The role of the invariant His-1069 in folding and function of the Wilson's disease protein, the human copper-transporting ATPase ATP7B

Ruslan Tsivkovskii, Roman G. Efremov, Svetlana Lutsenko

Research output: Contribution to journalArticle

Abstract

The copper-transporting ATPase ATP7B is essential for normal distribution of copper in human cells. Mutations in ATP7B lead to Wilson's disease, a severe disorder with neurological and hepatic manifestations. One of the most common disease mutations, a H1069Q substitution, causes intracellular mislocalization of ATP7B (the Wilson's disease protein, WNDP). His-1069 is located in the nucleotide-binding domain of WNDP and is conserved in all copper-transporting ATPases from bacteria to mammals; however, the specific role of this His in the structure and function of WNDP remains unclear. We demonstrate that substitution of His-1069 for Gln, Ala, or Cys does not significantly alter the folding of the WNDP nucleotide-binding domain or the proteolytic resistance of the full-length WNDP. In contrast, the function of WNDP is markedly affected by the mutations. The ability to form an acylphosphate intermediate in the presence of ATP is entirely lost in all three mutants, suggesting that His-1069 is important for ATP-dependent phosphorylation. Other steps of the WNDP enzymatic cycle are less dependent on His-1069. The H1069C mutant shows normal phosphorylation in the presence of inorganic phosphate; it binds an ATP analogue, β,γ-imidoadenosine 5′-triphosphate (AMP-PNP), and copper and undergoes nucleotide-dependent conformational transitions similar to those of the wild-type WNDP. Although binding of AMP-PNP is not disrupted by the mutation, the apparent affinity for the nucleotide is decreased by 4-fold. We conclude that His-1069 is responsible for proper orientation of ATP in the catalytic site of WNDP prior to ATP hydrolysis.

Original languageEnglish (US)
Pages (from-to)13302-13308
Number of pages7
JournalJournal of Biological Chemistry
Volume278
Issue number15
DOIs
StatePublished - Apr 11 2003
Externally publishedYes

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Adenosine Triphosphate
Nucleotides
Adenylyl Imidodiphosphate
Mutation
Phosphorylation
Copper
Substitution reactions
Wilson disease protein
copper-transporting ATPases
Hepatolenticular Degeneration
Mammals
Normal Distribution
Normal distribution
Neurologic Manifestations
Protein Binding
Hydrolysis
Catalytic Domain
Bacteria
Phosphates
Cells

ASJC Scopus subject areas

  • Biochemistry

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The role of the invariant His-1069 in folding and function of the Wilson's disease protein, the human copper-transporting ATPase ATP7B. / Tsivkovskii, Ruslan; Efremov, Roman G.; Lutsenko, Svetlana.

In: Journal of Biological Chemistry, Vol. 278, No. 15, 11.04.2003, p. 13302-13308.

Research output: Contribution to journalArticle

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