Abstract
Substitution of any of a variety of organic anions, including acetate, propionate, lactate, gluconate, and succinate, for chloride in the reactivation medium improves the motility of demembranated sperm of Tripneustes gratilla. At the optimum concentration of 0.20 N, all of these anions improve the duration of motility, with lactate and gluconate being the best. The Michaelis constant for beat frequency (Kmf) is lower (0.11-0.14 mM at 22 degrees C) in most of the organic anions than it is in Cl- (0.20 mM), and the minimum ATP concentration required to support oscillatory beating is reduced from 10 microM in chloride to 2 microM in acetate, which together indicate a greater affinity of the axonemal ATPase for MgATP2- in the organic anions media. The maximal beat frequency, fmax, is as high as 42 Hz in 0.2 N succinate compared to 31 Hz in Cl-, whereas the mean bend angle averages 2.8 rad in acetate compared to 2.4 rad in Cl-; these values give a calculated average velocity of tubule sliding of approximately 15 micron/s in acetate and succinate, which is approximately 30% greater than the value of 11 micron/s observed in chloride. The reactivated sperm are sixfold more sensitive to vanadate inhibition in 0.2 M acetate than they are in 0.15 M Cl-. The specific ATPase activity of soluble dynein 1, which increases more than 15-fold between 0 and 1.0 N Cl-, undergoes only a twofold activation over the same range of organic anion concentration, and, like the reactivated motility, is up to 50-fold more sensitive to vanadate. This greater apparent mechanochemical efficiency and the increased sensitivity to vanadate inhibition in the organic anions suggest that they, unlike chloride, do not promote the spontaneous dissociation of ADP and PO4(3-) from the dynein-ADP-PO4 kinetic intermediate in the dynein crossbridge cycle. The use of organic anion media may lead to significant improvements in reactivation of other motile and transport systems.
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- Beckerle M. C., Porter K. R. Inhibitors of dynein activity block intracellular transport in erythrophores. Nature. 1982 Feb 25;295(5851):701–703. doi: 10.1038/295701a0. [DOI] [PubMed] [Google Scholar]
- Bell C. W., Fraser C., Sale W. S., Tang W. J., Gibbons I. R. Preparation and purification of dynein. Methods Cell Biol. 1982;24:373–397. doi: 10.1016/s0091-679x(08)60666-4. [DOI] [PubMed] [Google Scholar]
- Bessen M., Fay R. B., Witman G. B. Calcium control of waveform in isolated flagellar axonemes of Chlamydomonas. J Cell Biol. 1980 Aug;86(2):446–455. doi: 10.1083/jcb.86.2.446. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Brenner B., Yu L. C., Podolsky R. J. X-ray diffraction evidence for cross-bridge formation in relaxed muscle fibers at various ionic strengths. Biophys J. 1984 Sep;46(3):299–306. doi: 10.1016/S0006-3495(84)84026-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Brokaw C. J. Activation and reactivation of Ciona spermatozoa. Prog Clin Biol Res. 1982;80:185–189. doi: 10.1002/cm.970020735. [DOI] [PubMed] [Google Scholar]
- Brokaw C. J., Benedict B. Mechanochemical coupling in flagella. I. Movement-dependent dephosphorylation of ATP by glycerinated spermatozoa. Arch Biochem Biophys. 1968 Jun;125(3):770–778. doi: 10.1016/0003-9861(68)90513-4. [DOI] [PubMed] [Google Scholar]
- Brokaw C. J. Calcium-induced asymmetrical beating of triton-demembranated sea urchin sperm flagella. J Cell Biol. 1979 Aug;82(2):401–411. doi: 10.1083/jcb.82.2.401. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Brokaw C. J. Effects of viscosity and ATP concentration on the movement of reactivated sea-urchin sperm flagella. J Exp Biol. 1975 Jun;62(3):701–719. doi: 10.1242/jeb.62.3.701. [DOI] [PubMed] [Google Scholar]
- Brokaw C. J., Josslin R., Bobrow L. Calcium ion regulation of flagellar beat symmetry in reactivated sea urchin spermatozoa. Biochem Biophys Res Commun. 1974 Jun 4;58(3):795–800. doi: 10.1016/s0006-291x(74)80487-0. [DOI] [PubMed] [Google Scholar]
