Ryanodine receptors (RyRs) are Ca2+ release channels in the sarcoplasmic reticulum of skeletal and cardiac muscles and are essential for muscle contraction. Mutations in genes encoding RyRs cause various muscle and arrhythmogenic heart diseases. Although RyR channels are activated by Ca2+, the actual mechanism of Ca2+ binding remains largely unknown. Here, we report the molecular basis of Ca2+ binding to RyRs for channel activation and discuss its implications in disease states. RyR1 and RyR2 carrying mutations in putative Ca2+ and caffeine-binding sites were functionally analysed. The results were interpreted with respect to recent near-atomic resolution RyR1 structures in various ligand states. We demonstrate that a tryptophan residue in the caffeine-binding site controls the structure of the Ca2+-binding site to regulate the Ca2+ sensitivity. Our results reveal the initial step of RyR channel activation by Ca2+ and explain the molecular mechanism of Ca2+ sensitization by caffeine and disease-causing mutations.
Ryanodine receptors (RyRs) are Ca2+ release channels in the sarcoplasmic reticulum of skeletal and cardiac muscles that play a pivotal role in excitation-contraction coupling1,2. RyRs are huge (~2 MDa) homotetrameric protein complexes with a large cytoplasmic structure and a cation channel domain of six transmembrane segments at the carboxyl (C)-terminus3,4. Type 1 RyR (RyR1) is a skeletal muscle isoform and mutations in RYR1 cause several muscle diseases, including malignant hyperthermia and central core disease5,6. Type 2 RyR (RyR2) is expressed mainly in the heart, and mutations in RYR2 are associated with various arrhythmogenic heart diseases, including catecholaminergic polymorphic ventricular tachycardia (CPVT)7,8. To date, a total of nearly 800 disease-related mutations have been identified in RYR1 and RYR2 genes.
The RyR channel mediates Ca2+-induced Ca2+ release (CICR), in which the channel is directly activated by Ca2+2,9. The binding of Ca2+ to the Ca2+-binding site is an initial step for channel activation9; therefore, regulation of the Ca2+-binding is important for channel activity and is implicated in disease states. Indeed, CICR activity is enhanced by many RYR1 mutations found in malignant hyperthermia and central core disease10,11,12 and by RYR2 mutations identified in CPVT13,14,15. The molecular details of the Ca2+ binding site and its regulation, however, remain largely unknown.
Recent cryo-electron microscopy structures of RyR1 and RyR2 have revealed a complex architecture, involving a superhelical scaffold in the cytoplasmic domain and a channel domain of the voltage-gated ion channel superfamily16,17,18,19,20. Furthermore, des Georges et al.20 reported putative binding sites for three major activating ligands, Ca2+, ATP, and caffeine, on a near-atomic resolution structure of RyR1. They proposed that the Ca2+-binding site is located in the core domain just above the transmembrane domain (Fig. 1a, b) and consists of several negatively charged residues in the core solenoid (CSol) domain and carboxyl-terminal domain (CTD) (Fig. 1c). Caffeine, a xanthine derivative, is a potent and common activator of all known RyR isoforms and greatly enhances Ca2+ sensitivity of the channel21,22. The putative caffeine-binding site is located just below the Ca2+-binding site and consists of several hydrophobic residues from different domains (Fig. 1d). The close proximity of Ca2+- and caffeine-binding sites suggests direct links between the two sites in regulating Ca2+ sensitivity. Indeed, a missense mutation (W4645R) of a tryptophan in the putative caffeine-binding site of human RyR2 has been reported to cause CPVT23, indicating the physiological significance of the caffeine-binding site.
To elucidate the molecular basis of Ca2+ binding for channel activation and to assess the role of this mechanism in disease states, we conducted functional analysis of RyR1 and RyR2 channels carrying mutations in these sites using a heterologous expression system in HEK293 cells. Based on high similarity in ligand-binding sites between RyR1 and RyR2, the results were interpreted with respect to recently reported near-atomic resolution structures of RyR1. We identified these as the actual binding sites and demonstrate that a tryptophan residue in the caffeine-binding site controls the structure of the Ca2+-binding site to regulate the Ca2+ sensitivity. Our results reveal the initial step of RyR channel activation by Ca2+ and explain the molecular mechanism of Ca2+ sensitization by caffeine and disease-causing mutations.
Tryptophan affects caffeine response and Ca2+ sensitivity
As a first step to address the molecular mechanism of Ca2+ binding to RyRs and its regulation via the caffeine-binding site, we analysed a CPVT mutation in the putative caffeine-binding site of human RyR2 (W4645R)23. The corresponding mutation (W4644R, see Supplementary Table 1) was introduced in mouse RyR2, and the mutant channel was heterologously expressed in HEK293 cells, which do not express an endogenous RyR. An alanine-substituted mutant (W4644A) was also generated for comparison. Expression of the mutant RyR2 was confirmed by Western blotting (Supplementary Figure 1).
