Figure 3
Figure 3. Estimation and analysis of platelet Ca2+ regulation. Unknown concentrations and compartment sizes in the platelet Ca2+ module were estimated by randomly sampling the unknown quantities in panel A and selecting only those molecular “configurations” that produced a resting [Ca2+]i of 100 plus or minus 10 nM. (B) This reduced set of configurations was divided into 3 groups based on the estimated [Ca2+]dts (top), which corresponded to the [Ca2+]i release behavior after a 10-fold increase in [IP3] (bottom). (C) Probability distributions for estimates of SERCA, IP3R, IP3, and the relative DTS volume in low-, mild-, and high-response configurations (n = 100 000). The measured IP3 level from resting platelets31 is boxed. (D) Image obtained from glucose-6-phosphatase stain of the DTS from a human platelet16 was used to quantify the cytosolic (gray) and DTS (black) area from a 2D section of the platelet.

Estimation and analysis of platelet Ca2+ regulation. Unknown concentrations and compartment sizes in the platelet Ca2+ module were estimated by randomly sampling the unknown quantities in panel A and selecting only those molecular “configurations” that produced a resting [Ca2+]i of 100 plus or minus 10 nM. (B) This reduced set of configurations was divided into 3 groups based on the estimated [Ca2+]dts (top), which corresponded to the [Ca2+]i release behavior after a 10-fold increase in [IP3] (bottom). (C) Probability distributions for estimates of SERCA, IP3R, IP3, and the relative DTS volume in low-, mild-, and high-response configurations (n = 100 000). The measured IP3 level from resting platelets31  is boxed. (D) Image obtained from glucose-6-phosphatase stain of the DTS from a human platelet16  was used to quantify the cytosolic (gray) and DTS (black) area from a 2D section of the platelet.

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