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Updated: Aug 20, 2026

Genetic and Biochemical Approaches for In Vivo and In Vitro Assessment of Protein Oligomerization: The Ryanodine Receptor Case Study
Published on: July 27, 2016
Interaction of FKBP12.6 with the cardiac ryanodine receptor C-terminal domain
Spyros Zissimopoulos1, F Anthony Lai
1Wales Heart Research Institute, Department of Cardiology, University of Wales College of Medicine, Cardiff CF14 4XN, UK.
Insights
Researchers identified a new binding site for FKBP12.6 on the RyR2 C-terminal domain. This discovery advances understanding of the ryanodine receptor-FKBP interaction in cardiac function and disease.
Area of Science:
- Cardiovascular Biology
- Molecular Physiology
- Ion Channel Research
Background:
- The ryanodine receptor (RyR) complex is crucial for muscle excitation-contraction coupling.
- FK506-binding protein (FKBP) interaction modulates RyR activity, and its disruption is linked to heart failure.
- The precise FKBP-binding site on RyR, particularly FKBP12.6 on RyR2, remains poorly defined.
Purpose of the Study:
- To identify and characterize the FKBP12.6-binding site on the human RyR2.
- To investigate the role of different RyR2 domains in FKBP12.6 interaction.
Main Methods:
- Competition binding assays using RyR2 C-terminal fragments.
- Expression of RyR2 C-terminal constructs in mammalian cells.
- Rapamycin-sensitive binding assays to differentiate FKBP12.6 and FKBP12 interactions.
Main Results:
- RyR2 C-terminal fragments competed with FKBP12.6 binding to native RyR2.
- A large RyR2 C-terminal construct showed specific, rapamycin-sensitive binding to FKBP12.6.
- Evidence suggests potential involvement of the RyR2 N-terminal domain, but not the central domain.
Conclusions:
- A novel FKBP12.6-binding site is identified on the human RyR2 C-terminal domain, near the channel pore.
- This C-terminal site is sterically positioned to modulate RyR2 channel activity.
- Findings offer new insights into RyR-FKBP interactions in cardiac physiology and pathology.
Abstract:
The ryanodine receptor-calcium release channel complex (RyR) plays a pivotal role in excitation-contraction coupling in skeletal and cardiac muscle. RyR channel activity is modulated by interaction with FK506-binding protein (FKBP), and disruption of the RyR-FKBP association has been implicated in cardiomyopathy, cardiac hypertrophy, and heart failure. Evidence for an interaction between RyR and FKBP is well documented, both in skeletal muscle (RyR1-FKBP12) and in cardiac muscle (RyR2-FKBP12.6), however definition of the FKBP-binding site remains elusive. Early reports proposed interaction of a short RyR central domain with FKBP12/12.6, however this site has been questioned, and recently an alternative FKBP12.6 interaction site has been identified within the N-terminal half of RyR2. In this study, we report evidence for the human RyR2 C-terminal domain as a novel FKBP12.6-binding site. Using competition binding assays, we find that short C-terminal RyR2 fragments can displace bound FKBP12.6 from the native RyR2, although they are unable to exclusively support interaction with FKBP12.6. However, expression of a large RyR2 C-terminal construct in mammalian cells encompassing the pore-forming transmembrane domains exhibits rapamycin-sensitive binding specifically to FKBP12.6 but not to FKBP12. We also obtained some evidence for involvement of the RyR2 N-terminal, but not the central domain, in FKBP12.6 interaction. Our studies suggest that a novel interaction site for FKBP12.6 may be present at the RyR2 C terminus, proximal to the channel pore, a sterically appropriate location that would enable this protein to play a central role in the modulation of this critical ion channel.
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