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THE KINETICS OF INACTIVATION OF COMPLEMENT BY LIGHT

The photoinactivation of complement has been studied with a view to determining if possible how many kinds of molecules disappeared during the reaction. It was found that: 1. The apparent course of photoinactivation is that of a monomolecular reaction. 2. Diffusion is not the limiting factor respons...

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Autor principal: Brooks, S. C.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1920
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2140422/
https://www.ncbi.nlm.nih.gov/pubmed/19871855
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author Brooks, S. C.
author_facet Brooks, S. C.
author_sort Brooks, S. C.
collection PubMed
description The photoinactivation of complement has been studied with a view to determining if possible how many kinds of molecules disappeared during the reaction. It was found that: 1. The apparent course of photoinactivation is that of a monomolecular reaction. 2. Diffusion is not the limiting factor responsible for this fact, because the temperature coefficient of diffusion is much higher than that of photoinactivation (Q (10) = 1.22 to 1.28, and Q (10) = 1.10 respectively). 3. There is no change in the transparency of serum solutions during photoinactivation, at least for light of the effective wave-length, which is in the ultra-violet region probably at about 2530 Ångström units. It is pointed out that under these conditions only one interpretation is possible; namely, that during photoinactivation a single disappearing molecular species governs the rate of reaction. This substance must be primarily responsible for the hemolytic power of serum when it is used as complement.
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spelling pubmed-21404222008-04-23 THE KINETICS OF INACTIVATION OF COMPLEMENT BY LIGHT Brooks, S. C. J Gen Physiol Article The photoinactivation of complement has been studied with a view to determining if possible how many kinds of molecules disappeared during the reaction. It was found that: 1. The apparent course of photoinactivation is that of a monomolecular reaction. 2. Diffusion is not the limiting factor responsible for this fact, because the temperature coefficient of diffusion is much higher than that of photoinactivation (Q (10) = 1.22 to 1.28, and Q (10) = 1.10 respectively). 3. There is no change in the transparency of serum solutions during photoinactivation, at least for light of the effective wave-length, which is in the ultra-violet region probably at about 2530 Ångström units. It is pointed out that under these conditions only one interpretation is possible; namely, that during photoinactivation a single disappearing molecular species governs the rate of reaction. This substance must be primarily responsible for the hemolytic power of serum when it is used as complement. The Rockefeller University Press 1920-11-20 /pmc/articles/PMC2140422/ /pubmed/19871855 Text en Copyright © Copyright, 1920, by The Rockefeller Institute for Medical Research 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
Brooks, S. C.
THE KINETICS OF INACTIVATION OF COMPLEMENT BY LIGHT
title THE KINETICS OF INACTIVATION OF COMPLEMENT BY LIGHT
title_full THE KINETICS OF INACTIVATION OF COMPLEMENT BY LIGHT
title_fullStr THE KINETICS OF INACTIVATION OF COMPLEMENT BY LIGHT
title_full_unstemmed THE KINETICS OF INACTIVATION OF COMPLEMENT BY LIGHT
title_short THE KINETICS OF INACTIVATION OF COMPLEMENT BY LIGHT
title_sort kinetics of inactivation of complement by light
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2140422/
https://www.ncbi.nlm.nih.gov/pubmed/19871855
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