]
  4. Bradford M. M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem. 1976 May 7;72:248–254. doi: 10.1016/0003-2697(76)90527-3. [DOI] [PubMed] [Google Scholar]
  5. Daniel T. M., Janicki B. W. Mycobacterial antigens: a review of their isolation, chemistry, and immunological properties. Microbiol Rev. 1978 Mar;42(1):84–113. doi: 10.1128/mr.42.1.84-113.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Daniel T. M. Tuberculin antigens: the need for purification. Am Rev Respir Dis. 1976 Jun;113(6):717–719. doi: 10.1164/arrd.1976.113.6.717. [DOI] [PubMed] [Google Scholar]
  7. De Bruyn J., Huygen K., Bosmans R., Fauville M., Lippens R., Van Vooren J. P., Falmagne P., Weckx M., Wiker H. G., Harboe M. Purification, characterization and identification of a 32 kDa protein antigen of Mycobacterium bovis BCG. Microb Pathog. 1987 May;2(5):351–366. doi: 10.1016/0882-4010(87)90077-5. [DOI] [PubMed] [Google Scholar]
  8. Dobos K. M., Swiderek K., Khoo K. H., Brennan P. J., Belisle J. T. Evidence for glycosylation sites on the 45-kilodalton glycoprotein of Mycobacterium tuberculosis. Infect Immun. 1995 Aug;63(8):2846–2853. doi: 10.1128/iai.63.8.2846-2853.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Drowart A., Launois P., De Cock M., Huygen K., De Bruyn J., Yernault J. C., Van Vooren J. P. An isoelectric focusing method for the study of the humoral response against the antigen 85 complex of Mycobacterium bovis BCG in the different forms of leprosy. J Immunol Methods. 1991 Dec 15;145(1-2):223–228. doi: 10.1016/0022-1759(91)90330-i. [DOI] [PubMed] [Google Scholar]
  10. Espitia C., Espinosa R., Saavedra R., Mancilla R., Romain F., Laqueyrerie A., Moreno C. Antigenic and structural similarities between Mycobacterium tuberculosis 50- to 55-kilodalton and Mycobacterium bovis BCG 45- to 47-kilodalton antigens. Infect Immun. 1995 Feb;63(2):580–584. doi: 10.1128/iai.63.2.580-584.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Espitia C., Mancilla R. Identification, isolation and partial characterization of Mycobacterium tuberculosis glycoprotein antigens. Clin Exp Immunol. 1989 Sep;77(3):378–383. [PMC free article] [PubMed] [Google Scholar]
  12. Espitia C., Sciutto E., Bottasso O., González-Amaro R., Hernández-Pando R., Mancilla R. High antibody levels to the mycobacterial fibronectin-binding antigen of 30-31 kD in tuberculosis and lepromatous leprosy. Clin Exp Immunol. 1992 Mar;87(3):362–367. doi: 10.1111/j.1365-2249.1992.tb03003.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Fifis T., Costopoulos C., Corner L. A., Wood P. R. Serological reactivity to Mycobacterium bovis protein antigens in cattle. Vet Microbiol. 1992 Mar;30(4):343–354. doi: 10.1016/0378-1135(92)90021-k. [DOI] [PubMed] [Google Scholar]
  14. Fifis T., Costopoulos C., Radford A. J., Bacic A., Wood P. R. Purification and characterization of major antigens from a Mycobacterium bovis culture filtrate. Infect Immun. 1991 Mar;59(3):800–807. doi: 10.1128/iai.59.3.800-807.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Godfrey H. P., Feng Z., Mandy S., Mandy K., Huygen K., De Bruyn J., Abou-Zeid C., Wiker H. G., Nagai S., Tasaka H. Modulation of expression of delayed hypersensitivity by mycobacterial antigen 85 fibronectin-binding proteins. Infect Immun. 1992 Jun;60(6):2522–2528. doi: 10.1128/iai.60.6.2522-2528.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Harboe M., Nagai S., Patarroyo M. E., Torres M. L., Ramirez C., Cruz N. Properties of proteins MPB64, MPB70, and MPB80 of Mycobacterium bovis BCG. Infect Immun. 1986 Apr;52(1):293–302. doi: 10.1128/iai.52.1.293-302.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Harboe M., Wiker H. G., Duncan J. R., Garcia M. M., Dukes T. W., Brooks B. W., Turcotte C., Nagai S. Protein G-based enzyme-linked immunosorbent assay for anti-MPB70 antibodies in bovine tuberculosis. J Clin Microbiol. 1990 May;28(5):913–921. doi: 10.1128/jcm.28.5.913-921.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Hasløv K., Andersen A. B., Bentzon M. W. Biological activity in sensitized guinea pigs of MPB 70, a protein specific for some strains of Mycobacterium bovis BCG. Scand J Immunol. 1987 Oct;26(4):445–454. doi: 10.1111/j.1365-3083.1987.tb02277.x. [DOI] [PubMed] [Google Scholar]
  19. Horwitz M. A., Lee B. W., Dillon B. J., Harth G. Protective immunity against tuberculosis induced by vaccination with major extracellular proteins of Mycobacterium tuberculosis. Proc Natl Acad Sci U S A. 1995 Feb 28;92(5):1530–1534. doi: 10.1073/pnas.92.5.1530. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
  21. Laqueyrerie A., Militzer P., Romain F., Eiglmeier K., Cole S., Marchal G. Cloning, sequencing, and expression of the apa gene coding for the Mycobacterium tuberculosis 45/47-kilodalton secreted antigen complex. Infect Immun. 1995 Oct;63(10):4003–4010. doi: 10.1128/iai.63.10.4003-4010.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Lin M., Sugden E. A., Jolley M. E., Stilwell K. Modification of the Mycobacterium bovis extracellular protein MPB70 with fluorescein for rapid detection of specific serum antibodies by fluorescence polarization. Clin Diagn Lab Immunol. 1996 Jul;3(4):438–443. doi: 10.1128/cdli.3.4.438-443.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Matsudaira P. Sequence from picomole quantities of proteins electroblotted onto polyvinylidene difluoride membranes. J Biol Chem. 1987 Jul 25;262(21):10035–10038. [PubMed] [Google Scholar]
