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FEBS Lett ; 591(8): 1176-1186, 2017 04.
Article in English | MEDLINE | ID: mdl-28295264

ABSTRACT

We identified the Grb7 family members, Grb10 and Grb14, as Ca2+ -dependent CaM-binding proteins using Ca2+ -dependent CaM-affinity chromatography as we previously did with Grb7. The potential CaM-binding sites were identified and experimentally tested using fluorescent-labeled peptides corresponding to these sites. The apparent affinity constant of these peptides for CaM, and the minimum number of calcium ions bound to CaM that are required for effective binding to these peptides were also determined. We prepared deletion mutants of the three adaptor proteins lacking the identified sites and determined that they lost or strongly diminished their CaM-binding capacity following the sequence Grb7 > > Grb14 > Grb10. More than one CaM-binding site and/or accessory CaM-binding sites appear to exist in Grb10 and Grb14, as compared to a single one present in Grb7.


Subject(s)
Adaptor Proteins, Signal Transducing/metabolism , Calcium Signaling , Calmodulin/metabolism , GRB10 Adaptor Protein/metabolism , Adaptor Proteins, Signal Transducing/chemistry , Adaptor Proteins, Signal Transducing/genetics , Amino Acid Sequence , Binding Sites , Calmodulin/chemistry , Chromatography, Affinity , Conserved Sequence , GRB10 Adaptor Protein/chemistry , GRB10 Adaptor Protein/genetics , GRB7 Adaptor Protein/chemistry , GRB7 Adaptor Protein/genetics , GRB7 Adaptor Protein/metabolism , Gene Deletion , HEK293 Cells , Humans , Kinetics , Mutagenesis, Site-Directed , Peptide Fragments/chemistry , Peptide Fragments/genetics , Peptide Fragments/metabolism , Protein Conformation , Protein Interaction Domains and Motifs , Recombinant Fusion Proteins/chemistry , Recombinant Fusion Proteins/metabolism , Sequence Homology, Amino Acid , Structural Homology, Protein
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