Ryanodine receptors: structure and function.
暂无分享,去创建一个
[1] I. Serysheva,et al. Ryanodine Receptor Structure: Progress and Challenges* , 2009, Journal of Biological Chemistry.
[2] Apo and InsP3-Bound Crystal Structures of the Ligand-Binding Domain of an InsP3 Receptor , 2011 .
[3] M. Endo,et al. Enhancing effect of calmodulin on Ca(2+)‐induced Ca2+ release in the sarcoplasmic reticulum of rabbit skeletal muscle fibres. , 1995, The Journal of physiology.
[4] F. V. Petegem,et al. The structural biology of ryanodine receptors , 2011, Science China Life Sciences.
[5] H. T. ter Keurs,et al. Ser-2030, but not Ser-2808, is the major phosphorylation site in cardiac ryanodine receptors responding to protein kinase A activation upon beta-adrenergic stimulation in normal and failing hearts. , 2006, The Biochemical journal.
[6] T. Wagenknecht,et al. Dynamic, inter-subunit interactions between the N-terminal and central mutation regions of cardiac ryanodine receptor , 2010, Journal of Cell Science.
[7] A. Fabiato,et al. Calcium-induced release of calcium from the cardiac sarcoplasmic reticulum , 1983 .
[8] K. Otsu,et al. Identification of a mutation in porcine ryanodine receptor associated with malignant hyperthermia. , 1991, Science.
[9] Paul D Allen,et al. Structural characterization of the RyR1-FKBP12 interaction. , 2006, Journal of molecular biology.
[10] C. Valdivia,et al. Calcium-dependent block of ryanodine receptor channel of swine skeletal muscle by direct binding of calmodulin. , 1994, Cell calcium.
[11] F. Koniuszy,et al. Plant insecticides; ryanodine, a new alkaloid from Ryania speciosa Vahl. , 1948, Journal of the American Chemical Society.
[12] B. Xiao,et al. Enhanced Basal Activity of a Cardiac Ca2+ Release Channel (Ryanodine Receptor) Mutant Associated With Ventricular Tachycardia and Sudden Death , 2002, Circulation research.
[13] B. Prosser,et al. S100A1 and calmodulin regulation of ryanodine receptor in striated muscle. , 2011, Cell calcium.
[14] C. H. George,et al. Ryanodine Receptor Mutations Associated With Stress-Induced Ventricular Tachycardia Mediate Increased Calcium Release in Stimulated Cardiomyocytes , 2003, Circulation research.
[15] M. Phillips,et al. A mutation in the human ryanodine receptor gene associated with central core disease , 1993, Nature Genetics.
[16] David J Weber,et al. S100A1 and Calmodulin Compete for the Same Binding Site on Ryanodine Receptor* , 2008, Journal of Biological Chemistry.
[17] Y. Shamoo,et al. Complex of calmodulin with a ryanodine receptor target reveals a novel, flexible binding mode. , 2006, Structure.
[18] R. Haworth,et al. Abnormal Ca2+ Release, but Normal Ryanodine Receptors, in Canine and Human Heart Failure , 2002, Circulation research.
[19] B. Britt,et al. A substitution of cysteine for arginine 614 in the ryanodine receptor is potentially causative of human malignant hyperthermia. , 1991, Genomics.
[20] Huihui Kong,et al. Reduced Threshold for Luminal Ca2+ Activation of RyR1 Underlies a Causal Mechanism of Porcine Malignant Hyperthermia* , 2008, Journal of Biological Chemistry.
[21] C. Ward,et al. Leaky Ca2+ release channel/ryanodine receptor 2 causes seizures and sudden cardiac death in mice. , 2008, The Journal of clinical investigation.
[22] Stephan E. Lehnart,et al. Ca2+/Calmodulin-Dependent Protein Kinase II Phosphorylation Regulates the Cardiac Ryanodine Receptor , 2004, Circulation research.
[23] P. Allen,et al. Coordinated Movement of Cytoplasmic and Transmembrane Domains of RyR1 upon Gating , 2009, PLoS biology.
[24] Filip Van Petegem,et al. The amino-terminal disease hotspot of ryanodine receptors forms a cytoplasmic vestibule , 2010, Nature.
[25] N. Sambuughin,et al. Exertional rhabdomyolysis and malignant hyperthermia in a patient with ryanodine receptor type 1 gene, L-type calcium channel alpha-1 subunit gene, and calsequestrin-1 gene polymorphisms. , 2010, Anesthesiology.
