1. Identification of a novel zinc-binding protein, C1orf123, as an interactor with a heavy metal-associated domain
- Author
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Takehiko Tosha, Kenta Nakagome, Tomoaki Hagai, Yoshiaki Furukawa, Carolyn T. Lim, Shoji Watanabe, Yoshitsugu Shiro, Koki Yoshida, and Shuji Akiyama
- Subjects
0301 basic medicine ,Models, Molecular ,lcsh:Medicine ,Plasma protein binding ,01 natural sciences ,Biochemistry ,Physical Chemistry ,Protein Structure, Secondary ,Protein structure ,Yeast Two-Hybrid Assays ,Two-Hybrid Screening ,lcsh:Science ,Peptide sequence ,Multidisciplinary ,Crystallography ,biology ,Chemistry ,Physics ,Condensed Matter Physics ,Solutions ,Copper chaperone for superoxide dismutase ,Zinc ,Physical Sciences ,Crystal Structure ,Protein Interaction Assays ,Research Article ,Chemical Elements ,Protein Binding ,Cations, Divalent ,Protein domain ,Static Electricity ,Computational biology ,Library Screening ,010402 general chemistry ,Research and Analysis Methods ,Protein–protein interaction ,03 medical and health sciences ,Structure-Activity Relationship ,Protein Domains ,Metals, Heavy ,Two-Hybrid System Techniques ,Escherichia coli ,Solid State Physics ,Humans ,Amino Acid Sequence ,Molecular Biology Techniques ,Protein Interactions ,Molecular Biology ,Molecular Biology Assays and Analysis Techniques ,Chemical Bonding ,Superoxide Dismutase ,lcsh:R ,Biology and Life Sciences ,Proteins ,Membrane Transport Proteins ,Hydrogen Bonding ,HMA domain ,0104 chemical sciences ,Open reading frame ,030104 developmental biology ,lcsh:Q ,biology.gene ,Copper - Abstract
Heavy metal-associated (HMA) domains bind metal ions at its Cys-x-x-Cys (CxxC) motif and constitute an intracellular network for trafficking of metal ions for utilization and detoxification. We thus expect that novel metalloproteins can be identified by screening proteins interacting with a HMA domain. In this study, we performed yeast two-hybrid screening of the human proteome and found an uncharacterized protein encoded as open reading frame 123 in chromosome 1 (C1orf123) that can interact specifically with the HMA domain of a copper chaperone for superoxide dismutase (CCSdI). Our X-ray structural analysis of C1orf123 further revealed that it binds a Zn2+ ion in a tetrahedral coordination with four thiolate groups from two conserved CxxC motifs. For the interaction between C1orf123 and CCSdI, the CxxC motifs in both C1orf123 and CCSdI were required, implying metal-mediated interaction through the CxxC motifs. Notably, C1orf123 did not interact with several other HMA domains containing CxxC motifs, supporting high specificity in the interaction between C1orf123 and CCSdI. Based upon these results, we further discuss functional and structural significance of the interaction between C1orf123 and CCS.
- Published
- 2018