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. 2016 Aug 24;311(5):C749–C757. doi: 10.1152/ajpcell.00134.2016

Table 2.

Activation of wild-type and mutant RyRs by Ca2+

EC50, μM
Mutation Myopathy No Mg2+ 1 mM Mg2+
WT-RyR1 1.0 ± 0.1 (5) 2.0 ± 0.1 (4)
EF-hand T4082M MH 0.74 ± 0.08 (5) ND
S4113L CNM 1.2 ± 0.1 (5) ND
N4120Y MH 0.91 ± 0.11 (5) ND
S2–S3 loop F4732D MH 0.66 ± 0.13 (4) 1.4 ± 0.2 (7)
G4733E MH 0.73 ± 0.05 (4) 1.4 ± 0.2 (5)
R4736W MH 0.96 ± 0.09 (7) 1.4 ± 0.1 (5)
R4736Q MH 1.2 ± 0.1 (5) 1.4 ± 0.2 (6)
S4–S5 loop T4825I MH 0.22 ± 0.02*(6) 0.94 ± 0.05* (4)
H4832Y MH 0.41 ± 0.09*(5) 0.51 ± 0.03* (4)
WT-RyR2 4.2 ± 2.5 (5) 1.9 ± 0.04 (8)

Values are means ± SE of the number of experiments indicated in parentheses. EC50 values for Ca2+-dependent activation of wild-type and mutant RyRs were determined in the absence and presence of 1 mM Mg2+. RyR1 mutations are associated with either malignant hyperthermia (MH) or centronuclear myopathy (CNM).

*

P < 0.05 compared with WT-RyR1 by one-way ANOVA followed by Tukey's test among RyR1 groups (wild-type and mutant RyR1s). ND, not determined.