Kuehn Michel N, Engels Nichlas M, Nissen Devin L, Freundt Johanna K, Ma Weikang, Irving Thomas C, Linke Wolfgang A, Hessel Anthony L
Institute of Physiology II, University of Muenster; Muenster, Germany.
Department of Cellular and Molecular Medicine, University of Arizona; Tucson, AZ, USA.
bioRxiv. 2024 Dec 3:2024.11.29.626031. doi: 10.1101/2024.11.29.626031.
The first-in-its-class cardiac drug mavacamten reduces the proportion of so-called ON-state myosin heads in relaxed sarcomeres, altering contraction performance. However, mavacamten is not completely specific to cardiac myosin and can also affect skeletal muscle myosin, an important consideration since mavacamten is administered orally and so will also be present in skeletal tissue. Here, we studied the effect of mavacamten on skeletal muscle structure using small-angle X-ray diffraction. Mavacamten treatment reduced the proportion of ON myosin heads but did not eliminate the molecular underpinnings of length-dependent activation, demonstrating similar effects to those observed in cardiac muscle. These findings provide valuable insights for the potential use of mavacamten as a tool to study muscle contraction across striated muscle.
首款同类心脏药物mavacamten可降低松弛肌节中所谓处于“开启”状态的肌球蛋白头部比例,从而改变收缩性能。然而,mavacamten并非完全特异性作用于心肌肌球蛋白,它也会影响骨骼肌肌球蛋白,这是一个重要的考量因素,因为mavacamten是口服给药,所以也会存在于骨骼组织中。在此,我们使用小角X射线衍射研究了mavacamten对骨骼肌结构的影响。mavacamten治疗降低了处于“开启”状态的肌球蛋白头部比例,但并未消除长度依赖性激活的分子基础,这表明其作用效果与在心肌中观察到的相似。这些发现为mavacamten作为研究横纹肌收缩的工具的潜在用途提供了有价值的见解。