[26] J. Nakai,et al. Primary structure and functional expression from cDN A of the cardiac ryanodine receptor/calcium release channel , 1990, FEBS letters.
[27] J. Nakai,et al. Primary structure and distribution of a novel ryanodine receptor/calcium release channel from rabbit brain , 1992, FEBS letters.
[28] L. Blayney,et al. Physical coupling between ryanodine receptor-calcium release channels. , 2005, Journal of molecular biology.
[29] S. Priori,et al. FKBP12.6 Deficiency and Defective Calcium Release Channel (Ryanodine Receptor) Function Linked to Exercise-Induced Sudden Cardiac Death , 2003, Cell.
[30] L. Xu,et al. Calmodulin activation and inhibition of skeletal muscle Ca2+ release channel (ryanodine receptor). , 1995, Biophysical journal.
[31] David D. Thomas,et al. FRET-based mapping of calmodulin bound to the RyR1 Ca2+ release channel , 2009, Proceedings of the National Academy of Sciences.
[32] K. Fogarty,et al. Type 1 ryanodine receptor knock-in mutation causing central core disease of skeletal muscle also displays a neuronal phenotype , 2011, Proceedings of the National Academy of Sciences.
[33] D. Maclennan,et al. Mechanistic models for muscle diseases and disorders originating in the sarcoplasmic reticulum. , 2011, Biochimica et biophysica acta.
[34] R. D. Mitchell,et al. Spontaneous calcium release from sarcoplasmic reticulum. General description and effects of calcium. , 1983, The Journal of biological chemistry.
[35] M. Phillips,et al. Molecular cloning of cDNA encoding human and rabbit forms of the Ca2+ release channel (ryanodine receptor) of skeletal muscle sarcoplasmic reticulum. , 1990, The Journal of biological chemistry.
[36] F. Wappler,et al. Dantrolene – A review of its pharmacology, therapeutic use and new developments , 2004, Anaesthesia.
[37] M. Casarotto,et al. Cyclization of the Intrinsically Disordered α1S Dihydropyridine Receptor II-III Loop Enhances Secondary Structure and in Vitro Function* , 2011, The Journal of Biological Chemistry.
[38] F. van Petegem,et al. Disease mutations in the ryanodine receptor central region: crystal structures of a phosphorylation hot spot domain. , 2012, Structure.
[39] S. Priori,et al. Mutations in the Cardiac Ryanodine Receptor Gene (hRyR2) Underlie Catecholaminergic Polymorphic Ventricular Tachycardia , 2001, Circulation.
[40] B. Xiao,et al. Localization of the 12.6-kDa FK506-binding Protein (FKBP12.6) Binding Site to the NH2-terminal Domain of the Cardiac Ca2+ Release Channel (Ryanodine Receptor)* , 2003, The Journal of Biological Chemistry.
[41] T. Wagenknecht,et al. Three-dimensional Structure of Ryanodine Receptor Isoform Three in Two Conformational States as Visualized by Cryo-electron Microscopy* , 2000, The Journal of Biological Chemistry.
[42] D. Bers,et al. Ca2+/Calmodulin–Dependent Protein Kinase Modulates Cardiac Ryanodine Receptor Phosphorylation and Sarcoplasmic Reticulum Ca2+ Leak in Heart Failure , 2005, Circulation research.
[43] M. Ikura,et al. Structural and functional conservation of key domains in InsP3 and ryanodine receptors , 2011, Nature.
[44] T. Wagenknecht,et al. Amino acid residues 4425-4621 localized on the three-dimensional structure of the skeletal muscle ryanodine receptor. , 2000, Biophysical journal.
[45] D. Maclennan,et al. Identification of calmodulin-, Ca(2+)-, and ruthenium red-binding domains in the Ca2+ release channel (ryanodine receptor) of rabbit skeletal muscle sarcoplasmic reticulum. , 1994, The Journal of biological chemistry.
[46] G. Meissner,et al. Ryanodine activation and inhibition of the Ca2+ release channel of sarcoplasmic reticulum. , 1986, The Journal of biological chemistry.
[47] F. van Petegem,et al. The deletion of exon 3 in the cardiac ryanodine receptor is rescued by β strand switching. , 2011, Structure.
[48] K. Beam,et al. Restoration of excitation—contraction coupling and slow calcium current in dysgenic muscle by dihydropyridine receptor complementary DNA , 1988, Nature.
[49] G. Meissner,et al. Kinetics of rapid Ca2+ release by sarcoplasmic reticulum. Effects of Ca2+, Mg2+, and adenine nucleotides. , 1986, Biochemistry.