The phenotype of the mutant RyR2 channel was initially investigated by monitoring intracellular Ca2+ homeostasis of HEK293 cells using G-GECO1.1 and R-CEPIA1er to simultaneously detect Ca2+ in the cytoplasm ([Ca2+]i) and ER lumen ([Ca2+]ER), respectively15 (Fig. 2a–c). [Ca2+] is expressed as (F − Fmin)/(Fmax− Fmin), in which Fmin and Fmax were determined in the presence of ionomycin with 1,2-bis(o-aminophenoxy)ethane-N,N,N’,N’-tetraacetic acid (BAPTA) plus cyclopiazonic acid and CaCl2, respectively (Supplementary Figure 2). In cells expressing WT RyR2, spontaneous Ca2+ oscillations occurred with concomitant decrease in [Ca2+]ER, indicating Ca2+ release from ER via the RyR2 channels (Fig. 2a). Cells expressing W4644R and W4644A RyR2 showed more frequent Ca2+ oscillations with reduced [Ca2+]ER compared to the WT RyR2 cells (Fig. 2b–d). Tetracaine, a known RyR inhibitor, effectively suppressed Ca2+ oscillations and greatly increased [Ca2+]ER of the mutant RyR2 cells (Supplementary Figure 3). These features have been shown to be typical gain-of-function phenotype of CPVT mutants15,24. In the WT RyR2 cells, caffeine triggered massive Ca2+ release from the ER (Fig. 2a). However, it did not trigger Ca2+ release or affect Ca2+ oscillations of the mutant RyR2 cells, suggesting that these mutants are unresponsive to caffeine (Fig. 2b–d).
Next, we determined Ca2+-dependent [3H]ryanodine binding to microsomes isolated from HEK293 cells. Since ryanodine specifically binds to the open RyR channel, amount of bound [3H]ryanodine quantitatively monitors the channel activity21,22. WT RyR2 exhibited biphasic Ca2+ dependence (Fig. 2e). W4644R and W4644A showed biphasic Ca2+ dependence with an enhanced Ca2+ sensitivity for activation (Fig. 2f, g). pCa value for 50% activation (pCa50) was greater in the mutants than in WT RyR2 (Fig. 2h). Again, W4644R and W4644A did not respond to caffeine, which greatly sensitized WT RyR2 to activation by Ca2+. Taken together, these results suggest that the tryptophan residue is essential for the action of caffeine. In addition, and more interestingly, the tryptophan is also involved in the physiological regulation of Ca2+ sensitivity.
To address whether the tryptophan residue is also important for the other RyR isoforms, we generated HEK293 cells that express RyR1 carrying alanine substitution of W4716 in the putative caffeine-binding site and performed functional analysis by Ca2+ imaging. Caffeine caused Ca2+ transients of WT RyR1 cells in a dose-dependent manner with an EC50 of ~1 mM11,12 (Supplementary Figure 4). W4716A RyR1 cells did not exhibit caffeine-induced Ca2+ transients, but they still responded to 4-CmC, another activator of the RyR1 channel25. These findings indicate an important role of the tryptophan residue in caffeine action in RyR1.
Tryptophan-mediated regulation of Ca2+ sensitivity
The putative binding sites for Ca2+ and caffeine are located close to each other (see Fig. 1); therefore, it is reasonable to expect that the caffeine-binding site directly regulates the Ca2+-binding site. To address the conformational changes caused by caffeine, it is necessary to compare the structure of RyR2 with or without caffeine. The structure of RyR2 with caffeine has not yet been solved and so we used RyR1 structures instead. The structures included RyR1 in the presence of caffeine plus ATP (Caf + ATP, PDB accession number 5TAP) (Fig. 3a), in the absence of Ca2+ (EGTA, 5TB0) (Fig. 3b), and in the presence of Ca2+ (5T15) (Fig. 3c). Comparison of the Caf + ATP and EGTA structures revealed that orientation of the tryptophan indole group (W4716 in RyR1 and W4644 in RyR2) is dynamically changed by the binding of caffeine (Fig. 3d). In addition, the size of the Ca2+-binding pocket is smaller in the Caf + ATP structure (the area demarked by the dotted circle in Fig. 3b is ~38 Å2, while the equivalent area shown in Fig. 3a is ~24 Å2), which is brought about by a ~2 Å upward shift of the CTD (Fig. 3d, black arrow) and a ~2 Å rightward shift of the CSol (Fig. 3d, white arrow). Interestingly, the overall structure around the Ca2+-binding site in Caf + ATP closely resembles that in the Ca2+ bound structure (Fig. 3e). Moreover, the size of the Ca2+-binding pocket in the two states is similar (the dotted circle shown in Fig. 3c is ~22 Å2). Thus, the Ca2+-binding site in the presence of caffeine appears more favorable for the binding of Ca2+ compared with the site in the absence of caffeine. This conformational change reasonably explains enhancement of Ca2+ sensitivity by caffeine.
