Three-dimensional Localization of Divergent Region 3 of the Ryanodine Receptor to the Clamp-shaped Structures Adjacent to the FKBP Binding Sites

• Published in: The Journal of biological chemistry Vol. 278; no. 16; pp. 14211 - 14218
• Main Authors: Zhang, Jing, Liu, Zheng, Masumiya, Haruko, Wang, Ruiwu, Jiang, Dawei, Li, Fei, Wagenknecht, Terence, Chen, S. R. Wayne
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 18.04.2003; American Society for Biochemistry and Molecular Biology
• Subjects: Binding Sites; Blotting, Western; Calcium - metabolism; Calcium - pharmacology; Cell Line; Cryoelectron Microscopy; Dose-Response Relationship, Drug; Glutathione Transferase - metabolism; Green Fluorescent Proteins; Humans; Image Processing, Computer-Assisted; Kinetics; Luminescent Proteins - metabolism; Magnesium - pharmacology; Models, Molecular; Muscle, Skeletal - metabolism; Mutation; Protein Binding; Protein Conformation; Protein Folding; Protein Structure, Tertiary; Recombinant Fusion Proteins - metabolism; Ryanodine Receptor Calcium Release Channel - chemistry; Ryanodine Receptor Calcium Release Channel - metabolism; Tacrolimus Binding Proteins - chemistry; Tacrolimus Binding Proteins - metabolism; Tacrolimus-binding protein; Transfection
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.M213164200

Of the three divergent regions of ryanodine receptors (RyRs), divergent region 3 (DR3) is the best studied and is believed to be involved in excitation-contraction coupling as well as in channel regulation by Ca2+ and Mg2+. To gain insight into the structural basis of DR3 function, we have determined the location of DR3 in the three-dimensional structure of RyR2. We inserted green fluorescent protein (GFP) into the middle of the DR3 region after Thr-1874 in the sequence. HEK293 cells expressing this GFP-RyR2 fusion protein, RyR2T1874-GFP, were readily detected by their green fluorescence, indicating proper folding of the inserted GFP. RyR2T1874-GFP was further characterized functionally by assays of Ca2+ release and [3H]ryanodine binding. These analyses revealed that RyR2T1874-GFPfunctions as a caffeine- and ryanodine-sensitive Ca2+release channel and displays Ca2+ dependence and [3H]ryanodine binding properties similar to those of the wild type RyR2. RyR2T1874-GFP was purified from cell lysates in a single step by affinity chromatography using GST-FKBP12.6 as the affinity ligand. The three-dimensional structure of the purified RyR2T1874-GFP was then reconstructed using cryoelectron microscopy and single particle image analysis. Comparison of the three-dimensional reconstructions of wild type RyR2 and RyR2T1874-GFP revealed the location of the inserted GFP, and hence the DR3 region, in one of the characteristic domains of RyR, domain 9, in the clamp-shaped structure adjacent to the FKBP12 and FKBP12.6 binding sites. COOH-terminal truncation analysis demonstrated that a region between 1815 and 1855 near DR3 is essential for GST-FKBP12.6 binding. These results provide a structural basis for the role of the DR3 region in excitation-contraction coupling and in channel regulation.