Characterization of the Menkes protein copper-binding domains and their role in copper-induced protein relocalization.

Menkes disease is a fatal X-linked disorder of copper metabolism. The gene defective in Menkes disease (ATP7A) encodes a copper transporting P-type ATPase (MNK or ATP7A) with six copper-binding domains at its N-terminus. MNK is normally localized to the trans -Golgi network in cultured cells, but re...

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Main Authors: Goodyer, I, Jones, E, Monaco, A, Francis, M
Format: Journal article
Language:English
Published: Oxford University Press 1999
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author Goodyer, I
Jones, E
Monaco, A
Francis, M
author_facet Goodyer, I
Jones, E
Monaco, A
Francis, M
author_sort Goodyer, I
collection OXFORD
description Menkes disease is a fatal X-linked disorder of copper metabolism. The gene defective in Menkes disease (ATP7A) encodes a copper transporting P-type ATPase (MNK or ATP7A) with six copper-binding domains at its N-terminus. MNK is normally localized to the trans -Golgi network in cultured cells, but relocates to the plasma membrane in the presence of elevated extracellular copper. In this study, the role of the six copper-binding domains on copper-induced redistribution is investigated. In a recombinant clone, when all the wild-type copper-binding motifs are mutated from GMXCXXC to GMXSXXS and the cells grown in medium containing elevated copper, relocalization of the recombinant protein to the plasma membrane was not observed. Using the same assay with any one of the six copper-binding domains intact, MNK moves to the plasma membrane in a way indistinguishable from the wild-type protein. Therefore, the copper-binding domains are vital for MNK trafficking and only a single domain is sufficient for this redistribution to occur.
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spelling oxford-uuid:29a59e87-39a5-4401-8472-f525e585570f2022-03-26T12:20:23ZCharacterization of the Menkes protein copper-binding domains and their role in copper-induced protein relocalization.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:29a59e87-39a5-4401-8472-f525e585570fEnglishSymplectic Elements at OxfordOxford University Press1999Goodyer, IJones, EMonaco, AFrancis, MMenkes disease is a fatal X-linked disorder of copper metabolism. The gene defective in Menkes disease (ATP7A) encodes a copper transporting P-type ATPase (MNK or ATP7A) with six copper-binding domains at its N-terminus. MNK is normally localized to the trans -Golgi network in cultured cells, but relocates to the plasma membrane in the presence of elevated extracellular copper. In this study, the role of the six copper-binding domains on copper-induced redistribution is investigated. In a recombinant clone, when all the wild-type copper-binding motifs are mutated from GMXCXXC to GMXSXXS and the cells grown in medium containing elevated copper, relocalization of the recombinant protein to the plasma membrane was not observed. Using the same assay with any one of the six copper-binding domains intact, MNK moves to the plasma membrane in a way indistinguishable from the wild-type protein. Therefore, the copper-binding domains are vital for MNK trafficking and only a single domain is sufficient for this redistribution to occur.
spellingShingle Goodyer, I
Jones, E
Monaco, A
Francis, M
Characterization of the Menkes protein copper-binding domains and their role in copper-induced protein relocalization.
title Characterization of the Menkes protein copper-binding domains and their role in copper-induced protein relocalization.
title_full Characterization of the Menkes protein copper-binding domains and their role in copper-induced protein relocalization.
title_fullStr Characterization of the Menkes protein copper-binding domains and their role in copper-induced protein relocalization.
title_full_unstemmed Characterization of the Menkes protein copper-binding domains and their role in copper-induced protein relocalization.
title_short Characterization of the Menkes protein copper-binding domains and their role in copper-induced protein relocalization.
title_sort characterization of the menkes protein copper binding domains and their role in copper induced protein relocalization
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AT jonese characterizationofthemenkesproteincopperbindingdomainsandtheirroleincopperinducedproteinrelocalization
AT monacoa characterizationofthemenkesproteincopperbindingdomainsandtheirroleincopperinducedproteinrelocalization
AT francism characterizationofthemenkesproteincopperbindingdomainsandtheirroleincopperinducedproteinrelocalization