Literature DB >> 3361137

Immunoblot analysis of the eighth component of human complement. Demonstration of subunits and detection of C8 alpha-gamma double and triple bands.

W Nürnberger1, R Seger, P Kobler, I Mons, F Tedesco, V Wahn.   

Abstract

Using SDS-PAGE/immunoblot analysis of the eighth component of human complement, C8, we have been able to demonstrate an 85 kDa C8 alpha-gamma and a 62 kDa C8 beta subunit in normal human serum. Serum from an undiagnosed patient who presented undetectable hemolytic C8 activity possessed only the 85 kDa subunit, suggesting a defect in the C8 beta subunit. Serum of a patient with known C8 alpha-gamma deficiency possessed only the complementary 62 kDa subunit. Both sera used together were able to lyse antibody-sensitized sheep erythrocytes, whereas individual sera could not. Optimum conditions for C8 immunoblotting were determined using small amounts of serum or plasma, during low voltage electrophoresis and a sensitive staining technique (nitrobluetetrazolium/bromochloroindoxylphosphate). Using these conditions, the C8 alpha-gamma subunit was found to be composed of up to three bands, termed C8 alpha-gamma 1, -2 and -3. All three bands were found in pooled normal sera. Individual sera had at least the C8 alpha-gamma 2 and C8 alpha-gamma 3 bands. Two C8 beta-deficient sera from two unrelated patients exhibited only the C8 alpha-gamma 2 and C8 alpha-gamma 3 bands. We conclude that immunoblotting of C8 permits a detailed analysis of the molecular composition of this component and helps to establish a precise diagnosis in inherited C8 deficiencies.

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Year:  1988        PMID: 3361137     DOI: 10.1016/0022-1759(88)90251-7

Source DB:  PubMed          Journal:  J Immunol Methods        ISSN: 0022-1759            Impact factor:   2.303


  2 in total

1.  A case of hereditary combined deficiency of complement components C6 and C7 in man.

Authors:  B P Morgan; J P Vora; A J Bennett; J P Thomas; N Matthews
Journal:  Clin Exp Immunol       Date:  1989-03       Impact factor: 4.330

2.  Familial deficiency of the seventh component of complement associated with recurrent meningococcal infections.

Authors:  W Nürnberger; H Pietsch; R Seger; T Bufon; V Wahn
Journal:  Eur J Pediatr       Date:  1989-08       Impact factor: 3.183

  2 in total

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