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Rapid small-scale nanobody-assisted purification of ryanodine receptors for cryo-EM.
Li, Chenyao; Willegems, Katrien; Uchanski, Tomasz; Pardon, Els; Steyaert, Jan; Efremov, Rouslan G.
Afiliación
  • Li C; Center for Structural Biology, Vlaams Instituut voor Biotechnologie, 1050, Brussels, Belgium; Structural Biology Brussels, Department of Bioengineering Sciences, VUB, 1050, Brussels, Belgium.
  • Willegems K; Center for Structural Biology, Vlaams Instituut voor Biotechnologie, 1050, Brussels, Belgium; Structural Biology Brussels, Department of Bioengineering Sciences, VUB, 1050, Brussels, Belgium.
  • Uchanski T; Center for Structural Biology, Vlaams Instituut voor Biotechnologie, 1050, Brussels, Belgium; Structural Biology Brussels, Department of Bioengineering Sciences, VUB, 1050, Brussels, Belgium.
  • Pardon E; Center for Structural Biology, Vlaams Instituut voor Biotechnologie, 1050, Brussels, Belgium; Structural Biology Brussels, Department of Bioengineering Sciences, VUB, 1050, Brussels, Belgium.
  • Steyaert J; Center for Structural Biology, Vlaams Instituut voor Biotechnologie, 1050, Brussels, Belgium; Structural Biology Brussels, Department of Bioengineering Sciences, VUB, 1050, Brussels, Belgium.
  • Efremov RG; Center for Structural Biology, Vlaams Instituut voor Biotechnologie, 1050, Brussels, Belgium; Structural Biology Brussels, Department of Bioengineering Sciences, VUB, 1050, Brussels, Belgium. Electronic address: rouslan.efremov@vub.be.
J Biol Chem ; : 107734, 2024 Sep 02.
Article en En | MEDLINE | ID: mdl-39233227
ABSTRACT
Ryanodine receptors (RyRs) are large Ca2+ 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 four hours 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.
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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: J Biol Chem Año: 2024 Tipo del documento: Article País de afiliación: Bélgica

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: J Biol Chem Año: 2024 Tipo del documento: Article País de afiliación: Bélgica