Ryanodine receptors (RyRs) are Ca 2+ -regulated Ca 2+ channels of 2.2-megadalton in musclesand neurons for calcium signaling. How Ca 2+ regulates ion conduction in the RyR channels remains elusive. We determined a 2.6-Å cryo-EM structure of rabbit skeletal muscle RyR1, and used multiscale dynamics simulations to elucidate cation interactions with RyR1. We investigated 21 potential cation-binding sites that may together rationalize biphasic Ca 2+ response of RyR1. The selectivity filter captures a cation hydration complex by hydrogenbonding with both the inner and outer hydration shells of water molecules. Molecular dynamics simulations suggest that adjacent Ca 2+ ions moving in concert along ionpermeation pathway are separated by at least two cation-binding sites. Our analysis reveals that RyR1 has been evolved to favor its interactions with two hydration shells of cations.Calcium is an important second messenger-an intracellular signaling ion-that regulates a wide variety of cellular activities, such as neurotransmission, secretion, fertilization and cell migration (1). The release of Ca 2+ ions from intracellular stores is predominantly mediated by two related Ca 2+ channel families: the ryanodine receptors (RyRs) (2-5), the largest known ion channels of approximately 2.2-MDa molecular weight, and inositol 1,4,5-trisphosphate receptors (6). RyRs are high-conductance, monovalent-and divalent-conducting channels that are regulated by multiple factors, including Ca 2+ , Mg 2+ , ATP, phosphorylation, redox active species, and by their interactions with regulatory proteins such as FKBPs and calmodulin (5,7). In most tissues, RyR channels are primarily activated by the influx of Ca 2+ via plasma-membrane Ca 2+ channels, resulting in a Ca 2+ -induced rapid release of Ca 2+ from intracellular storage such as endoplasmic reticulum. In mammalian skeletal muscle, RyR1 channels are mechanically activated by direct interaction with voltage-gated L-type Ca 2+ channel dihydropyridine receptor (DHPR or CaV1.1) on the plasma membrane (5,8,9).The general architectures of RyRs have been revealed by cryogenic electron microscopy (cryo-EM) in both basal and activated states (10-18). These structures provided a basis for understanding the regulatory mechanisms of RyRs activation and gating. However, many outstanding questions remain unanswered. How do cations interact with RyR channels? What is the hydration structure of cations permeating through the RyR channels? How do RyRs catalyze the translocation of cations and selectively conduct Ca 2+ over high levels of background monovalent cations? To