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. 2021 Apr 1;4:163–176. doi: 10.1016/j.crphys.2021.03.005

Table 3.

Energy penalty for mitochondria with lamellar and tubular cristae.

A) Crista Shape KINASE
(rel)
J(AS)
(mol/μm2/ms)
SCRIS
(μm2)
ATP OUTPUT q ​= ​J(AS) × SCRIS
(mol/ms)
ENERGY PENALTY
Δq ​= ​[Jmax(AS) - J(AS)] × SCRIS
(mol/ms)
Δq/qmax
(%)
q/qo
LAM SLOW 74.5 4.8 358 118 25 2.0
FAST 85.5 410 65 14 2.3
TUB SLOW 84 4.1 344 61.5 15 1.9
FAST 90 369 37 9 2.1
NONE (o) SLOW 99 1.8 178 0 0 1
FAST 99 178 0 0 1
B) Crista Shape KINASE
(rel)
J(AS)
(mol/μm2/ms)
SCRIS
(μm2)
ATP OUTPUT q ​= ​J(AS) × SCRIS
(mol/ms)
ENERGY PENALTY
Δq ​= ​[Jmax(AS) - J(AS)] × SCRIS
(mol/ms)
Δq/qmax
(%)
q/qo
LAM SLOW 38 37.4 1421 2281 62 4.2
FAST 67 2506 1197 32 7.4
TUB SLOW 59 20.4 1204 836 41 3.6
FAST 74 1510 510 25 4.5
NONE (o) SLOW 99 3.4 337 0 0 1
FAST 99 337 0 0 1

Effects of crista morphology and kinase activity on ATP output (q) for lamellar (LAM) and tubular (TUB) spatial models of the mitochondrial inner membrane, relative to a model with no cristae (NONE). Results in Table A (upper) correspond to fluxes of ATP synthase, J(AS), and IM surface areas, SIM, for the largest 3D spatial models used for computer simulations with the reduced BioModel. Results in Table B (lower) correspond to J(AS) values extrapolated for rat cardiac muscle mitochondria (see text), using the linear regression equations in Fig. 6B. Kinase activities are labelled SLOW and FAST, corresponding to forward reaction constants (kf) of 0.003 and 0.009 msec−1, respectively. Other abbreviations: mol ​= ​molecules, ms ​= ​millisecond, qo ​= ​ATP output for the model with no cristae, qmax ​= ​hypothetical q for a model with cristae calculated using J(AS) for the model with no cristae, Jmax(AS).