The opposite has to be expected, when ON-1910 release channels close again, and the Ca2+ pumping rate exceeds the release rate. 2.3. From Chemical Potentials to Mechanical Force Generation In striated muscle cells like ventricular muscle cells (VMs) or skeletal muscle

fibers (SMFs), force generation as well as shortening is brought about by the cyclic action of cross bridges. It is a known fact that this process is powered by ATP splitting. The underlying mechanism of the energy transduction process, however, is not completely understood. Here, a thermodynamic description of Inhibitors,research,lifescience,medical the cycle is derived using a formalism recently published [1]. It takes into account the basic energetics of enzyme-catalysed reactions, which states that the overall affinity of the catalysed and non-catalysed processes must be equal. For an enzyme-catalysed reaction like: (S = substrate, E = enzyme, ES = enzyme-substrate complex, P = product), this means that Inhibitors,research,lifescience,medical at steady state the sum of the affinities of substrate binding, transition, and product release must yield the affinity of the non-catalysed reaction, which is given by the reaction affinity of all involved

compounds in the bulk solution: (7a) or, after contraction of the first two terms: (7b) yielding, (7c) With K’r = K’B Inhibitors,research,lifescience,medical × K’T × K’R(k’B, k’T, and k’R are equilibrium constants of the binding, transition, and release reaction, respectively, whereas k’r denotes that of the non-catalysed reaction). An analogous reaction sequence is used here to describe the cross-bridge cycle. The following cycle is given in chemical notation, i.e., the charges of involved species are taken into account. The cycle begins with the splitting reaction of the de-energised actomyosin complex (A-M) by MgATP2- in the diffusional space of myofibrils: R1 This Inhibitors,research,lifescience,medical first reaction yields dissociated

actomyosin with MgATP2- bound to myosin (the bold point denotes binding to myosin). Two negative charges develop on the dissociated actin, Inhibitors,research,lifescience,medical which are neutralised by potassium ions, K+, stemming from free MgATP2−, which is now bound to myosin heads. On the dissociated myosin heads, it neutralises both emerging positive charges. This first actomyosin dissociation and binding of MgATP2− to myosin is followed by ATP Sodium butyrate splitting on the myosin heads. This transition reaction is described by R2 It is coupled to the formation of energised myosin (), which is characterised by a tilting of the myosin head from a more bent arms position by an angle of about 60° towards the respective Z disc, so that now the myosin head builds a right angle with the opposing actin filament. contains free energy from reaction R2 as conformational energy. The force generating stroke of the myosin head is triggered by the association reaction to form the energised actomyosin complex (cross-bridge): R3 Because of uncompensated charges, the resulting intermediate in curly brackets lacks firmness.