Abstract
ATP, 2-deoxy ATP (dATP), CTP, and UTP support isometric force and unloaded shortening velocity (Vu) to various extents (Regnier et al., Biophys. J. 74:3044-3058). Vu correlated with the rate of cross-bridge dissociation after the power stroke and the steady-state hydrolysis rate in solution, whereas force was modulated by NTP binding and cleavage. Here we studied the influence of posthydrolytic cross-bridge steps on force and fiber shortening by measuring isometric force and stiffness, the rate of tension decline (kPi) after Pi photogeneration from caged Pi, and the rate of tension redevelopment (ktr) after a sudden release and restretch of fibers. The slope of the force versus [Pi] relationship was the same for ATP, dATP, and CTP, but for UTP it was threefold less. ktr and kPi increased with increasing [Pi] with a similar slope for ATP, dATP, and CTP, but had an increasing magnitude of the relationship ATP < dATP < CTP. UTP reduced ktr but increased kPi. The results suggest that the rate constant for the force-generating isomerization increases with the order ATP < dATP < CTP < UTP. Simulations using a six-state model suggest that increasing the force-generating rate accounts for the faster kPi in dATP, CTP, and UTP. In contrast, ktr appears to be strongly affected by the rates of NTP binding and cleavage and the rate of the force-generating isomerization.
Full Text
The Full Text of this article is available as a PDF (178.1 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Araujo A., Walker J. W. Phosphate release and force generation in cardiac myocytes investigated with caged phosphate and caged calcium. Biophys J. 1996 May;70(5):2316–2326. doi: 10.1016/S0006-3495(96)79797-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Brenner B. Effect of Ca2+ on cross-bridge turnover kinetics in skinned single rabbit psoas fibers: implications for regulation of muscle contraction. Proc Natl Acad Sci U S A. 1988 May;85(9):3265–3269. doi: 10.1073/pnas.85.9.3265. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Brenner B., Eisenberg E. Rate of force generation in muscle: correlation with actomyosin ATPase activity in solution. Proc Natl Acad Sci U S A. 1986 May;83(10):3542–3546. doi: 10.1073/pnas.83.10.3542. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chase P. B., Martyn D. A., Hannon J. D. Isometric force redevelopment of skinned muscle fibers from rabbit activated with and without Ca2+. Biophys J. 1994 Nov;67(5):1994–2001. doi: 10.1016/S0006-3495(94)80682-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cooke R., Franks K., Luciani G. B., Pate E. The inhibition of rabbit skeletal muscle contraction by hydrogen ions and phosphate. J Physiol. 1988 Jan;395:77–97. doi: 10.1113/jphysiol.1988.sp016909. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cuda G., Pate E., Cooke R., Sellers J. R. In vitro actin filament sliding velocities produced by mixtures of different types of myosin. Biophys J. 1997 Apr;72(4):1767–1779. doi: 10.1016/S0006-3495(97)78823-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dantzig J. A., Goldman Y. E., Millar N. C., Lacktis J., Homsher E. Reversal of the cross-bridge force-generating transition by photogeneration of phosphate in rabbit psoas muscle fibres. J Physiol. 1992;451:247–278. doi: 10.1113/jphysiol.1992.sp019163. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ferenczi M. A., Spencer C. I. The elementary steps of the actomyosin ATPase in muscle fibres studied with caged-ATP. Adv Exp Med Biol. 1988;226:181–188. [PubMed] [Google Scholar]
- Goldman Y. E., Hibberd M. G., Trentham D. R. Relaxation of rabbit psoas muscle fibres from rigor by photochemical generation of adenosine-5'-triphosphate. J Physiol. 1984 Sep;354:577–604. doi: 10.1113/jphysiol.1984.sp015394. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kentish J. C. Combined inhibitory actions of acidosis and phosphate on maximum force production in rat skinned cardiac muscle. Pflugers Arch. 1991 Oct;419(3-4):310–318. doi: 10.1007/BF00371112. [DOI] [PubMed] [Google Scholar]
