Key result
BDM enhances myosin-actin binding rigidity and increases effective myosin heads in congenital myopathy models.
Why the study?
The molecular mechanisms of myosin inhibition by 2,3-butanedione-monoxime (BDM) in skeletal muscle were unstudied, limiting assessment of its potential to treat congenital myopathies.
Does 2,3-butanedione-monoxime (BDM) improve myosin-actin interaction in skeletal muscle fiber models of congenital myopathy?
Does 2,3-butanedione-monoxime (BDM) improve myosin-actin interaction in skeletal muscle fiber models of congenital myopathy?
BDM partially inhibits the pathological effects of the R90P tropomyosin mutation in skeletal muscle models, suggesting potential therapeutic value for congenital myopathies.
BDM may mitigate R90P effects in animal fiber models; leaves open therapeutic translation to congenital myopathies.
Congenital myopathies are a heterogeneous group of human skeletal muscle disorders characterized by muscle hypotonia and weakness. Myopathies have a wide range of clinical phenotypes, which makes it extremely difficult to develop approaches to their treatment. There are several pharmacological agents in clinical use or under clinical investigation for the treatment of cardiomyopathies whose mechanism of action can be used to treat congenital myopathies as well. One such agent is 2,3-butanedione-monoxime (BDM), a noncompetitive inhibitor of myosin ATPase activity used to suppress acute myocardial injury. The molecular mechanisms of inhibition of myosin by BDM in skeletal muscle have not been studied, therefore the aim of this work was to estimate the effect of BDM on the interaction of myosin with actin in the modeling of several ATPase stages in skeletal muscle fiber, in order to assess the prospects for the use of BDM for the treatment of congenital myopathies. We found that BDM enhances the rigidity of myosin binding to actin when modeling weak binding forms of these muscle proteins, which can slow down the transition of actomyosin from the AM ∙ ADP ∙ Pi to the AM ∙ ADP state and is one of the reasons for the decrease in myosin ATPase activity in the presence of BDM. When modeling successive stages of the ATPase cycle using ADP, AMPPNP, ATPγS, and ATP, the myosin heads gradually switch to a state of weak interaction with actin. In the presence of the regulatory proteins tropomyosin and troponin in the muscle fiber, BDM does not affect the formation of a weak form of actomyosin binding, but increases the number of myosin heads essential for force generation. BDM can be used to increase the efficiency of myosin conformational rearrangements in the presence of tropomyosin with the R90P mutation associated with congenital myopathy, since this reagent increases the number of myosin heads in the muscle fiber capable of effective conformational rearrangements in the ATPase cycle and partially inhibits the pathological effects of the mutation.
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Andreeva et al. (2023) studied Congenital myopathy. 2,3-butanedione-monoxime (BDM) was evaluated on Interaction of myosin with actin in the modeling of several ATPase stages in skeletal muscle fiber. 2,3-butanedione-monoxime (BDM) enhances the rigidity of myosin binding to actin and increases the number of myosin heads capable of effective conformational rearrangements in congenital myopathy models.
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