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THE SPECIFICITY OF KERATEINE DERIVATIVES

Carboxymethyl, α-carboxyethyl-, α-carboxy-n-propyl-, α-carboxyisopropyl-, α-carboxy-n-butyl, α-carboxyisobutyl, α-carboxyamyl-, benzyl-, and β-phenylethylkeratemes were prepared from the parent protein, reduced keratin or kerateine. Chemical analysis disclosed that the various compounds differed in...

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Detalles Bibliográficos
Autores principales: Pillemer, L., Ecker, E. E., Martiensen, E. W.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1939
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2133800/
https://www.ncbi.nlm.nih.gov/pubmed/19870917
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author Pillemer, L.
Ecker, E. E.
Martiensen, E. W.
author_facet Pillemer, L.
Ecker, E. E.
Martiensen, E. W.
author_sort Pillemer, L.
collection PubMed
description Carboxymethyl, α-carboxyethyl-, α-carboxy-n-propyl-, α-carboxyisopropyl-, α-carboxy-n-butyl, α-carboxyisobutyl, α-carboxyamyl-, benzyl-, and β-phenylethylkeratemes were prepared from the parent protein, reduced keratin or kerateine. Chemical analysis disclosed that the various compounds differed in their isoelectric points and solubilities depending on the nature of the substituent group introduced. In general, it was found that in so far as could be determined, nearly all of the available sulfhydryl groups were substituted, while no detectable substitution of the free amino groups of the proteins occurred. The results of the serologic studies revealed that the kerateine derivatives acquired a new immunologie character dependent on the nature of the introduced determinant group. Inhibition tests confirmed the results obtained. Evidence was also produced to show that the grouping See PDF for structure may play a rôle in some of the reactions observed.
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spelling pubmed-21338002008-04-18 THE SPECIFICITY OF KERATEINE DERIVATIVES Pillemer, L. Ecker, E. E. Martiensen, E. W. J Exp Med Article Carboxymethyl, α-carboxyethyl-, α-carboxy-n-propyl-, α-carboxyisopropyl-, α-carboxy-n-butyl, α-carboxyisobutyl, α-carboxyamyl-, benzyl-, and β-phenylethylkeratemes were prepared from the parent protein, reduced keratin or kerateine. Chemical analysis disclosed that the various compounds differed in their isoelectric points and solubilities depending on the nature of the substituent group introduced. In general, it was found that in so far as could be determined, nearly all of the available sulfhydryl groups were substituted, while no detectable substitution of the free amino groups of the proteins occurred. The results of the serologic studies revealed that the kerateine derivatives acquired a new immunologie character dependent on the nature of the introduced determinant group. Inhibition tests confirmed the results obtained. Evidence was also produced to show that the grouping See PDF for structure may play a rôle in some of the reactions observed. The Rockefeller University Press 1939-09-30 /pmc/articles/PMC2133800/ /pubmed/19870917 Text en Copyright © Copyright, 1939, by The Rockefeller Institute for Medical Research New York 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
Pillemer, L.
Ecker, E. E.
Martiensen, E. W.
THE SPECIFICITY OF KERATEINE DERIVATIVES
title THE SPECIFICITY OF KERATEINE DERIVATIVES
title_full THE SPECIFICITY OF KERATEINE DERIVATIVES
title_fullStr THE SPECIFICITY OF KERATEINE DERIVATIVES
title_full_unstemmed THE SPECIFICITY OF KERATEINE DERIVATIVES
title_short THE SPECIFICITY OF KERATEINE DERIVATIVES
title_sort specificity of kerateine derivatives
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2133800/
https://www.ncbi.nlm.nih.gov/pubmed/19870917
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