- Martyn D. A., Gordon A. M. Force and stiffness in glycerinated rabbit psoas fibers. Effects of calcium and elevated phosphate. J Gen Physiol. 1992 May;99(5):795–816. doi: 10.1085/jgp.99.5.795. [DOI] [PMC free article] [PubMed] [Google Scholar]
- McKillop D. F., Fortune N. S., Ranatunga K. W., Geeves M. A. The influence of 2,3-butanedione 2-monoxime (BDM) on the interaction between actin and myosin in solution and in skinned muscle fibres. J Muscle Res Cell Motil. 1994 Jun;15(3):309–318. doi: 10.1007/BF00123483. [DOI] [PubMed] [Google Scholar]
- McKillop D. F., Geeves M. A. Regulation of the interaction between actin and myosin subfragment 1: evidence for three states of the thin filament. Biophys J. 1993 Aug;65(2):693–701. doi: 10.1016/S0006-3495(93)81110-X. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Metzger J. M., Moss R. L. Calcium-sensitive cross-bridge transitions in mammalian fast and slow skeletal muscle fibers. Science. 1990 Mar 2;247(4946):1088–1090. doi: 10.1126/science.2309121. [DOI] [PubMed] [Google Scholar]
- Metzger J. M., Moss R. L. Kinetics of a Ca(2+)-sensitive cross-bridge state transition in skeletal muscle fibers. Effects due to variations in thin filament activation by extraction of troponin C. J Gen Physiol. 1991 Aug;98(2):233–248. doi: 10.1085/jgp.98.2.233. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Metzger J. M., Moss R. L. Myosin light chain 2 modulates calcium-sensitive cross-bridge transitions in vertebrate skeletal muscle. Biophys J. 1992 Aug;63(2):460–468. doi: 10.1016/S0006-3495(92)81614-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Millar N. C., Homsher E. The effect of phosphate and calcium on force generation in glycerinated rabbit skeletal muscle fibers. A steady-state and transient kinetic study. J Biol Chem. 1990 Nov 25;265(33):20234–20240. [PubMed] [Google Scholar]
- Pate E., Franks-Skiba K., White H., Cooke R. The use of differing nucleotides to investigate cross-bridge kinetics. J Biol Chem. 1993 May 15;268(14):10046–10053. [PubMed] [Google Scholar]
- Regnier M., Martyn D. A., Chase P. B. Calcium regulation of tension redevelopment kinetics with 2-deoxy-ATP or low [ATP] in rabbit skeletal muscle. Biophys J. 1998 Apr;74(4):2005–2015. doi: 10.1016/S0006-3495(98)77907-X. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Regnier M., Martyn D. A., Chase P. B. Calmidazolium alters Ca2+ regulation of tension redevelopment rate in skinned skeletal muscle. Biophys J. 1996 Nov;71(5):2786–2794. doi: 10.1016/S0006-3495(96)79471-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Regnier M., Morris C., Homsher E. Regulation of the cross-bridge transition from a weakly to strongly bound state in skinned rabbit muscle fibers. Am J Physiol. 1995 Dec;269(6 Pt 1):C1532–C1539. doi: 10.1152/ajpcell.1995.269.6.C1532. [DOI] [PubMed] [Google Scholar]
- Sweeney H. L., Stull J. T. Alteration of cross-bridge kinetics by myosin light chain phosphorylation in rabbit skeletal muscle: implications for regulation of actin-myosin interaction. Proc Natl Acad Sci U S A. 1990 Jan;87(1):414–418. doi: 10.1073/pnas.87.1.414. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wahr P. A., Cantor H. C., Metzger J. M. Nucleotide-dependent contractile properties of Ca(2+)-activated fast and slow skeletal muscle fibers. Biophys J. 1997 Feb;72(2 Pt 1):822–834. doi: 10.1016/s0006-3495(97)78716-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Walker J. W., Lu Z., Moss R. L. Effects of Ca2+ on the kinetics of phosphate release in skeletal muscle. J Biol Chem. 1992 Feb 5;267(4):2459–2466. [PubMed] [Google Scholar]
- White H. D., Belknap B., Jiang W. Kinetics of binding and hydrolysis of a series of nucleoside triphosphates by actomyosin-S1. Relationship between solution rate constants and properties of muscle fibers. J Biol Chem. 1993 May 15;268(14):10039–10045. [PubMed] [Google Scholar]