TY - JOUR U1 - Zeitschriftenartikel, wissenschaftlich - begutachtet (reviewed) A1 - Ewert, Wiebke A1 - Franz, Peter A1 - Tsiavaliaris, Georgios A1 - Preller, Matthias T1 - Structural and Computational Insights into a Blebbistatin-Bound Myosin•ADP Complex with Characteristics of an ADP-Release Conformation along the Two-Step Myosin Power Stoke JF - International Journal of Molecular Sciences N2 - The motor protein myosin drives a wide range of cellular and muscular functions by generating directed movement and force, fueled through adenosine triphosphate (ATP) hydrolysis. Release of the hydrolysis product adenosine diphosphate (ADP) is a fundamental and regulatory process during force production. However, details about the molecular mechanism accompanying ADP release are scarce due to the lack of representative structures. Here we solved a novel blebbistatin-bound myosin conformation with critical structural elements in positions between the myosin pre-power stroke and rigor states. ADP in this structure is repositioned towards the surface by the phosphate-sensing P-loop, and stabilized in a partially unbound conformation via a salt-bridge between Arg131 and Glu187. A 5 Å rotation separates the mechanical converter in this conformation from the rigor position. The crystallized myosin structure thus resembles a conformation towards the end of the two-step power stroke, associated with ADP release. Computationally reconstructing ADP release from myosin by means of molecular dynamics simulations further supported the existence of an equivalent conformation along the power stroke that shows the same major characteristics in the myosin motor domain as the resolved blebbistatin-bound myosin-II·ADP crystal structure, and identified a communication hub centered on Arg232 that mediates chemomechanical energy transduction. KW - molecular dynamics simulations KW - cytoskeleton KW - ADP release KW - myosin KW - structural biology KW - force generation KW - molecular motor KW - blebbistatin UN - https://nbn-resolving.org/urn:nbn:de:hbz:1044-opus-50854 SN - 1422-0067 SS - 1422-0067 U6 - https://doi.org/10.3390/ijms21197417 DO - https://doi.org/10.3390/ijms21197417 PM - 33049993 VL - 21 IS - 19 SP - 24 S1 - 24 PB - MDPI CY - Basel ER -