{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Clobes AM"],"funding":["NIGMS NIH HHS"],"pagination":["143-52"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC4096411"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["35(2)"],"pubmed_abstract":["Myosin's actin-binding loop (loop 2) carries a charge opposite to that of its binding site on actin and is thought to play an important role in ionic interactions between the two molecules during the initial binding step. However, no subsequent role has been identified for loop 2 in actin-myosin binding. We used an optical trap to measure bond formation and bond rupture between actin and rigor heavy meromyosin when loaded perpendicular to the filament axis. We studied HMM with intact or proteolytically cleaved loop 2 at low and physiologic ionic strength. Here we show that the presence of intact loop 2 allows actomyosin bonds to form quickly and that they do so in a short-lived bound state. Increasing tensile load causes the transition to a long-lived state-the distinguishing behavior of a"],"journal":["Journal of muscle research and cell motility"],"pubmed_title":["Loop 2 of myosin is a force-dependent inhibitor of the rigor bond."],"pmcid":["PMC4096411"],"funding_grant_id":["T32GM080186","T32 GM080186"],"pubmed_authors":["Clobes AM","Guilford WH"],"additional_accession":[]},"is_claimable":false,"name":"Loop 2 of myosin is a force-dependent inhibitor of the rigor bond.","description":"Myosin's actin-binding loop (loop 2) carries a charge opposite to that of its binding site on actin and is thought to play an important role in ionic interactions between the two molecules during the initial binding step. However, no subsequent role has been identified for loop 2 in actin-myosin binding. We used an optical trap to measure bond formation and bond rupture between actin and rigor heavy meromyosin when loaded perpendicular to the filament axis. We studied HMM with intact or proteolytically cleaved loop 2 at low and physiologic ionic strength. Here we show that the presence of intact loop 2 allows actomyosin bonds to form quickly and that they do so in a short-lived bound state. Increasing tensile load causes the transition to a long-lived state-the distinguishing behavior of a","dates":{"release":"2014-01-01T00:00:00Z","publication":"2014 Apr","modification":"2025-05-29T20:19:38.207Z","creation":"2025-05-29T20:19:38.207Z"},"accession":"S-EPMC4096411","cross_references":{"pubmed":["24500136"],"doi":["10.1007/s10974-014-9375-z"]}}