  24. Miura K., Nagai S., Kinomoto M., Haga S., Tokunaga T. Comparative studies with various substrains of Mycobacterium bovis BCG on the production of an antigenic protein, MPB70. Infect Immun. 1983 Feb;39(2):540–545. doi: 10.1128/iai.39.2.540-545.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Nagai S., Matsumoto J., Nagasuga T. Specific skin-reactive protein from culture filtrate of Mycobacterium bovis BCG. Infect Immun. 1981 Mar;31(3):1152–1160. doi: 10.1128/iai.31.3.1152-1160.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Nagai S., Wiker H. G., Harboe M., Kinomoto M. Isolation and partial characterization of major protein antigens in the culture fluid of Mycobacterium tuberculosis. Infect Immun. 1991 Jan;59(1):372–382. doi: 10.1128/iai.59.1.372-382.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Patarroyo M. E., Parra C. A., Pinilla C., del Portillo P., Torres M. L., Clavijo P., Salazar L. M., Jimenez C. Immunogenic synthetic peptides against mycobacteria of potential immunodiagnostic and immunoprophylactic value. Lepr Rev. 1986 Dec;57 (Suppl 2):163–168. doi: 10.5935/0305-7518.19860068. [DOI] [PubMed] [Google Scholar]
  28. Romain F., Laqueyrerie A., Militzer P., Pescher P., Chavarot P., Lagranderie M., Auregan G., Gheorghiu M., Marchal G. Identification of a Mycobacterium bovis BCG 45/47-kilodalton antigen complex, an immunodominant target for antibody response after immunization with living bacteria. Infect Immun. 1993 Feb;61(2):742–750. doi: 10.1128/iai.61.2.742-750.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Salata R. A., Sanson A. J., Malhotra I. J., Wiker H. G., Harboe M., Phillips N. B., Daniel T. M. Purification and characterization of the 30,000 dalton native antigen of Mycobacterium tuberculosis and characterization of six monoclonal antibodies reactive with a major epitope of this antigen. J Lab Clin Med. 1991 Dec;118(6):589–598. [PubMed] [Google Scholar]
  30. Shapiro A. L., Viñuela E., Maizel J. V., Jr Molecular weight estimation of polypeptide chains by electrophoresis in SDS-polyacrylamide gels. Biochem Biophys Res Commun. 1967 Sep 7;28(5):815–820. doi: 10.1016/0006-291x(67)90391-9. [DOI] [PubMed] [Google Scholar]
  31. Smith P. K., Krohn R. I., Hermanson G. T., Mallia A. K., Gartner F. H., Provenzano M. D., Fujimoto E. K., Goeke N. M., Olson B. J., Klenk D. C. Measurement of protein using bicinchoninic acid. Anal Biochem. 1985 Oct;150(1):76–85. doi: 10.1016/0003-2697(85)90442-7. [DOI] [PubMed] [Google Scholar]
  32. Sugden E. A., Brooks B. W., Young N. M., Watson D. C., Nielsen K. H., Corner A. H., Turcotte C., Michaelides A., Stewart R. B. Chromatographic purification and characterization of antigens A and D from Mycobacterium paratuberculosis and their use in enzyme-linked immunosorbent assays for diagnosis of paratuberculosis in sheep. J Clin Microbiol. 1991 Aug;29(8):1659–1664. doi: 10.1128/jcm.29.8.1659-1664.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Sugden E. A., Samagh B. S., Bundle D. R., Duncan J. R. Lipoarabinomannan and lipid-free arabinomannan antigens of Mycobacterium paratuberculosis. Infect Immun. 1987 Mar;55(3):762–770. doi: 10.1128/iai.55.3.762-770.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Wieles B., van Agterveld M., Janson A., Clark-Curtiss J., Rinke de Wit T., Harboe M., Thole J. Characterization of a Mycobacterium leprae antigen related to the secreted Mycobacterium tuberculosis protein MPT32. Infect Immun. 1994 Jan;62(1):252–258. doi: 10.1128/iai.62.1.252-258.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Wiker H. G., Harboe M., Lea T. E. Purification and characterization of two protein antigens from the heterogeneous BCG85 complex in Mycobacterium bovis BCG. Int Arch Allergy Appl Immunol. 1986;81(4):298–306. doi: 10.1159/000234153. [DOI] [PubMed] [Google Scholar]
  36. Wiker H. G., Harboe M., Nagai S., Patarroyo M. E., Ramirez C., Cruz N. MPB59, a widely cross-reacting protein of Mycobacterium bovis BCG. Int Arch Allergy Appl Immunol. 1986;81(4):307–314. doi: 10.1159/000234154. [DOI] [PubMed] [Google Scholar]
  37. Wiker H. G., Harboe M. The antigen 85 complex: a major secretion product of Mycobacterium tuberculosis. Microbiol Rev. 1992 Dec;56(4):648–661. doi: 10.1128/mr.56.4.648-661.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Wiker H. G., Sletten K., Nagai S., Harboe M. Evidence for three separate genes encoding the proteins of the mycobacterial antigen 85 complex. Infect Immun. 1990 Jan;58(1):272–274. doi: 10.1128/iai.58.1.272-274.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]

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