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. Author manuscript; available in PMC: 2019 May 8.
Published in final edited form as: Hear Res. 2018 Nov 16;376:11–21. doi: 10.1016/j.heares.2018.11.002

TABLE 1.

Model parameters

MET Channel whole cell Ca2+ current 14 pA base, 4.0 pA apex (Johnson et al., 2011)
Fixed buffer1 Concentration 1 mM (stereocilia) (Xu et al., 1997)
dissociation coefficient 10 µM
forward binding rate 107 M−1s−1
Oncomodulin CalbindinD28k Concentration2 (mM) 4 mM (apex) 6 mM (base) (Hackney et al., 2005)
dissociation coefficient 0.5 µM (Lee et al., 2000)
forward binding rate3 2×107 M−1s−1 (Nagerl et al., 2000)
diffusion coefficient 50 µm2/s (Schmidt et al., 2003)
PMCA max. velocity of transport4 2.0 µmol/m2s (Beurg et al., 2010)
dissociation coefficient 0.5 µM (Carafoli et al., 1994)
Mitochondria Uniporter MCU transport rate5 114 mM/s (Wingrove et al., 1984)
dissociation coefficient 40 µM (Xu et al., 1997)
Mitochondria NCX transport rate 1.8 mM/s (Patterson et al., 2007)
dissociation coefficient 5 µM (Hilgemann et al., 1991)
1

Fixed buffer values are assumed based on ranges in different neuronal Ca2+ models. Ca2+ binding ratio, (total buffer concentration)/KCa =100:1 (Tucker & Fettiplace 1995)

2

This is the density of the Ca-binding sites, not the density of the molecules

3

This parameter value was unavailable for oncomodulin so value for calbindinD28k used instead.

4

2.0 μmol/m2s = (2000 pumps/μm2)×(600 ions/pumps/2) /(6.0×1023ions/mol)

5

This value is derived from Wingrove et al..(1984) Flux, J = 4 nmol/mg/min at C = 0.5 μM.