- Brokaw C. J., Nagayama S. M. Modulation of the asymmetry of sea urchin sperm flagellar bending by calmodulin. J Cell Biol. 1985 Jun;100(6):1875–1883. doi: 10.1083/jcb.100.6.1875. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Buckley I., Stewart M. Ciliary but not saltatory movements are inhibited by vanadate microinjected into living cultured cells. Cell Motil. 1983;3(2):167–184. doi: 10.1002/cm.970030206. [DOI] [PubMed] [Google Scholar]
- Cande W. Z., Wolniak S. M. Chromosome movement in lysed mitotic cells is inhibited by vanadate. J Cell Biol. 1978 Nov;79(2 Pt 1):573–580. doi: 10.1083/jcb.79.2.573. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Clark T. G., Rosenbaum J. L. Pigment particle translocation in detergent-permeabilized melanophores of Fundulus heteroclitus. Proc Natl Acad Sci U S A. 1982 Aug;79(15):4655–4659. doi: 10.1073/pnas.79.15.4655. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Forman D. S. Vanadate inhibits saltatory organelle movement in a permeabilized cell model. Exp Cell Res. 1982 Sep;141(1):139–147. doi: 10.1016/0014-4827(82)90076-3. [DOI] [PubMed] [Google Scholar]
- Gibbons B. H. Effects of organic solvents on flagellar asymmetry and quiescence in sea urchin sperm. J Cell Sci. 1982 Apr;54:115–135. doi: 10.1242/jcs.54.1.115. [DOI] [PubMed] [Google Scholar]
- Gibbons B. H., Gibbons I. R. Calcium-induced quiescence in reactivated sea urchin sperm. J Cell Biol. 1980 Jan;84(1):13–27. doi: 10.1083/jcb.84.1.13. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gibbons B. H., Gibbons I. R. Flagellar movement and adenosine triphosphatase activity in sea urchin sperm extracted with triton X-100. J Cell Biol. 1972 Jul;54(1):75–97. doi: 10.1083/jcb.54.1.75. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gibbons B. H., Gibbons I. R. Properties of flagellar "rigor waves" formed by abrupt removal of adenosine triphosphate from actively swimming sea urchin sperm. J Cell Biol. 1974 Dec;63(3):970–985. doi: 10.1083/jcb.63.3.970. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gibbons B. H., Gibbons I. R. Relationship between the latent adenosine triphosphatase state of dynein 1 and its ability to recombine functionally with KCl-extracted sea urchin sperm flagella. J Biol Chem. 1979 Jan 10;254(1):197–201. [PubMed] [Google Scholar]
- Gibbons B. H. Reactivation of sperm flagella: properties of microtubules-mediated motility. Methods Cell Biol. 1982;25(Pt B):253–271. [PubMed] [Google Scholar]
- Gibbons I. R., Cosson M. P., Evans J. A., Gibbons B. H., Houck B., Martinson K. H., Sale W. S., Tang W. J. Potent inhibition of dynein adenosinetriphosphatase and of the motility of cilia and sperm flagella by vanadate. Proc Natl Acad Sci U S A. 1978 May;75(5):2220–2224. doi: 10.1073/pnas.75.5.2220. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gibbons I. R., Evans J. A., Gibbons B. H. Acetate anions stabilize the latency of dynein 1 ATPase and increase the velocity of tubule sliding in reactivated sperm flagella. Prog Clin Biol Res. 1982;80:181–184. doi: 10.1002/cm.970020734. [DOI] [PubMed] [Google Scholar]
- Gibbons I. R., Fronk E. A latent adenosine triphosphatase form of dynein 1 from sea urchin sperm flagella. J Biol Chem. 1979 Jan 10;254(1):187–196. [PubMed] [Google Scholar]
- Gibbons I. R., Fronk E. Some properties of bound and soluble dynein from sea urchin sperm flagella. J Cell Biol. 1972 Aug;54(2):365–381. doi: 10.1083/jcb.54.2.365. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gibbons I. R., Gibbons B. H. Transient flagellar waveforms during intermittent swimming in sea urchin sperm. I. Wave parameters. J Muscle Res Cell Motil. 1980 Mar;1(1):31–59. doi: 10.1007/BF00711924. [DOI] [PubMed] [Google Scholar]
