Identification and drug binding capabilities of tubulin in the nematode Ascaridia galli.

Cell extracts of Ascaridia galli bind colchicine in a manner suggesting the presence of a tubulin-like protein. Column chromatography of these extracts on DEAE-Sephadex yielded only one peak with colchicine-binding activity. Single peaks of radioactivity in this same position were obtained on chroma...

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Main Authors: Ireland, C, Clayton, L, Gutteridge, W, Pogson, C, Gull, K
Format: Journal article
Language:English
Published: 1982
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author Ireland, C
Clayton, L
Gutteridge, W
Pogson, C
Gull, K
author_facet Ireland, C
Clayton, L
Gutteridge, W
Pogson, C
Gull, K
author_sort Ireland, C
collection OXFORD
description Cell extracts of Ascaridia galli bind colchicine in a manner suggesting the presence of a tubulin-like protein. Column chromatography of these extracts on DEAE-Sephadex yielded only one peak with colchicine-binding activity. Single peaks of radioactivity in this same position were obtained on chromatography of extracts prelabelled with either [3H]colchicine or [3H]parbendazole. Sodium dodecyl sulphate polyacrylamide gel electrophoresis and two dimensional gel electrophoresis of the fractions making up the peaks indicated the presence of two proteins which co-migrate with mammalian brain alpha- and beta-tubulin markers. More detailed investigation showed that the A. galli tubulin has a slightly different alpha-subunit when compared with mammalian tubulin.
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spelling oxford-uuid:12a3e66c-009f-49f1-82c8-01b088e193b42022-03-26T10:08:59ZIdentification and drug binding capabilities of tubulin in the nematode Ascaridia galli.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:12a3e66c-009f-49f1-82c8-01b088e193b4EnglishSymplectic Elements at Oxford1982Ireland, CClayton, LGutteridge, WPogson, CGull, KCell extracts of Ascaridia galli bind colchicine in a manner suggesting the presence of a tubulin-like protein. Column chromatography of these extracts on DEAE-Sephadex yielded only one peak with colchicine-binding activity. Single peaks of radioactivity in this same position were obtained on chromatography of extracts prelabelled with either [3H]colchicine or [3H]parbendazole. Sodium dodecyl sulphate polyacrylamide gel electrophoresis and two dimensional gel electrophoresis of the fractions making up the peaks indicated the presence of two proteins which co-migrate with mammalian brain alpha- and beta-tubulin markers. More detailed investigation showed that the A. galli tubulin has a slightly different alpha-subunit when compared with mammalian tubulin.
spellingShingle Ireland, C
Clayton, L
Gutteridge, W
Pogson, C
Gull, K
Identification and drug binding capabilities of tubulin in the nematode Ascaridia galli.
title Identification and drug binding capabilities of tubulin in the nematode Ascaridia galli.
title_full Identification and drug binding capabilities of tubulin in the nematode Ascaridia galli.
title_fullStr Identification and drug binding capabilities of tubulin in the nematode Ascaridia galli.
title_full_unstemmed Identification and drug binding capabilities of tubulin in the nematode Ascaridia galli.
title_short Identification and drug binding capabilities of tubulin in the nematode Ascaridia galli.
title_sort identification and drug binding capabilities of tubulin in the nematode ascaridia galli
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