Parameter values used to quantitatively describe the activation of DHPR-coupled RyR1s, cRyR1s, (cP0), and DHPR-noncoupled RyR1s, ncRyR1s (ncP0) under different conditions
| Parameter | Description | Parameter value |
|---|---|---|
| 1pKMm | Apparent dissociation constant of Mm+ from individual A-sites of cRyR1s and ncRyR1s | 172.1 mMa |
| 1pKL | Ca2+ equilibrium dissociation constant from individual SR luminal sites of cRyR1s and ncRyR1s | 346.6 μMa |
| 1pKMg | Mg2+ equilibrium dissociation constant from individual A-sites of cRyR1s and ncRyR1s | 30.65 μMa |
| 1pKCaA | Ca2+ equilibrium dissociation constant from individual A-sites of cRyR1s and ncRyR1s | 70 nMa |
| 1pPmax | Level of individual A-site activation in cRyR1s and ncRyR1s when the A-site is occupied by Ca2+ | 0.963a |
| 1pPi | Level of individual A-site activation in cRyR1s and ncRyR1s when the A-site is free or is occupied by two Mm+; 1pPi is sensitive to SR luminal Ca2+ ([Ca2+]L) | = 0.56 + 0.35/(1 + 0.25 mM/[Ca2+]L)a |
| Kin | Apparent Ca2+/Mg2+ dissociation constant from I1 sites of ncRyR1s | 0.05 mMb |
| 4pKin | Apparent Ca2+/Mg2+ dissociation constant from I1 sites of cRyR1s when DHPRs are not activated | 0.05 mMb |
| 4pKin | Apparent Ca2+/Mg2 dissociation constant from I1 sites of cRyR1s when the DHPRs are activated | 1.5 mMc |
| Parameter | Description | Parameter value |
|---|---|---|
| Apparent dissociation constant of Mm+ from individual A-sites of | 172.1 mM | |
| Ca2+ equilibrium dissociation constant from individual SR luminal sites of | 346.6 μM | |
| Mg2+ equilibrium dissociation constant from individual A-sites of | 30.65 μM | |
| Ca2+ equilibrium dissociation constant from individual A-sites of | 70 nM | |
| Level of individual A-site activation in | 0.963 | |
| Level of individual A-site activation in c | = 0.56 + 0.35/(1 + 0.25 mM/[ | |
| Apparent Ca2+/Mg2+ dissociation constant from I1 sites of | 0.05 mM | |
| Apparent Ca2+/Mg2+ dissociation constant from I1 sites of | 0.05 mM | |
| Apparent Ca2+/Mg2 dissociation constant from I1 sites of | 1.5 mM |
Parameter value derived in Appendix 1 from experimental data of Laver et al. (2004).
Parameter value derived from experimental data of Donoso et al. (2000).
As described in the text, DHPR activation of cRyR1s induces a sudden 30-fold rise of 4pKin from its resting level in cRyR1s, which eases inhibition at the I1-sites of the respective cRyR1s.
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