By looking at the binding site in more detail, we found that isoleucine (I4996 in RyR1 and I4925 in RyR2) in the CTD is located close to the tryptophan in the EGTA state (Fig. 3b). Based on the finding, we hypothesized that an interaction between the tryptophan and the isoleucine may stabilize the CTD toward S2S3 (Fig. 3g). This may make the Ca2+-binding pocket larger and less favorable for the binding of Ca2+. The binding of caffeine will alter the orientation of the tryptophan indole group, which breaks the interaction causing movement of the CTD upward to make the Ca2+-binding pocket smaller and more favorable for Ca2+ binding. This reasonably explains why the CPVT mutant (W4644R) enhances the Ca2+ sensitivity; the mutated residues may weaken the interaction to move the CTD upward.
The amino acid residues around the putative Ca2+- and caffeine-binding sites are well conserved in three RyR isoforms (Supplementary Figure 5). We therefore compared structures of the putative Ca2+- and caffeine-binding sites of pig RyR2 in the presence of Ca2+ and in its absence (with EGTA) using available PDB data19 (Supplementary Figure 6). The overall structures and conformational changes by Ca2+ resembled those of RyR1: (1) the Ca2+-binding pocket was considerably smaller in the presence of Ca2+ compared with EGTA, (the area demarked by the dotted circle in Supplementary Figure 6 is ~34 Å2 in EGTA, while the equivalent area shown in the presence of Ca2+ is ~18 Å2), (2) the CTD moved upward in the presence of Ca2+ (~3 Å), (3) the CSol moved to the right in the presence of Ca2+ (~3 Å), and (4) hydrophobic residues responsible for caffeine action (tryptophan, isoleucine, and phenylalanine) are all conserved in RyR2.
Negatively charged and polar residues in the Ca2+-binding site
To verify the above hypothesis, we at first analysed the putative Ca2+-binding site, in which Ca2+ is proposed to be coordinated directly by E3893, E3967, and the carbonyl oxygen of T5001, and also indirectly by Q397020 in RyR1 (Fig. 1). Mutations at the coordinated residues are expected to reduce affinity for Ca2+; therefore, Ca2+-dependent activation should shift toward higher Ca2+ concentrations. Thus, RyR2s carrying mutations in the corresponding residues were tested using a Ca2+-dependent [3H]ryanodine binding assay. For an accurate measurement of Ca2+ dependent activation, assays were carried out in the presence of high salt (1 M NaCl) and no Mg2+, which removes inactivation by low-affinity Ca2+/Mg2+-binding sites21,22. Under these conditions, WT RyR2 exhibited monophasic Ca2+ dependence with pCa50 of ~5 (Fig. 4a). Alanine substitution caused total loss of binding in E3847 and E3921, and greatly reduced the Ca2+ sensitivity in Q3924 (Fig. 4a–d). These functional results are consistent with the structural data, strongly supporting the proposed structure of the Ca2+-binding site. Interestingly, aspartate substitution caused different phenotypes in the two glutamates; E3847D showed minimal binding at higher Ca2+ concentrations (Fig. 4a), while E3921D exhibited similar Ca2+ sensitivity as the WT (Fig. 4b). In addition, glutamate substitution of the glutamine (Q3924E), the corresponding mutation in human RyR2 (Q3925E) being associated with arrhythmogenic diseases26, also reduced Ca2+ sensitivity (Fig. 4c). This suggests that the amide group of Q3924 has an important role in regulation of the Ca2+ sensitivity. Based on the structure, we propose that the amide group of Q3924 may form a hydrogen bond with the carbonyl oxygen of H4932 in the CTD which stabilizes the CSol-CTD interface (Fig. 4e).
Tryptophan and isoleucine negatively regulates Ca2+ sensitivity
We next verified our hypothesis in the putative caffeine-binding site. We generated two mutants, W4644I and W4644L. Since side chains of isoleucine and leucine are longer and more hydrophobic than that of alanine, it is expected that interaction with the isoleucine is partially preserved in these mutants (Fig. 5a). Consistent with the hypothesis, Ca2+ sensitivity of W4644I and W4644L was considerably lower than that of W4644A (Fig. 5b, c, f), although it was still higher than that of WT. Moreover, W4644I and W4644L did not respond to caffeine (Fig. 5b, c, f), indicating an essential role of the tryptophan residue in caffeine action.
