The skeletal muscle contraction is determined by cross-bridge formation between the myosin heads and the actin active sites. When the muscle contracts, it shortens, increasing its longitudinal shear elastic modulus (µL). Structurally, skeletal muscle can be considered analogous to the molecular receptors that form receptor–ligand complexes and exhibit specifc ligand-binding dynamics. In this context, this work aims to apply elastography and the ligand-binding framework to approach the possible intrinsic mechanisms behind muscle synergism. Based on the short-range stifness principle and the acoustic–elasticity theory, we defne the coefcient C, which is directly related to the fraction saturation of molecular receptors and links the relative longitudinal deformation of the muscle to its µL. We show that such a coefcient can be obtained directly from µL estimates, thus calculating it for the biceps brachii, brachioradialis, and brachialis muscles during isometric elbow fexion torque (τ) ramps. The resulting C(τ ) curves were analyzed by conventional characterization methods of receptor– ligand systems to study the dynamical behavior of each muscle. The results showed that, depending on muscle, C(τ ) exhibits typical ligand-binding dynamics during joint torque production. Therefore, the above indicates that these diferent behaviors describe the longitudinal shortening pattern of each muscle during load sharing. As a plausible interpretation, we suggested that this could be related to the binding kinetics of the cross-bridges during their synergistic action as torque increases. Likewise, it shows that elastography could be useful to assess contractile processes at diferent scales related to the change in the mechanical properties of skeletal muscle.