Unidirectional growth of heavy meromyosin clusters along actin filaments revealed by real‐time fluorescence microscopy. Issue 12 (24th October 2017)

• Record Type: Journal Article
• Authors: Hirakawa, Rika; Nishikawa, Yusuke; Uyeda, Taro Q.P.; Tokuraku, Kiyotaka
• Is Part Of: Cytoskeleton. Volume 74:Issue 12(2017)
• Page Start: 482
• Page End: 489
• Publication Date: 2017-10-24
• Subjects: acto‐S1dC chimera -- allosteric regulation -- cofilin -- cooperative binding -- myosin II; Cytoskeleton -- Periodicals; 571.65405
• DOI: 10.1002/cm.21408
• Languages: English
• ISSNs: 1949-3584

Abstract

Abstract: Heavy meromyosin (HMM) forms clusters along actin filaments under low ATP concentrations. Here, we observed the growth of HMM clusters under low concentrations of ATP in real time using fluorescence microscopy. When actin filaments were loosely immobilized on positively charged lipid bilayers, clusters of HMM‐GFP were readily formed. Time‐lapse observation revealed that the clusters grew unidirectionally. When we used a mixture of actin filaments and copolymers of actin and acto‐S1dC, a chimeric protein of actin and the myosin motor domain, HMM‐GFP preferentially formed clusters along the copolymers. We thus suggest that binding of myosin motors carrying ADP and Pi induces unidirectional conformational changes in actin filaments and allosterically recruits more myosin binding. In contrast, when actin filaments and copolymers were anchored to glass substrate via stable biotin‐avidin linkage, higher concentrations of HMM‐GFP were required to form clusters than on the lipid bilayer. Moreover, actin filaments and copolymers were not discriminated regarding preferential cluster formation. This is presumably because the myosin‐induced cooperative conformational changes in actin filaments involve changes in the helical twist. Consistent with this, cofilin clusters, which supertwist the helix, were readily formed along loosely immobilized actin filaments, but not along those anchored via biotin‐avidin linkage.