If interaction between tryptophan and isoleucine is essential in the regulation of Ca2+ sensitivity, the isoleucine side chain should also have an important role in maintaining the interaction. We therefore mutated the isoleucine to alanine (I4925A). I4925A exhibited greatly enhanced Ca2+ sensitivity comparable to that of W4644A (Fig. 5d, f). Interestingly, Ca2+ sensitivity was not increased further in the double mutant (W4644A_I4925A) (Fig. 5e, f). These results indicate that the enhanced Ca2+ sensitivity in W4644A and I4925A mutants occurs through a common mechanism, and that the maximum effect was caused by just a single alanine substitution. Taken together, these findings strongly support our hypothesis that the interaction between tryptophan and isoleucine is essential in the regulation of Ca2+ sensitivity.
Ca2+-sensitizing effect via phenylalanine-tryptophan interaction
The above results appear to reasonably explain the Ca2+-sensitizing effect of caffeine by interaction between tryptophan and isoleucine. However, we found that caffeine further sensitized I4925A to Ca2+ (Fig. 5d, f). An additional mechanism of Ca2+-sensitizing effect of caffeine is necessary to explain this phenomenon, since the interaction is thought to be completely lost in I4925A. In the structures, we noticed that side chain of tryptophan (W4716 in RyR1 and W4644 in RyR2) gets to phenylalanine (F3753 in RyR1 and F3713 in RyR2) within ~2 Å in the presence of Caf + ATP (Fig. 3a). Thus, the rotated indole group of tryptophan is likely to interact with phenylalanine, which may cause a ~2 Å rightward shift of CSol to make the Ca2+-binding pocket more suitable for Ca2+.
To verify this possibility, we substituted the phenylalanine in RyR2 with alanine (F3713A). Loss of phenylalanine side chain is expected to weaken the interaction, which causes a reduced Ca2+ sensitizing effect of caffeine (Fig. 6a). In the absence of caffeine, F3713A exhibited a reduced [3H]ryanodine binding with slightly higher Ca2+ sensitivity (pCa50 = 4.93 ± 0.03) than WT (pCa50 = 4.79 ± 0.03) (Fig. 6b, e). Caffeine sensitized the mutant to Ca2+, but the effect was rather weak compared with WT (Fig. 6b, c, e). We next tested the effect of the F3713A mutation on I4825A. If the phenylalanine-tryptophan interaction is responsible for an additional Ca2+ sensitization mechanism, the double mutant (F3713A_I4925A) should be unresponsive to caffeine (Fig. 6a). The Ca2+ sensitivity of F3713A_I4925A was as high as that of I4925A, but was not further sensitized by caffeine at all (Fig. 6d, e). These results support the above hypothesis that the phenylalanine-tryptophan interaction mediates an additional mechanism of caffeine action.
To address whether isoleucine and phenylalanine residues are also important for RyR1, functional analysis was done with HEK293 cells that express RyR1 carrying I4966A or F3753A mutation (Supplementary Figure 4). I4966A showed higher caffeine sensitivity with a reduced amplitude in caffeine-induced Ca2+ release, indicating a typical gain-of-function phenotype11,12. F3573A was much less responsive to caffeine in releasing Ca2+ compared with WT. The fact that 4-CmC caused large Ca2+ release in F3753A suggests similar level of ER Ca2+ as in WT. A caffeine-sensitive gain-of-function of I4996A and a reduced caffeine sensitivity of F3753A are consistent with the phenotype of I4925A and F3713A in RyR2, respectively.
Caffeine-binding site is a target for disease-associated mutations
Many disease-associated mutations have been found around ligand-binding sites in human RyR227. By functional screening of these mutations, we identified two CPVT mutations in human RyR2, C4193W28 and A4607P29, which greatly enhance the Ca2+ sensitivity. C4193W mutation was de novo and a patient suffered from syncope exhibited bidirectional ventricular tachycardia after the exercise stress test (Supplementary Figure 7). In the RyR1 structure, a corresponding cysteine (C4238) is located in the helix of the TaF domain, which is located just beneath the CTD, whereas a corresponding alanine (A4678) exists in the helix of S2S3, which is in close proximity to W4716 (Fig. 3). The two corresponding mutants (C4192W and A4606P) in mouse RyR2 demonstrated eightfold higher Ca2+ sensitivity than WT in [3H]ryanodine binding (Fig. 7a–c). Based on our calculation with the three parameters for CICR, the channel activity of these mutants was estimated to be more than 60-fold greater than that of WT at resting (100 nM) Ca2+ (Supplementary Figure 8), suggesting an arrhythmogenic potential. Interestingly, they exhibited different responses to caffeine: C4192W was further sensitized to Ca2+ by caffeine, but no activation was observed in A4606P (Fig. 7a–c). In HEK293 cells, C4192W demonstrated frequent Ca2+ oscillations with a reduced [Ca2+]ER (Fig. 7d). A4606P cells exhibited a reduced [Ca2+]ER but no Ca2+ oscillations (Fig. 7e, Supplementary Figure 2). Tetracaine greatly increased [Ca2+]ER of these mutant RyR2 cells (Supplementary Figure 3), indicating a gain-of-function phenotype. Again, caffeine caused massive Ca2+ release from the ER in C4192W but not in A4606P (Fig. 7d–f).
