Literature DB >> 6245139

Life-span and size of the trans-membrane channel formed by large doses of complement.

L E Ramm, M M Mayer.   

Abstract

To evaluate the life-span and size of trans-membrane channels in complement (C) treated membranes, resealed erythrocyte ghosts containing trapped native protein markers, as well as residual hemoglobin, were treated with anti-Forssman antibody and large doses of guinea pig C. Ovalbumin and hemoglobin were released slowly through the channels so produced, whereas human serum albumin was not. Release of hemoglobin was not blocked by extracellular bovine serum albumin. Release of hemoglobin continued for at least 72 hr at 4 degrees C. Semi-logarithmic plots of ovalbumin or hemoglobin release showed gradual diminution of the rate constant, which indicates slow loss of channels during the experimental period. These experiments demonstrate that the channels produced in erythrocyte ghost membranes by large C doses have a long, although finite, life-span. Their effective diameter is al least 55 A on the basis of ovalbumin and hemoglobin release, and not more than 150 A, since serum albumin was not released. However, an upper limit of 100 A would be more reasonable in light of electronmicroscopic observations by others. These results are compatible with the doughnut model.

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Year:  1980        PMID: 6245139

Source DB:  PubMed          Journal:  J Immunol        ISSN: 0022-1767            Impact factor:   5.422


  18 in total

1.  Complement pore genesis observed in erythrocyte membranes by fluorescence microscopic single-channel recording.

Authors:  H Sauer; L Pratsch; G Fritzsch; S Bhakdi; R Peters
Journal:  Biochem J       Date:  1991-06-01       Impact factor: 3.857

2.  Complement action on secretory cells identified by the reverse hemolytic plaque assay: modified assay eliminates exposure of secretory cells to complement.

Authors:  K A Gregerson
Journal:  Endocrine       Date:  1995-05       Impact factor: 3.633

Review 3.  Complement membrane attack on nucleated cells: resistance, recovery and non-lethal effects.

Authors:  B P Morgan
Journal:  Biochem J       Date:  1989-11-15       Impact factor: 3.857

4.  Complement induces a transient increase in membrane permeability in unlysed erythrocytes.

Authors:  J A Halperin; A Nicholson-Weller; C Brugnara; D C Tosteson
Journal:  J Clin Invest       Date:  1988-08       Impact factor: 14.808

5.  Single channel currents induced by complement in antibody-coated cell membranes.

Authors:  M B Jackson; C L Stephens; H Lecar
Journal:  Proc Natl Acad Sci U S A       Date:  1981-10       Impact factor: 11.205

Review 6.  The membrane attack complex.

Authors:  H J Müller-Eberhard
Journal:  Springer Semin Immunopathol       Date:  1984

Review 7.  Is the membrane attack complex of complement an enzyme?

Authors:  M D Boyle
Journal:  Mol Cell Biochem       Date:  1984       Impact factor: 3.396

8.  Transmembrane channel formation by complement: functional analysis of the number of C5b6, C7, C8, and C9 molecules required for a single channel.

Authors:  L E Ramm; M B Whitlow; M M Mayer
Journal:  Proc Natl Acad Sci U S A       Date:  1982-08       Impact factor: 11.205

9.  Polymerization of the ninth component of complement (C9): formation of poly(C9) with a tubular ultrastructure resembling the membrane attack complex of complement.

Authors:  E R Podack; J Tschopp
Journal:  Proc Natl Acad Sci U S A       Date:  1982-01       Impact factor: 11.205

Review 10.  Killing machines: three pore-forming proteins of the immune system.

Authors:  Ryan McCormack; Lesley de Armas; Motoaki Shiratsuchi; Eckhard R Podack
Journal:  Immunol Res       Date:  2013-12       Impact factor: 2.829

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