abstracts
Calcium ions play crucial roles in our bodies, acting as second messengers in multiple signaling pathways. The resting calcium levels in the cytosol are very low, but can increase rapidly and transiently by influx from the extracellular space, or by release from intracellular stores. The Endoplasmic and Sarcoplasmic Reticulum (ER/SR) form major intracellular calcium stores. The `Ryanodine Receptor' (RyR) is a protein that dictates calcium release from the ER/SR. It forms a huge ion channel with a molecular weight exceeding 2 MegaDalton. RyRs are expressed in multiple cell types, but are particularly abundant in cardiac and skeletal muscle, where they are directly involved in excitation-contraction coupling. Three RyR isoforms exist in mammalian species (RyR1, RyR2, RyR3). Mutations in RyR1 and RyR2 have been linked to a number of devastating genetic disorders, including stress-induced cardiac arrhythmias (CPVT), malignant hyperthermia, and central core disease. In the past 5 years we have been solving crystal structures of several RyR domains. Cryo-electron microscopy structures have helped us to build pseudo-atomic models, allowing us to locate these domains in full-length RyRs. Over 80 disease mutations are scattered throughout the structures. The bulk of these affect domain-domain interactions. By comparing the RyR in the open and closed state, we find that some of these interactions are labile: they are disrupted during channel opening. Many disease mutations weaken these interactions, leading to facilitated channel opening, resulting in premature or prolonged release of calcium. In addition, many other disease mutations affect the same labile interactions allosterically. Stabilizing the closed-state domain-domain interactions may therefore be of therapeutic value.
abstracts
The ryanodine receptor is the largest ion channel known. It is responsible for the release of calcium ions from the intracellular stores of the sarcoplasmic/endoplasmic reticulum. The release of calcium signals for a wide assortment of cellular processes, most importantly, muscle contraction in skeletal and cardiac tissue. Only two regions of this receptor have been described by high-resolution crystal structures. In addition these two domains have been docked into low-resolution cryo-EM structures. Here, I will present a x-ray crystal structure of a novel domain from the ryanodine receptor of both skeletal and cardiac isoforms. Stability of the wild-type versus those of mutants will be discussed as well as the implications of the structure of a mutant linked to cardiac hypertrophy and a loss of function phenotype. The docked location of the domain within the whole channel may suggest its functional properties.