Identification and characterization of an 8-kDa light chain associated with Dictyostelium discoideum MyoB, a class I myosin

Abstract

Dictyostelium discoideum MyoB is a single-headed class I myosin. Analysis of purified MyoB by SDS-PAGE indicated the presence of an ∼9-kDa light chain. A tryptic digest of MyoB yielded a partial sequence for the light chain that exactly matched a sequence in a 73-amino acid, 8,296-Da protein (dictyBase number DDB0188713). This protein, termed MlcB, contains two EF-hand motifs and shares ∼30% sequence identity with the N- and C-terminal lobes of calmodulin. FLAG-MlcB expressed in Dictyostelium co-immunoprecipitated with MyoB but not with the related class I myosins MyoC and MyoD. Recombinant MlcB bound Ca2+/ with a Kd value of 0.2 μM and underwent a Ca 2+/-induced change in conformation that increased α-helical content and surface hydrophobicity. Mutational analysis showed that the first EF-hand was responsible for Ca2+/ binding. In the presence and absence of Ca2+/ MlcB was a monomer in solution and bound to a MyoB IQ motif peptide with a Kd value of ∼0.5 μM. A MyoB head-neck construct with a Ser to Glu mutation at the TEDS site bound MlcB and displayed an actin-activated Mg2+/ ATPase activity that was insensitive to Ca2+/. We conclude that MlcB represents a novel type of small myosin light chain that binds to IQ motifs in amanner comparable with a single lobe of a typical four-EF-hand protein. © 2006 by The American Society for Biochemistry and Molecular Biology, Inc.