The phenotypes of these mutations could be explained by molecular mechanisms (Fig. 3). In cysteine-to-tryptophan mutation, steric hindrance may occur between the large indole group of tryptophan and α-helix of the CTD, in which the isoleucine is located. This may disrupt the interaction between tryptophan and isoleucine but may not affect positioning or orientation of tryptophan side chain; therefore, the mutant can still respond to caffeine via the phenylalanine-tryptophan interaction, as shown with isoleucine-to-alanine mutant (see Fig. 5c). In alanine-to-proline mutation, in contrast, incorporation of proline would kink the helix to alter the structure of the S2S3 helix, affecting the positioning or orientation of tryptophan side chain to disable caffeine binding, as observed with tryptophan-substituted mutants (see Fig. 2).
Ca2+ binding is the initial step in the activation of RyR channels and Ca2+ sensitivity is crucial for channel regulation. However, the molecular mechanism and regulation of the Ca2+ binding is poorly understood. In this study, we addressed this question by a combination of phenotype analysis of various RyR mutants, and interpretation by recently reported structures of the putative Ca2+- and caffeine-binding sites of RyR1 at near-atomic resolution. We verified the proposed binding sites to be the actual binding sites. Furthermore, we demonstrated that (1) the caffeine-binding site negatively regulates the Ca2+ sensitivity through an interaction between tryptophan in S2S3 and isoleucine in CTD, (2) caffeine sensitizes RyR to Ca2+ in two ways: by breaking the interaction between the tryptophan and the isoleucine and by forming another interaction between the tryptophan and a phenylalanine in Csol, and (3) CPVT mutations weaken the tryptophan-isoleucine interaction to enhance the Ca2+ sensitivity. Thus, the tryptophan residue serves as a switch to regulate the Ca2+ sensitivity. Our findings revealed the molecular basis for Ca2+ binding to RyR and provide an explanation for disease states.
We performed phenotype analysis of the mutant RyRs using intracellular Ca2+ ([Ca2+]i and [Ca2+]ER) measurements and [3H]ryanodine binding. These assays measure the activity of the RyR channels21,22. Thus, our results by functional analysis provide an indirect evidence for binding of Ca2+ or caffeine to their binding sites. However, highly quantitative nature of [3H]ryanodine binding enabled us to address the Ca2+ sensitivity and the effect of caffeine in the mutant RyRs. We interpreted the functional results of mouse RyR2 with rabbit RyR1 structure, since there is no structural information about the Ca2+- and caffeine-binding sites in the reported RyR2 structure19. One might concern about misinterpretation by different isoforms. However, we are confident of our strategy for the following reasons. First, the effect of caffeine is common between RyR1 and RyR221,22. Second, the residues responsible for caffeine binding are highly conserved within the three mammalian RyR isoforms (Supplementary Figure 5). Third, structures of Ca2+- and caffeine-binding sites and conformational change by Ca2+ are common between RyR1 and RyR2 (Supplementary Figure 6). Finally, the proposed mechanism can reasonably explain the phenotypes of RyR1s carrying mutations at hydrophobic residues in the caffeine-binding sites (Supplementary Figure 4). These findings strongly indicate that the strategy used in this study is valid and the conclusions can be commonly applied to both RyR1 and RyR2.
In the putative Ca2+-binding site, Ca2+ is surrounded by negatively charged residues, including two glutamate residues and one glutamine residue20 (Fig. 1). It has been proposed that the glutamate residues are involved in direct coordination of Ca2+, whereas the glutamine residue may contribute to indirect Ca2+ coordination20. We showed that alanine substitution of glutamates completely abolished Ca2+-dependent [3H]ryanodine binding, whereas that of glutamine greatly reduced but not abolished the Ca2+ sensitivity (Fig. 4). These findings strongly support the proposed model of the Ca2+-binding site. The functional analysis also provided important information about Ca2+-binding sites that has not been predicted. First, aspartate substitution of the two glutamates caused different phenotypes: E3847D caused a severe reduction in Ca2+ sensitivity, whereas E3921D exhibited no or only minor change. This implies that the approximate location of these residues against Ca2+ is different: E3921 might be more closely located to Ca2+ than E3847. Second, Q3924E caused a great reduction of Ca2+ sensitivity, indicating an importance of the amide group of the glutamine. Based on the structure, we propose that the amide group of the glutamine may form a hydrogen bond with the carbonyl oxygen of histidine in the CTD to stabilize the CSol-CTD interface (Fig. 4).
