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The aging-associated enzyme CLK-1 is a member of the carboxylate-bridged diiron family of proteins.
Behan, Rachel K; Lippard, Stephen J.
Affiliation
  • Behan RK; Department of Chemistry, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, United States.
Biochemistry ; 49(45): 9679-81, 2010 Nov 16.
Article in En | MEDLINE | ID: mdl-20923139
ABSTRACT
The aging-associated enzyme CLK-1 is proposed to be a member of the carboxylate-bridged diiron family of proteins. To evaluate this hypothesis and characterize the protein, we expressed soluble mouse CLK-1 (MCLK1) in Escherichia coli as a heterologous host. Using Mössbauer and EPR spectroscopy, we established that MCLK1 indeed belongs to this protein family. Biochemical analyses of the in vitro activity of MCLK1 with quinone substrates revealed that NADH can serve directly as a reductant for catalytic activation of dioxygen and substrate oxidation by the enzyme, with no requirement for an additional reductase protein component. The direct reaction of NADH with a diiron-containing oxidase enzyme has not previously been encountered for any member of the protein superfamily.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Mitochondrial Proteins / Membrane Proteins Type of study: Risk_factors_studies Limits: Animals Language: En Journal: Biochemistry Year: 2010 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Mitochondrial Proteins / Membrane Proteins Type of study: Risk_factors_studies Limits: Animals Language: En Journal: Biochemistry Year: 2010 Document type: Article Affiliation country: United States