Journal
BIOPHYSICAL JOURNAL
Volume 87, Issue 3, Pages 1784-1794Publisher
CELL PRESS
DOI: 10.1529/biophysj.103.039131
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Funding
- NHLBI NIH HHS [HL 07403, R01 HL067071, R01 HL061683, HL 67071, T32 HL007403, R01 HL065497, HL 61683] Funding Source: Medline
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We examined the influence of cross-bridge cycling kinetics on the length dependence of steady-state force and the rate of force redevelopment (k(tr)) during Ca2+-activation at sarcomere lengths (SL) of 2.0 and 2.3 mum in skinned rat cardiac trabeculae. Cross-bridge kinetics were altered by either replacing ATP with 2-deoxy-ATP ( dATP) or by reducing [ ATP]. At each SL dATP increased maximal force (F-max) and Ca2+-sensitivity of force (pCa(50)) and reduced the cooperativity (n(H)) of force-pCa relations, whereas reducing [ATP] to 0.5 mM (low ATP) increased pCa(50) and n(H) without changing F-max. The difference in pCa(50) between SL 2.0 and 2.3 mum (DeltapCa(50)) was comparable between ATP and dATP, but reduced with low ATP. Maximal k(tr) was elevated by dATP and reduced by low ATP. Ca2+-sensivity of k(tr) increased with both dATP and low ATP and was unaffected by altered SL under all conditions. Significantly, at equivalent levels of submaximal force k(tr) was faster at short SL or increased lattice spacing. These data demonstrate that the SL dependence of force depends on cross-bridge kinetics and that the increase of force upon SL extension occurs without increasing the rate of transitions between nonforce and force-generating cross-bridge states, suggesting SL or lattice spacing may modulate preforce cross-bridge transitions.
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