The putative caffeine-binding site of RyR1 consists of hydrophobic residues, i.e., tryptophan, isoleucine and phenylalanine (Fig. 1), among which tryptophan has been predicted to be most important for caffeine binding20. We demonstrated that mutations at the tryptophan in RyR1 (Supplementary Figure 4) and RyR2 (Fig. 2) caused complete loss of caffeine action. This strongly supports the proposed model of caffeine-binding site. In contrast, caffeine still enhanced the Ca2+ sensitivity of the mutant carrying an alanine substitution of isoleucine (Fig. 5) or phenylalanine (Fig. 6). Thus, these residues are not essential for caffeine binding; rather they contribute to Ca2+ sensitization by caffeine via interaction with the tryptophan.
Our current working model of regulation of the Ca2+-binding site by caffeine-binding site is as follows. In the absence of caffeine, interaction between tryptophan in S2S3 and isoleucine in CTD keeps the lower half of the Ca2+-binding site in CTD apart from the upper half in the CSol. This makes the Ca2+-binding pocket larger and less favorable for Ca2+ binding. Caffeine binds to the caffeine-binding site so as to align in parallel with an indole group of the tryptophan by rotating its side chain. This breaks the tryptophan-isoleucine interaction, leading to upward shift of CTD by a ~2 Å toward the upper half of the Ca2+-binding site to make Ca2+-binding pocket smaller that is more favorable for Ca2+ binding (Fig. 3). In addition, side chain of the tryptophan then interacts with phenylalanine in CSol, which causes rightward shift of the upper half of the Ca2+-binding site by a ~2 Å to make the Ca2+-binding pocket more suitable for Ca2+ binding (Fig. 5). The two mechanisms are independent of each other and cooperatively sensitize the channel to activating Ca2+.
The presence of two Ca2+ sensitizing mechanisms raises the question of their relative contributions. This could be answered by phenotypes of mutants lacking either interaction. The Ca2+ sensitization effect of caffeine on phenylalanine-to-alanine mutant was about half that on WT (Fig. 6). On the other hand, isoleucine-to-alanine mutant exhibited 10-fold greater Ca2+ sensitivity than WT in the absence of caffeine, and caffeine further sensitized the mutant to Ca2+ by 10-fold (Fig. 5). Taken together, we estimate that the two mechanisms have roughly the same contribute to the Ca2+ sensitization by caffeine. Another question is which kind of interactions occurs in the caffeine-binding site. Since tryptophan, isoleucine, and phenylalanine are all hydrophobic residues, hydrophobic interactions by van der Waals force are mostly plausible. Alternatively, steric effect of tryptophan residue is also possible since tryptophan has a bulky side chain. More detailed structures will provide evidence for the underlying mechanism of interactions.
We used the structure of RyR1 with caffeine plus ATP (5TAP), due to no other available structures with caffeine. This might raise a concern that some structure changes in the Ca2+-binding and caffeine-binding sites are caused by ATP. However, the putative binding site of ATP is ~25 Å apart from the caffeine-binding site20. In addition, it has been shown that ATP does not change the Ca2+ sensitivity nor influence the Ca2+-sensitizing action of caffeine21,22. Thus, it seems unlikely that ATP directly affects the caffeine-binding site, although we cannot completely exclude the possibility.
We demonstrate that conformation of the Ca2+-binding site with Caf + ATP (5TAP) is overlapped with that with Ca2+ (5T15) (Fig. 3). One possible assumption is that caffeine can mimic the conformational change induced by Ca2+. However, functional analysis revealed that Ca2+ is essential for activation of the RyR channels even in the presence of caffeine (see Fig. 2). des Georges et al.20 demonstrated that conformation with Ca2+ or with Caf + ATP is in the primed state, in which the cytoplasmic assembly and activation module are moved but the gate remains closed, and that all the three ligands can induce further conformational changes to open the gate. Indeed, dynamic conformational changes occur in the Ca2+-binding and caffeine-binding sites in the structure with Ca2+/Caf/ATP (5T9V) (Supplementary Figure 9).
Since the caffeine-binding site negatively regulates the channel by reducing Ca2+ sensitivity, it is reasonable to expect that mutations disrupting the caffeine-binding site sensitize the channel to Ca2+ to cause disease. Indeed, we demonstrate that a CPVT mutation in tryptophan in the caffeine-binding site (W4645R in human RyR223) greatly sensitizes the RyR2 channel to Ca2+ (Fig. 2). We also identified two additional CPVT mutations near the caffeine-binding site in human RyR2, C4193W28 and A4607P, that exhibit enhanced Ca2+ sensitivity (Fig. 7). Thus, the caffeine-binding site and the surrounding regions are candidates for disease-associated mutations in RyR2. A similar situation may also occur with RyR1, although we could not detect corresponding mutations in RyR1. RyRs exhibit global conformational changes upon channel activation19,20,30,31; therefore, it is possible that certain mutations apart from those in the Ca2+- and caffeine-binding sites also affect these sites by a long-range allosterism. Comprehensive functional analysis of the mutant channels will provide more information.
