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PROPERDIN FACTOR D : II. ACTIVATION TO D BY PROPERDIN

The protein in the properdin pathway responsible for conversion of precursor factor D to D has been isolated and found to be identical with properdin. Sequential ion exchange and gel filtration chromatography demonstrated identity between properdin protein, measured by radial immunodiffusion, and th...

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Detalles Bibliográficos
Autores principales: Fearon, Douglas T., Austen, K. Frank, Ruddy, Shaun
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1974
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2139584/
https://www.ncbi.nlm.nih.gov/pubmed/4211020
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author Fearon, Douglas T.
Austen, K. Frank
Ruddy, Shaun
author_facet Fearon, Douglas T.
Austen, K. Frank
Ruddy, Shaun
author_sort Fearon, Douglas T.
collection PubMed
description The protein in the properdin pathway responsible for conversion of precursor factor D to D has been isolated and found to be identical with properdin. Sequential ion exchange and gel filtration chromatography demonstrated identity between properdin protein, measured by radial immunodiffusion, and the capacity to activate D to D, assessed by formation of the intermediate, EAC43B(D). Properdin, purified in this manner, was homogeneous on acid polyacrylamide disc gel electrophoretic analysis, with the band of protein corresponding to the position of eluates in the replicate gel capable of activating highly purified D. Demonstration of the homogeneity of purified D by alkaline disc gel electrophoresis, coupled with the linear stoichiometric hemolytic titrations of each factor, indicates that direct interaction between properdin and D generates D. Thus, activation of D by properdin represents a mechanism in the properdin pathway by which D becomes available for formation of the C3b-dependent C3 convertase.
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spelling pubmed-21395842008-04-17 PROPERDIN FACTOR D : II. ACTIVATION TO D BY PROPERDIN Fearon, Douglas T. Austen, K. Frank Ruddy, Shaun J Exp Med Article The protein in the properdin pathway responsible for conversion of precursor factor D to D has been isolated and found to be identical with properdin. Sequential ion exchange and gel filtration chromatography demonstrated identity between properdin protein, measured by radial immunodiffusion, and the capacity to activate D to D, assessed by formation of the intermediate, EAC43B(D). Properdin, purified in this manner, was homogeneous on acid polyacrylamide disc gel electrophoretic analysis, with the band of protein corresponding to the position of eluates in the replicate gel capable of activating highly purified D. Demonstration of the homogeneity of purified D by alkaline disc gel electrophoresis, coupled with the linear stoichiometric hemolytic titrations of each factor, indicates that direct interaction between properdin and D generates D. Thus, activation of D by properdin represents a mechanism in the properdin pathway by which D becomes available for formation of the C3b-dependent C3 convertase. The Rockefeller University Press 1974-08-01 /pmc/articles/PMC2139584/ /pubmed/4211020 Text en Copyright © 1974 by The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Article
Fearon, Douglas T.
Austen, K. Frank
Ruddy, Shaun
PROPERDIN FACTOR D : II. ACTIVATION TO D BY PROPERDIN
title PROPERDIN FACTOR D : II. ACTIVATION TO D BY PROPERDIN
title_full PROPERDIN FACTOR D : II. ACTIVATION TO D BY PROPERDIN
title_fullStr PROPERDIN FACTOR D : II. ACTIVATION TO D BY PROPERDIN
title_full_unstemmed PROPERDIN FACTOR D : II. ACTIVATION TO D BY PROPERDIN
title_short PROPERDIN FACTOR D : II. ACTIVATION TO D BY PROPERDIN
title_sort properdin factor d : ii. activation to d by properdin
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2139584/
https://www.ncbi.nlm.nih.gov/pubmed/4211020
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