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. Author manuscript; available in PMC: 2019 Jul 18.
Published in final edited form as: Circulation. 2019 May 14;139(20):2358–2371. doi: 10.1161/CIRCULATIONAHA.118.039329

Table 1. Concentration and properties of the major cellular buffers in ventricular myocytes.

Concentration Kd On rate

μmol/L cell cytoplasm μM M-1.s-1

Ca buffers

Troponin C (regulatory) 9, 10 70 0.6 3.27x107

SERCA11 47 0.6 1.00 x108

Calmodulin3 24 7 3.4 x107

Sarcolemma (low)12 42 13 1.0 x108

Sarcolemma (high) 12 15 0.3 1.0 x108

Ca/Mg buffers

Troponin C (Mg) 9, 13 140 0.0195 3.3 x103

Myosin9 140 4.62 9.6 x104

ATP14 5000 1200 1.9 x106

Histidyl dipeptides15, 16 20000 1000 6.1 x106

Chemical probes

BAPTA17 0.178 5.0 x108

EGTA18 (pH7.2) 0.180 2.3 x106

The cellular buffers are organized in two groups: top, Ca buffers; middle Ca/Mg buffers. The properties of two chemical agents (BAPTA & EGTA) are shown below. For the cellular buffers, the first two columns show the buffer concentration and its Kd. The third column gives the value of the on rate constant for Ca2+ binding to the buffer. This has been calculated under standard conditions (initial free [Ca2+] 100 nM, addition of 10 μM Ca2+ to 10 μM buffer). The value for calmodulin is an approximation to one binding site 11. For the Mg/Ca buffers the Kd and rate constant have been corrected for the apparent value in the presence of a cellular Mg2+ of 0.5 mM.

Indicates rate constant was estimated based on diffusion limit.