What we propose in this study is a very simple and clear-cut mechanism of Ca2+ sensitization by the caffeine-binding site. Thus, it is highly possible that the site functions physiologically in vivo. Caffeine is a xanthine derivative (methylxanthine) produced in plants32. Although methylxanthines are not present in animals, including humans, xanthine is a metabolite of purine nucleotides in humans. It has been reported that 9-methyl-7-bromoeudistomin D (MBED), an artificial β-carboline analogue, has a potent Ca2+ releasing activity by binding to the caffeine-binding site33. Some β-carbolines may be formed naturally in humans34. Thus, it is quite possible that some derivatives of xanthine or β-carbolines act as the endogenous regulators of RyRs through the caffeine-binding site to regulate physiological Ca2+ sensitivity in vivo.
Generation of stable inducible HEK293 cell lines
HEK293 cells, stably and inducibly expressing WT and mutant forms of RyR112 and RyR215 were generated using the Flp-In T-REx system (Life Technologies, CA, USA). Each mutation was introduced into rabbit RyR1 (GenBank accession number X15209.1) or mouse RyR2 (NM_023868.2) cDNA by inverse polymerase chain reaction using primers listed in Supplementary Table 2. The mutated cDNA fragment was subcloned into the expression vector (pcDNA5/FRT/TO). Flp-In T-REx HEK293 cells were maintained in Dulbecco’s modified Eagle’s media supplemented with 10% fetal calf serum and 2 mM L-glutamine. The stable inducible cell lines were generated by co-transfection of the expression vector with the pOG44 vector encoding Flp recombinase according to the manufacturer’s instructions. Transfected cells were re-plated one day after transfection and the growth medium was replaced with selective medium containing 100 µg ml−1 hygromycin. The selective medium was changed every three days until the hygromycin-resistant foci were identified. Several hygromycin-resistant foci were tested for the inducible expression of RyRs and clones with suitable expression were selected and used for experiments.
Single-cell Ca2+ imaging
Single-cell Ca2+ imaging was carried out in HEK293 cells expressing WT or mutant RyR1 and RyR215,35. In Ca2+ measurements with RyR2, the Ca2+ signals from cytoplasm ([Ca2+]i) and ER lumen ([Ca2+]ER) were monitored using G-GECO1.1 (a gift from Robert Campbell from University of Alberta, Addgene plasmid # 32445)36 and R-CEPIA1er (a gift from Masamitsu Iino, The University of Tokyo)37, respectively. Cells were transfected with cDNAs for these Ca2+ indicators 28–32 h before measurement. Expression of RyR2 was induced by doxycycline (2 µg/ml) 4–6 h before measurement depending on the mutant. Experiments were carried out with HEPES-buffered Krebs solution (140 mM NaCl, 5 mM KCl, 2 mM CaCl2, 1 mM MgCl2, 11 mM glucose and 5 mM HEPES at pH 7.4). In experiments with RyR1, cells were loaded with fluo-4 AM 24 h after induction and fluorescence signals in response to caffeine (0.03–10 mM) were determined. At the end of each experiment, Fmin and Fmax were obtained with 0Ca Krebs solution containing 20 µM ionomycin, 5 mM BAPTA, and 20 µM cyclopiazonic acid and 20Ca Krebs solution containing 20 µM ionomycin and 20 mM CaCl2, respectively15. Averaged Fmin was 7.655% of Fmax for R-CEPIA1er and 0% for G-GECO1.1 and fluo-4. The fluorescence signal (F − Fmin) was normalized to the maximal fluorescence intensity (Fmax− Fmin). Measurements were carried out at 26°C.
Preparation of microsomes
HEK293 cells expressing RyR2 mutants (5 × 150 mm dishes) were collected and rinsed twice with phosphate-buffered saline. The cell pellets were resuspended with 5 ml of 0.3 M sucrose, 20 mM 3-morpholinopropanesulfonic acid (MOPS), pH 7.4 with a protease inhibitor cocktail and processed for nitrogen cavitation for 15 min at 1000 psi. The homogenate was centrifuged at 1000 × g for 5 min and the supernatant was ultracentrifuged for 30 min at 100,000 × g. The microsomal pellet was resuspended with 5 ml of the above buffer and ultracentrifuged again. The pellet was resuspended with 1 ml of the above buffer, quickly frozen with liquid nitrogen, and stored at −80 °C until used.
