Table 1.

Parameter values used to quantitatively describe the activation of DHPR-coupled RyR1s, cRyR1s, (cP0), and DHPR-noncoupled RyR1s, ncRyR1s (ncP0) under different conditions

ParameterDescriptionParameter 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 
a

Parameter value derived in Appendix 1 from experimental data of Laver et al. (2004).

b

Parameter value derived from experimental data of Donoso et al. (2000).

c

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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