8RRV
Structure of RyR1 in detergent in close state in complex with FKBP and Nb9657.
This is a non-PDB format compatible entry.
Summary for 8RRV
Entry DOI | 10.2210/pdb8rrv/pdb |
EMDB information | 19466 |
Descriptor | Ryanodine receptor 1, Peptidyl-prolyl cis-trans isomerase FKBP1B, nanobody9657, ... (4 entities in total) |
Functional Keywords | ion channel, ca2+, tetramer, transport protein |
Biological source | Vicugna pacos More |
Total number of polymer chains | 12 |
Total formula weight | 2371011.34 |
Authors | Li, C.,Efremov, R.G. (deposition date: 2024-01-23, release date: 2024-10-09, Last modification date: 2024-11-13) |
Primary citation | Li, C.,Willegems, K.,Uchanski, T.,Pardon, E.,Steyaert, J.,Efremov, R.G. Rapid small-scale nanobody-assisted purification of ryanodine receptors for cryo-EM. J.Biol.Chem., 300:107734-107734, 2024 Cited by PubMed Abstract: Ryanodine receptors (RyRs) are large Ca release channels residing in the endoplasmic or sarcoplasmic reticulum membrane. Three isoforms of RyRs have been identified in mammals, the disfunction of which has been associated with a series of life-threatening diseases. The need for large amounts of native tissue or eukaryotic cell cultures limits advances in structural studies of RyRs. Here, we report a method that utilizes nanobodies to purify RyRs from only 5 mg of total protein. The purification process, from isolated membranes to cryo-EM grade protein, is achieved within 4 h on the bench, yielding protein usable for cryo-EM analysis. This is demonstrated by solving the structures of rabbit RyR1, solubilized in detergent, reconstituted into lipid nanodiscs or liposomes, and bovine RyR2 reconstituted in nanodisc, and mouse RyR2 in detergent. The reported method facilitates structural studies of RyRs directed toward drug development and is useful in cases where the amount of starting material is limited. PubMed: 39233227DOI: 10.1016/j.jbc.2024.107734 PDB entries with the same primary citation |
Experimental method | ELECTRON MICROSCOPY (3.2 Å) |
Structure validation
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