[3H]Ryanodine binding and parameter analysis
Microsomes isolated from HEK293 cells expressing WT and mutant RyR2 were incubated for 1 h at 25°C with 5 nM [3H]ryanodine in a medium containing 0.17 M NaCl, 20 mM 3-(N-morpholino)-2-hydroxypropanesulfonic acid (MOPSO) at pH 7.0, 2 mM dithiothreitol, 1 mM AMP, 1 mM MgCl2 and various concentrations of free Ca2+ buffered with 10 mM ethylene glycol-bis(2-aminoethylether)-N,N,N’,N’-tetraacetic acid (EGTA)15,35. Free Ca2+ concentrations were calculated using WEBMAXC STANDARD (http://web.stanford.edu/~cpatton/webmaxcS.htm)38. The [3H]ryanodine binding data (B) were normalized to the maximum number of functional channels (Bmax), which was separately determined by Scatchard plot analysis using varied concentrations (3–20 nM) of [3H]ryanodine in a high-salt medium. The resultant B/Bmax represents the averaged activity of each mutant. For mutants regarding the Ca2+-binding sites, medium containing 1 M NaCl and no Mg2+ was used to remove inactivation through the low-affinity Ca2+/Mg2+ site.
To determine the parameters of Ca2+-dependent activity, the data were fitted to the following equation:
where A is the binding at the specified Ca2+, Amax is the gain that determines the maximal attainable binding, and fA and fI are fractions of the activating Ca2+ site (A-site) and inactivating Ca2+ site (I-site) bound to Ca2+, respectively39. fA and fI at the specified Ca2+ concentration ([Ca2+]) are expressed as:
where KA and KI are dissociation constants, and nA and nI are Hill coefficients for Ca2+ of A- and I-sites, respectively. The Hill coefficients were set at 2.0 and 1.0 for nA and nI, respectively, for WT and all the mutant channels, which maximize the sum of R2 values for curve fitting. Curve fitting was performed using the Prism 6 software (GraphPad Software, La Jolla, CA, USA). The curves for fA, 1 – fI, and A are shown in Supplementary Figure 6. For estimation of CICR activity at resting [Ca2+]i, A at pCa = 7 was calculated by Eqs. (1–3) using the obtained parameters (KA, KI, and Amax).
Microsomal proteins (10 μg) were separated by sodium dodecyl sulfate polyacrylamide gel electrophoresis with a 3–12% gel and transferred onto a polyvinylidene fluoride membrane. Western blotting was performed using antibodies for pan RyR40 (1: 5000 dilution) and calnexin (C4731, Sigma-Aldrich, MO, USA) (1: 5000 dilution).
The patient carrying C4193W mutation in RyR228 was diagnosed with CPVT and introduced to Shiga University of Medical Science for genetic analysis. The patient and her family provided written informed consent in accordance with the guidelines approved by our institutional review boards (23-128-3). Genomic DNA was extracted from peripheral blood lymphocytes by use of the DNA Isolation Kit (Roche Diagnostics GmbH, Mannheim, Germany). Genetic screening for 50 genes related to inherited arrhythmias including RYR2, CASQ2, KCNJ2 and TRDN were performed by using a bench-top next generation sequencer (NGS) (MiSeq, Illumina, San Diego, CA, USA). Detected variants were confirmed by Sanger methods.
Statistical analysis was performed using Prism 6 (GraphPad Software, Inc., La Jolla, CA, USA). Unpaired two-tailed Student’s t-test and one-way ANOVA followed by Dunnett’s test, were performed to compare two groups and three or more groups, respectively. Structural figures were prepared with PyMOL (The PyMOL Molecular Graphics System, Schrödinger).
The authors declare that the data supporting the findings of this study are available within the paper and its supplementary information files. The PDB accession numbers we used in this paper are 5TAP, 5TB0, 5T15, 5T9V, 5GO9, 5GOA.
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We are grateful to the Laboratory of Molecular and Biochemical Research, Research Support Center, Juntendo University Graduate School of Medicine, for their technical support. We thank Jeremy Allen, PhD, from Edanz Group (https://nec.edanzediting.com) for editing a draft of this manuscript. This work was supported in part by Japan Society for the Promotion of Sciences KAKENHI (Grant Number JP16K08507 to T.M., JP16H04748 to H.O. and JP15K08243 to N.K.), Platform Project for Supporting Drug Discovery and Life Science Research (Basis for Supporting Innovative Drug Discovery and Life Science Research (BINDS)) (JP17am0101080j0001) to T.M. and H.O. and Practical Research Project for Rare / Intractable Diseases (JP17ek0109202h0001) to N.K., S.O. and M.H. from Japan Agency for Medical Research and Development (AMED), Intramural Research Grant (29-4) for Neurological and Psychiatric Disorders of National Center of Neurology and Psychiatry to T.M., the Vehicle Racing Commemorative Foundation (http://www.vecof.or.jp/) to N.K., the Institute of Seizon & Life Sciences (http://seizon.umin.jp/) to T.M., a grant from the Institute for Environmental & Gender-specific Medicine, Juntendo University to N.K. and Program for the Strategic Research Foundation at Private Universities supported by Ministry of Education, Culture, and Sports, Science and Technology, Japan.
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Journal of Neurology (2018)