- Goldstein S. F. Form of developing bends in reactivated sperm flagella. J Exp Biol. 1976 Feb;64(1):173–184. doi: 10.1242/jeb.64.1.173. [DOI] [PubMed] [Google Scholar]
- Goodenough U. W. Motile detergent-extracted cells of Tetrahymena and Chlamydomonas. J Cell Biol. 1983 Jun;96(6):1610–1621. doi: 10.1083/jcb.96.6.1610. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hamel E., Lin C. M. Glutamate-induced polymerization of tubulin: characteristics of the reaction and application to the large-scale purification of tubulin. Arch Biochem Biophys. 1981 Jun;209(1):29–40. doi: 10.1016/0003-9861(81)90253-8. [DOI] [PubMed] [Google Scholar]
- Hamel E., del Campo A. A., Lowe M. C., Waxman P. G., Lin C. M. Effects of organic acids on tubulin polymerization and associated guanosine 5'-triphosphate hydrolysis. Biochemistry. 1982 Feb 2;21(3):503–509. doi: 10.1021/bi00532a014. [DOI] [PubMed] [Google Scholar]
- Hyams J. S., Borisy G. G. Isolated flagellar apparatus of Chlamydomonas: characterization of forward swimming and alteration of waveform and reversal of motion by calcium ions in vitro. J Cell Sci. 1978 Oct;33:235–253. doi: 10.1242/jcs.33.1.235. [DOI] [PubMed] [Google Scholar]
- Johnson K. A. Pathway of the microtubule-dynein ATPase and the structure of dynein: a comparison with actomyosin. Annu Rev Biophys Biophys Chem. 1985;14:161–188. doi: 10.1146/annurev.bb.14.060185.001113. [DOI] [PubMed] [Google Scholar]
- Johnson K. A. The pathway of ATP hydrolysis by dynein. Kinetics of a presteady state phosphate burst. J Biol Chem. 1983 Nov 25;258(22):13825–13832. [PubMed] [Google Scholar]
- Kobayashi T., Martensen T., Nath J., Flavin M. Inhibition of dynein ATPase by vanadate, and its possible use as a probe for the role of dynein in cytoplasmic motility. Biochem Biophys Res Commun. 1978 Apr 28;81(4):1313–1318. doi: 10.1016/0006-291x(78)91279-2. [DOI] [PubMed] [Google Scholar]
- LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
- Naito Y., Kaneko H. Reactivated triton-extracted models o paramecium: modification of ciliary movement by calcium ions. Science. 1972 May 5;176(4034):523–524. doi: 10.1126/science.176.4034.523. [DOI] [PubMed] [Google Scholar]
- Okuno M. Inhibition and relaxation of sea urchin sperm flagella by vanadate. J Cell Biol. 1980 Jun;85(3):712–725. doi: 10.1083/jcb.85.3.712. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Omoto C. K., Brokaw C. J. Structure and behaviour of the sperm terminal filament. J Cell Sci. 1982 Dec;58:385–409. doi: 10.1242/jcs.58.1.385. [DOI] [PubMed] [Google Scholar]
- Porter M. E., Johnson K. A. Transient state kinetic analysis of the ATP-induced dissociation of the dynein-microtubule complex. J Biol Chem. 1983 May 25;258(10):6582–6587. [PubMed] [Google Scholar]
- Sale W. S., Gibbons I. R. Study of the mechanism of vanadate inhibition of the dynein cross-bridge cycle in sea urchin sperm flagella. J Cell Biol. 1979 Jul;82(1):291–298. doi: 10.1083/jcb.82.1.291. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Shimizu T., Johnson K. A. Presteady state kinetic analysis of vanadate-induced inhibition of the dynein ATPase. J Biol Chem. 1983 Nov 25;258(22):13833–13840. [PubMed] [Google Scholar]
- Stommel E. W., Stephens R. E., Alkon D. L. Motile statocyst cilia transmit rather than directly transduce mechanical stimuli. J Cell Biol. 1980 Dec;87(3 Pt 1):652–662. doi: 10.1083/jcb.87.3.652. [DOI] [PMC free article] [PubMed] [Google Scholar]
- TAUSSKY H. H., SHORR E. A microcolorimetric method for the determination of inorganic phosphorus. J Biol Chem. 1953 Jun;202(2):675–685. [PubMed] [Google Scholar]
- WILKINSON G. N. Statistical estimations in enzyme kinetics. Biochem J. 1961 Aug;80:324–332. doi: 10.1042/bj0800324. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wais-Steider J., Satir P. Effect of vanadate on gill cilia: switching mechanism in ciliary beat. J Supramol Struct. 1979;11(3):339–347. doi: 10.1002/jss.400110309. [DOI] [PubMed] [Google Scholar]