[50] B. Adams,et al. Regions of the skeletal muscle dihydropyridine receptor critical for excitation–contraction coupling , 1990, Nature.
[51] K. Campbell,et al. Structural evidence for direct interaction between the molecular components of the transverse tubule/sarcoplasmic reticulum junction in skeletal muscle , 1988, The Journal of cell biology.
[52] F. van Petegem,et al. Crystal structures of the N-terminal domains of cardiac and skeletal muscle ryanodine receptors: insights into disease mutations. , 2009, Structure.
[53] D. Jiang,et al. Loss of luminal Ca2+ activation in the cardiac ryanodine receptor is associated with ventricular fibrillation and sudden death , 2007, Proceedings of the National Academy of Sciences.
[54] S. Fleischer,et al. Purification of the ryanodine receptor and identity with feet structures of junctional terminal cisternae of sarcoplasmic reticulum from fast skeletal muscle. , 1987, The Journal of biological chemistry.
[55] David D. Thomas,et al. Mapping the Ryanodine Receptor FK506-binding Protein Subunit Using Fluorescence Resonance Energy Transfer* , 2010, The Journal of Biological Chemistry.
[56] P. Junankar,et al. Subconductance states in single-channel activity of skeletal muscle ryanodine receptors after removal of FKBP12. , 1997, Biophysical journal.
[57] Huihui Kong,et al. Enhanced Store Overload–Induced Ca2+ Release and Channel Sensitivity to Luminal Ca2+ Activation Are Common Defects of RyR2 Mutations Linked to Ventricular Tachycardia and Sudden Death , 2005, Circulation research.
[58] Harold P. Erickson,et al. Purification and reconstitution of the calcium release channel from skeletal muscle , 1988, Nature.
[59] T. Shiomi,et al. Ryanodine receptor oxidation causes intracellular calcium leak and muscle weakness in aging. , 2011, Cell metabolism.
[60] Wah Chiu,et al. The pore structure of the closed RyR1 channel. , 2005, Structure.
[61] Montserrat Samsó,et al. Apocalmodulin and Ca2+-Calmodulin Bind to Neighboring Locations on the Ryanodine Receptor* , 2002, The Journal of Biological Chemistry.
[62] D. Bers. Macromolecular complexes regulating cardiac ryanodine receptor function. , 2004, Journal of molecular and cellular cardiology.
[63] A. Lemainque,et al. A recessive form of central core disease, transiently presenting as multi‐minicore disease, is associated with a homozygous mutation in the ryanodine receptor type 1 gene , 2002, Annals of neurology.
[64] Zhe Lu,et al. Apo and InsP3-bound crystal structures of the ligand-binding domain of an InsP3 receptor , 2011, Nature Structural &Molecular Biology.
[65] Montserrat Samsó,et al. Internal structure and visualization of transmembrane domains of the RyR1 calcium release channel by cryo-EM , 2005, Nature Structural &Molecular Biology.
[66] C. Doriguzzi,et al. Mutations in the ryanodine receptor gene in central core disease and malignant hyperthermia , 1993, Nature Genetics.
[67] M. Endo,et al. Calcium Induced Release of Calcium from the Sarcoplasmic Reticulum of Skinned Skeletal Muscle Fibres , 1970, Nature.
[68] D. Burkhoff,et al. PKA Phosphorylation Dissociates FKBP12.6 from the Calcium Release Channel (Ryanodine Receptor) Defective Regulation in Failing Hearts , 2000, Cell.
[69] H. Takeshima,et al. Primary structure and expression from complementary DNA of skeletal muscle ryanodine receptor , 1989, Nature.
[70] T. Wagenknecht,et al. Cryoelectron Microscopy and Image Analysis of the Cardiac Ryanodine Receptor* , 1998, The Journal of Biological Chemistry.
[71] F. Muntoni,et al. Multi-minicore disease and atypical periodic paralysis associated with novel mutations in the skeletal muscle ryanodine receptor (RYR1) gene , 2010, Neuromuscular Disorders.
[72] Heping Cheng,et al. RyR2 mutations linked to ventricular tachycardia and sudden death reduce the threshold for store-overload-induced Ca2+ release (SOICR). , 2004, Proceedings of the National Academy of Sciences of the United States of America.
[73] H. Willard,et al. Molecular cloning of cDNA encoding the Ca2+ release channel (ryanodine receptor) of rabbit cardiac muscle sarcoplasmic reticulum. , 1990, The Journal of biological chemistry.
