Validation of cryo-EM structure of IP₃R1 channel. 2013

Stephen C Murray, and John Flanagan, and Olga B Popova, and Wah Chiu, and Steven J Ludtke, and Irina I Serysheva
Graduate Program in Structural and Computational Biology and Molecular Biophysics, Baylor College of Medicine, One Baylor Plaza, Houston, TX 77030, USA.

About a decade ago, three electron cryomicroscopy (cryo-EM) single-particle reconstructions of IP3R1 were reported at low resolution. It was disturbing that these structures bore little similarity to one another, even at the level of quaternary structure. Recently, we published an improved structure of IP3R1 at ∼1 nm resolution. However, this structure did not bear any resemblance to any of the three previously published structures, leading to the question of why the structure should be considered more reliable than the original three. Here, we apply several methods, including class-average/map comparisons, tilt-pair validation, and use of multiple refinement software packages, to give strong evidence for the reliability of our recent structure. The map resolution and feature resolvability are assessed with the gold standard criterion. This approach is generally applicable to assessing the validity of cryo-EM maps of other molecular machines.

UI MeSH Term Description Entries
D011487 Protein Conformation The characteristic 3-dimensional shape of a protein, including the secondary, supersecondary (motifs), tertiary (domains) and quaternary structure of the peptide chain. PROTEIN STRUCTURE, QUATERNARY describes the conformation assumed by multimeric proteins (aggregates of more than one polypeptide chain). Conformation, Protein,Conformations, Protein,Protein Conformations
D053496 Inositol 1,4,5-Trisphosphate Receptors Intracellular receptors that bind to INOSITOL 1,4,5-TRISPHOSPHATE and play an important role in its intracellular signaling. Inositol 1,4,5-trisphosphate receptors are calcium channels that release CALCIUM in response to increased levels of inositol 1,4,5-trisphosphate in the CYTOPLASM. Inositol 1,4,5-Triphosphate Receptor,Inositol 1,4,5-Triphosphate Receptors,Inositol 1,4,5-Trisphosphate Receptor,1,4,5-INTP Receptor,INSP3 Receptor,INSP3 Receptor Type 1,INSP3 Receptor Type 2,INSP3 Receptor Type 3,IP3 Receptor,Inositol 1,4,5-trisphosphate Receptor Subtype 3,Inositol 1,4,5-trisphosphate Receptor Type 1,Inositol 1,4,5-trisphosphate Receptor Type 2,Inositol 1,4,5-trisphosphate Receptor Type 3,Inositol Triphosphate Receptor,Inositol-1,4,5-Triphosphate Receptor,Receptor, Inositol-1,4,5-triphosphate,Type 1 Inositol 1,4,5-trisphosphate Receptor,Type 3 Inositol 1,4,5-trisphosphate Receptor,Receptor, INSP3,Receptor, IP3,Receptor, Inositol Triphosphate,Triphosphate Receptor, Inositol
D018360 Crystallography, X-Ray The study of crystal structure using X-RAY DIFFRACTION techniques. (McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed) X-Ray Crystallography,Crystallography, X Ray,Crystallography, Xray,X Ray Crystallography,Xray Crystallography,Crystallographies, X Ray,X Ray Crystallographies
D020285 Cryoelectron Microscopy Electron microscopy involving rapid freezing of the samples. The imaging of frozen-hydrated molecules and organelles permits the best possible resolution closest to the living state, free of chemical fixatives or stains. Electron Cryomicroscopy,Cryo-electron Microscopy,Cryo electron Microscopy,Cryo-electron Microscopies,Cryoelectron Microscopies,Cryomicroscopies, Electron,Cryomicroscopy, Electron,Electron Cryomicroscopies,Microscopies, Cryo-electron,Microscopies, Cryoelectron,Microscopy, Cryo-electron,Microscopy, Cryoelectron

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