[74] A. Dulhunty,et al. Ca2+ signaling in striated muscle: the elusive roles of triadin, junctin, and calsequestrin , 2009, European Biophysics Journal.
[75] S. Hamilton,et al. Regulation of ryanodine receptors by FK506 binding proteins. , 2004, Trends in cardiovascular medicine.
[76] R. Robinson,et al. Mutations in RYR1 in malignant hyperthermia and central core disease , 2006, Human mutation.
[77] C. Louis,et al. Dantrolene Inhibition of Ryanodine Receptor Ca2+Release Channels , 2001, The Journal of Biological Chemistry.
[78] E. Ríos,et al. Involvement of dihydropyridine receptors in excitation–contraction coupling in skeletal muscle , 1987, Nature.
[79] Clara Franzini-Armstrong,et al. STUDIES OF THE TRIAD I. Structure of the Junction in Frog Twitch Fibers , 1970 .
[80] A. Marks,et al. Ryanodine receptor channelopathies , 2010, Pflügers Archiv - European Journal of Physiology.
[81] S. Treves,et al. Calcium dependent activation of skeletal muscle Ca2+ release channel (ryanodine receptor) by calmodulin. , 1995, Biochemical and biophysical research communications.
[82] Xinghua Guo,et al. Topology of the Ca2+ release channel of skeletal muscle sarcoplasmic reticulum (RyR1) , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[83] C Franzini-Armstrong,et al. STUDIES OF THE TRIAD , 1973, The Journal of cell biology.
[84] S. Marx,et al. Coupled gating between individual skeletal muscle Ca2+ release channels (ryanodine receptors) , 1998, Science.
[85] T. Wagenknecht,et al. Localization of an NH2-terminal Disease-causing Mutation Hot Spot to the “Clamp” Region in the Three-dimensional Structure of the Cardiac Ryanodine Receptor* , 2007, Journal of Biological Chemistry.
[86] M. Baker,et al. Subnanometer-resolution electron cryomicroscopy-based domain models for the cytoplasmic region of skeletal muscle RyR channel , 2008, Proceedings of the National Academy of Sciences.
[87] Silvia G Priori,et al. Inherited dysfunction of sarcoplasmic reticulum Ca2+ handling and arrhythmogenesis. , 2011, Circulation research.
[88] S. Muldoon,et al. The Relationship Between Exertional Heat Illness, Exertional Rhabdomyolysis, and Malignant Hyperthermia , 2009, Anesthesia and analgesia.
[89] M. Yano,et al. Defective Regulation of Interdomain Interactions Within the Ryanodine Receptor Plays a Key Role in the Pathogenesis of Heart Failure , 2005, Circulation.
[90] F. A. Lai,et al. Intrinsic lattice formation by the ryanodine receptor calcium-release channel , 2000, Nature Cell Biology.
[91] S. Grinstein,et al. Caffeine and Halothane Sensitivity of Intracellular Ca2+ Release Is Altered by 15 Calcium Release Channel (Ryanodine Receptor) Mutations Associated with Malignant Hyperthermia and/or Central Core Disease* , 1997, The Journal of Biological Chemistry.
[92] Stephan E Lehnart,et al. Modulation of the ryanodine receptor and intracellular calcium. , 2007, Annual review of biochemistry.
[93] Dimitra K. Georgiou,et al. Ryanodine receptors: structure, expression, molecular details, and function in calcium release. , 2010, Cold Spring Harbor perspectives in biology.
[94] P. Williams,et al. Identification of a Dantrolene-binding Sequence on the Skeletal Muscle Ryanodine Receptor* , 2002, The Journal of Biological Chemistry.
[95] M. Ikura,et al. Crystal structure of type I ryanodine receptor amino-terminal β-trefoil domain reveals a disease-associated mutation “hot spot” loop , 2009, Proceedings of the National Academy of Sciences.
[96] R. Lovell,et al. ANÆSTHETIC DEATHS IN A FAMILY , 1960 .
[97] A. Wilde,et al. Expanding Spectrum of Human RYR2-Related Disease: New Electrocardiographic, Structural, and Genetic Features , 2007, Circulation.
[98] Wah Chiu,et al. Flexible architecture of IP3R1 by Cryo-EM. , 2011, Structure.
[99] M. A. Shea,et al. Lobe-dependent Regulation of Ryanodine Receptor Type 1 by Calmodulin* , 2002, The Journal of Biological Chemistry.